- Research article
- Open Access
- Open Peer Review
Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium
BMC Medical Genomics volume 12, Article number: 149 (2019)
Genetics play an important role in intracranial aneurysm (IA) pathophysiology. Genome-wide association studies have identified several single nucleotide polymorphisms (SNPs) that are linked to IA but how they affect disease pathobiology remains poorly understood. We used Encyclopedia of DNA Elements (ENCODE) data to investigate the epigenetic landscapes surrounding genetic risk loci to determine if IA-associated SNPs affect functional elements that regulate gene expression and if those SNPs are most likely to impact a specific type of cells.
We mapped 16 highly significant IA-associated SNPs to linkage disequilibrium (LD) blocks within the human genome. Within these regions, we examined the presence of H3K4me1 and H3K27ac histone marks and CCCTC-binding factor (CTCF) and transcription-factor binding sites using chromatin immunoprecipitation-sequencing (ChIP-Seq) data. This analysis was conducted in several cell types relevant to endothelial (human umbilical vein endothelial cells [HUVECs]) and inflammatory (monocytes, neutrophils, and peripheral blood mononuclear cells [PBMCs]) biology. Gene ontology analysis was performed on genes within extended IA-risk regions to understand which biological processes could be affected by IA-risk SNPs. We also evaluated recently published data that showed differential methylation and differential ribonucleic acid (RNA) expression in IA to investigate the correlation between differentially regulated elements and the IA-risk LD blocks.
The IA-associated LD blocks were statistically significantly enriched for H3K4me1 and/or H3K27ac marks (markers of enhancer function) in endothelial cells but not in immune cells. The IA-associated LD blocks also contained more binding sites for CTCF in endothelial cells than monocytes, although not statistically significant. Differentially methylated regions of DNA identified in IA tissue were also present in several IA-risk LD blocks, suggesting SNPs could affect this epigenetic machinery. Gene ontology analysis supports that genes affected by IA-risk SNPs are associated with extracellular matrix reorganization and endopeptidase activity.
These findings suggest that known genetic alterations linked to IA risk act on endothelial cell function. These alterations do not correlate with IA-associated gene expression signatures of circulating blood cells, which suggests that such signatures are a secondary response reflecting the presence of IA rather than indicating risk for IA.
Intracranial aneurysms (IAs) are characterized by aberrant gene expression consistent with inflammatory cell infiltration and immune cell-regulated vascular degeneration [1,2,3,4,5]. The presence of abnormal transcriptional signatures in the peripheral blood of patients with IAs has also been observed in several recently published reports [6,7,8,9,10]. In a case-controlled study, we performed transcriptome profiling of circulating neutrophils in patients with and without IAs . Differential expression analysis revealed statistically significant differentially expressed transcripts that were related to increased peripheral neutrophil activation. These findings led us to question whether the aberrant peripheral blood gene expression signatures are the result of an interaction between these circulating neutrophils and the diseased aneurysmal tissue or whether the formation of the aneurysm is due to dysregulated immune or inflammatory processes that might be attributed partly to genetics.
Genetics play an important role in IA pathophysiology. Patients with certain hereditary diseases (i.e., Ehlers-Danlos syndrome, Marfan syndrome, Neurofibromatosis-1) are known to have higher rates of IAs (10–20%) and aneurysm rupture (8–25%) compared to the general population . Many mutations associated with these conditions (e.g., collagen [COL1A1] in patients with Ehlers-Danlos syndrome) affect the structural integrity of the vasculature or the ability of the vessel walls to maintain homeostasis [12, 13]. A family history of IA is also associated with higher IA prevalence (10%) and rupture rates (4%) , suggesting other heritable genetic factors contribute to disease susceptibility. Genome-wide association studies (GWAS) using large cohorts from principally Dutch, Finnish, and Japanese populations have identified many single nucleotide polymorphisms (SNPs) that occur more commonly in individuals with IAs [15,16,17,18,19,20,21,22,23]. In these studies, significant associations were reported at 2q32.1 (PLCL1) , 8q11.23–q12.1 (SOX17) , 9p21.3 (CDKN2A-CDKN2B) , 18q11.2 (RBBP8) , 13q13.1 (STARD13) , and 10q24.32.12 . The most frequently replicated locus has been 9p21.3 at the noncoding RNA, CDKN2B–AS1, which is in the CDKN2B-CDKN2A gene cluster, and has been shown to be a significant genetic susceptibility locus for cardiovascular diseases . In a meta-analysis, Alg et al.  investigated 66 case-controlled studies that included 32,887 IA patients and 83,683 control subjects and identified 19 SNPs that were significantly associated with IAs, the most replicated of which were at 9p21.3, 8q11, and 4q31.23. Like those in association with other complex diseases or traits [26,27,28,29], several IA-risk loci have been found in noncoding regions of the genome, suggesting that genetic risk may operate on functional regulatory elements that influence gene expression, rather than on the structure of the gene product .
The overall objective of this study was to gain insights into the pathobiology of IA by examining the chromatin features in genetic regions known to confer risk for aneurysm within pathologically relevant cells. Our secondary objective was to determine if genetic variation in any of these regions could affect gene expression differences reported in our previous neutrophil transcriptome profiling study . To do this, we investigated IA-associated genetic risk loci (validated in at least two studies) reported by the meta-analysis by Alg et al.  to determine if they contained (A) functional, regulatory elements, such as histone modifications; (B) genes that are relevant to vascular and immune or inflammatory function that could be involved in IA; and (C) differentially expressed genes identified in our previous study . To investigate the epigenetic effects of SNPs in specific cell types, in this study, we separately examined the loci in human umbilical vein endothelial cells (HUVECs), monocytes, neutrophils, and peripheral blood mononuclear cells (PBMCs) using data available from the Encyclopedia of DNA Elements (ENCODE) project . Specifically, we assessed the presence of H3K4me1/H3K27ac histone marks, CCCTC-binding factor (CTCF) sites, and transcription-factor binding sites (TFBSs). Furthermore, we examined whether genetic variation might impact other epigenetic features, such as DNA methylation, by querying DNA methyl-seq data collected by Yu et al. and if genetic variation could affect gene expression differences reported in the aneurysmal tissue in Yu et al. and circulating immune cells reported by Tutino et al. [6, 32].
Defining LD blocks
The identities of IA-risk SNPs were obtained from a comprehensive, published meta-analysis by Alg et al. , which evaluated 66 case-controlled studies and identified 19 significant IA-associated SNPs . Importantly, all 19 identified SNPs had been reported as significantly associated with IA in two or more publications. We note, however, that these publications did not all make a distinction of whether the IAs were saccular or fusiform, and thus the 19 SNPs may be related to either type of IA, or both.
It should be noted that SNPs identified on GWAS do not identify the causal polymorphism; rather, they index a larger genetic region where risk may operate, and thus the causal SNP may be anywhere within the LD block. For this reason, it was critical for us to examine the haplotype blocks surrounding the index SNPs of interest. The SNP Annotation and Proxy (SNAP) search tool  and the proxy search within Single Nucleotide Polymorphisms Annotator (SNiPA) tool were used to identify linkage disequilibrium (LD) (haplotype) blocks associated with each SNP. We used the following settings for SNAP: SNP dataset – 1000 genome pilot 1 and HapMap3 (release 2); r2 threshold – 0.9; population panel – CEU; distance limit – 500. And the following settings for SNiPA: genome assembly – GRCh37; variant set – 1000 Genomes; population – American; genome annotation – Ensembl 87; r2 threshold – 0.9. The smallest and largest genomic positions were used as the start and stop locations, respectively, for each LD block.
Identification of H3K4me1/H3K27ac histone marks within LD blocks
We queried genomic regions that might have enhancer function by identifying H3K4me1 and H3K27ac histone marks . ENCODE data was used for genomic locations of H3K4me1/H3K27ac marks in HUVECs, monocytes (CD14+ RO01746), and peripheral blood mononuclear cells (only H3K4me1 data were available). We used H3K4me1/H3k27ac ChIP-Seq data from healthy adult neutrophils reported by Jiang et al.  to find H3K4me1/H3K27ac genomic locations in neutrophils (GEO:GSE66896). ENCODE histone data were downloaded from the University of California Santa Cruz Genome Browser ENCODE database  with the following accession numbers: HUVECs H3K4me1 GSM733690, HUVECs H3K27ac GSM733691, monocytes H3K4me1 GSM1003535, monocytes H3K27ac GSM1003559, and PBMCs H3K4me1 GSM788084.
To identify the intersection of H3K4me1/H3K27ac peaks within LD regions, we used the BEDTools software intersect command , following the procedure established in Jiang et al. . In brief, 10,000 random regions in the human genome of the average length (32,312 bp) of SNAP assessed IA LD blocks were generated in BEDTools using the random intersect command. BEDTools intersect was used to determine (a) the number of LD regions that overlap with histone peaks, (b) the number of random regions that overlap with histone peaks, (c) the number of LD regions that do not overlap with histone peaks, and (d) the number of random regions that do not overlap with histone peaks. To determine whether H3K4me1/H3K27ac marks within IA LD blocks occurred at a statistically-greater-than-expected frequency, we performed a Fisher’s exact test (p-value< 0.05 was considered significant).
Identification of CTCF binding sites within LD blocks
We investigated CTCF sites within IA-risk LD blocks using ENCODE data for HUVECs and monocytes (data not available for other cell types) as an indicator of chromatin organization that could affect gene expression. CTCF data were downloaded under the following accession numbers: HUVECs GSM733716, monocytes GSM1003508. As conducted for histone marks, BEDTools intersect was used to determine the intersection of binding sites within LD regions and randomly generated regions. A p-value< 0.05 (Fisher’s exact test) was used to determine LD regions with significant CTCF sites.
Identification of TF binding sites within LD blocks
An important feature of functional elements in the noncoding genome (including enhancers) is the presence of multiple TFBSs within LD blocks. To determine whether H3K4me1/H3K27ac-marked regions were functional, we assessed the presence of TF binding sites within these regions. HUVECs were the only cell type considered because they were the only ones to have significant histone modifications in the IA-risk LD blocks. All TFs with data available for HUVECs within the ENCODE data sets were considered. Binding sites for EZH2, FOS, GATA2, JUN, MAX, MYC, POLR2A transcription factors were queried within the histone-marked locations of the IA-associated LD blocks. ENCODE data were downloaded for the following accession numbers: EZH2 wgEncodeEH003084; FOS wgEncodeEH001774; GATA2 wgEncodeEH001758; JUN wgEncodeEH000719; MAX wgEncodeEH000768; MYC wgEncodeEH000561; POLR2A wgEncodeEH000061, wgEncodeEH000552, wgEncodeEH000702, wgEncodeEH002297, wgEncodeEH002298. Sites were defined as “promoters” if they fell within 5 kb upstream or 1 kb downstream of the transcription start site; sites outside that window were considered distal. The transcription start site used to define TF as a promoter or distal site was provided by Switchgear Genomics on the University of California Santa Cruz Genome Browser .
Identifying molecular pathways of genes within extended LD regions
Genes that fell within 200 kb upstream or downstream of the IA-associated SNPs were input to the Database for Annotation, Visualization and Integrated Discovery (DAVID) [39, 40] (https://david.ncifcrf.gov/home.jsp, accessed March 2019). This tool uses a large knowledge base to identify associated biological processes and pathways for given sets of genes. We used the default settings for our analysis. We also implemented an alternative method of gene ontology analysis via the Gene Ontology Term Finder (GO::TermFinder)  (https://go.princeton.edu/cgi-bin/GOTermFinder, accessed March 2019). We used genes that fell within 200 kb upstream or downstream of the IA-risk SNPs as the input gene list. GO::TermFinder assessed whether the input gene list was enriched for any specific gene ontology term to a greater degree than what would be expected by chance (q-value< 0.05). Default settings for GO::TermFinder were used to generate molecular function, biological process, and cellular component ontologies.
Analysis of differential methylation and gene expression within LD blocks
We also evaluated genetic regulation of gene expression using DNA methylation data produced in the study conducted by Yu et al. , which is reported under the accession number of GSE75434. These authors compared DNA methylation within IA tissue samples to superficial temporal artery (STA) tissue from the same individual using the Infinium HumanMethylation450 BeadChip Kit (Illumina, San Diego, California). We determined whether any of these differentially methylated regions overlapped with the IA-risk LD blocks.
Yu et al.  also characterized the gene expression profiles of these IA and STA tissue samples using the Human Genome U133 Plus 2.0 GeneChip microarray (Affymetrix, Santa Clara, California). Raw microarray data, available under the accession number of GSE75436, were normalized by applying robust multichip average (RMA) normalization  in R with STA as control group. Genes with a fold-change of > 2 and a false discovery rate (FDR) of < 0.05 (after applying John Storey multiple hypothesis correction  to p-values calculated by an F-test of control and IA groups) were considered to be differentially expressed genes (DEGs). We identified the chromosomal locations for these genes in R using the human genome library , which draws from NCBI’s Entrez Gene database (https://www.ncbi.nlm.nih.gov/gene) and determined whether any of these genes fell within any of the IA-associated LD blocks (identified from Alg et al. ). Similarly, we examined the set of differentially expressed genes (p-value< 0.05, fold-change≥2) identified in our previous study that compared gene expression of circulating neutrophils from individuals with and without IAs (GSE106520) . We evaluated whether there was agreement between those differentially expressed genes and the IA-risk LD blocks.
For all three data sets of interest (Yu et al.  methylation, Yu et al.  gene expression, and Tutino et al.  gene expression) the intersect command of BEDTools was used to determine whether any overlap existed between IA-risk LD blocks and the regions of interest generated from these additional data sets. The random regions that approximate background genome previously used to assess the significance of histone marks and CTCF sites were again used to determine significance of any overlap with regions of interest. A p-value< 0.05 (Fisher’s exact test) was used to determine significance.
Queried LD blocks
From the 19 IA-risk SNPs identified in a comprehensive meta-analysis by Alg et al. , we were able to identify LD blocks for 16 of these SNPs, as given in Table 1. For the remaining 3 SNP loci (9p21.3 rs1333040, CSPG2 rs173686, ACE I/D), there was insufficient information available through SNAP search tool to assess linkage disequilibrium blocks. As evident in Table 1, the majority (11) of the IA-associated SNPs fall within non-coding regions of the genome, which is typical of complex traits. There are 4 SNPs within the set we examined that fall within an exon; however, this does not necessarily mean that the SNPs alter the coding function of that gene .
Location of H3K4me1/H3K27ac marks within LD blocks
To evaluate evidence of enhancer function within the IA-risk LD blocks, we used ENCODE data to determine whether H3K4me1 and H3K27ac marks expressed in HUVECs (relevant to endothelial biology) or monocytes, neutrophils, and PBMCs (relevant to inflammatory biology) were enriched within the LD blocks, compared to the genome background. HUVECs exhibited the greatest number of histone marks within the IA-risk LD blocks as compared to the randomly generated regions that represent the background genome. Table 2 shows that H3K4me1 enrichment was found in 15 blocks, while 10 of those blocks also exhibited H3K27ac marks. Both H3K4me1 and H3K27ac marks were statistically significantly enriched in LD blocks when compared to the genome background as assessed by Fisher’s exact test (p = 4.7E-05, p = 0.012; respectively). When we examined neutrophil, monocyte, and PBMC data, we did not find significant enrichment for H3K4me1 or H3K27ac marks within the IA-associated risk loci above the background genome levels.
Figure 1 shows the landscape around the SNP, rs1800255, within the 30th exon of the collagen type III alpha chain (COL3A1). This gene encodes for components of type III collagen, an integral component of blood vessel walls. Mutations in this gene are known to cause the vascular type of Ehlers-Danlos syndrome (type IV), a genetic disease affecting connective tissue. Ehlers-Danlos syndrome is associated with increased presence of IA; 12% of those with Ehlers-Danlos have IA , which is approximately double the rate of that in the general population . Furthermore, only ECs express histone marks in this LD block, indicated by the green box. In this LD block, it is unclear whether the genetic risk operates through the protein-coding gene or through enhancer activity within the ECs. Figure 2 shows the landscape of the LD block containing rs10958409, an intergenic SNP; note that there are no protein-coding genes within this haplotype. In this LD block, as in Fig. 1, we note that only the ECs show enrichment for H3K4me1/H3K27ac histone marks (green box). In this case, it is likely that genetic risk impinges on the endothelium by enhancer regulation.
CTCF binding sites within LD blocks
CTCF is an important regulator of three-dimensional chromatin architecture and therefore gene expression [48, 49]. We investigated if CTCF binding sites were present in HUVECs and monocytes within the IA-risk LD blocks (CTCF binding site data was not available for neutrophils or PBMCs). As shown in Table 3, HUVECs exhibited CTCF binding sites within 10 LD blocks, 8 of which also had both H3K4me1 and H3K27ac histone marks (see also Table 2). CTCF binding sites were found in 7 LD blocks for monocytes, 5 of which corresponded to blocks with both histone marks (see also Table 2). The frequency of CTCF binding sites within LD blocks was not significantly greater than the frequency of CTCF binding sites within the randomly generated regions (Fisher’s exact test). In Figs. 1a and 2a, we noticed CTCF sites within the IA-associated LD blocks (first 3 rows within the blue box).
TF binding sites within histone marks of HUVEC LD blocks
Although the H3K4me1 and H3K27ac histone marks suggest poised and active enhancers, respectively, a TFBS within the histone-marked regions that fall within the IA-associated LD blocks strongly indicates that the region is functional and can ultimately transcribe RNA . Because the IA-associated LD blocks were enriched for H3K4me1/H3K27ac marks just in HUVECs, we only examined TFBSs in the histone-marked sections for HUVECs. We examined all transcription factors with data available for HUVECs in ENCODE. Figure 1a and Fig. 2a also provide examples of TFBS that fall within the histone-marked regions (blue box). Binding sites for EZH2, FOS, GATA2, JUN, MAX, MYC, and/or POLR2A were present within the H3K4me1/H3K27ac-marked regions as shown in Table 4.
Table 4 also shows the location of the TFBS with respect to the transcription start site and promoter or distal elements. Distal TFBSs may be involved in regulatory processes in regions other than promoters, such as intergenic regions where noncoding RNA is encoded . We noted significant TF binding in distal regions of the IA-associated LD blocks. There were distal TFBSs for FOS in 10 of the 16 LD blocks, for JUN in 9 of the 16 LD blocks, and for GATA2 in 7 of the 16 LD blocks. POLR2A had distal or promoter TFBSs in 6 of the 16 LD blocks. Furthermore, multiple TFBS were evident in the promoter regions within the IA-associated LD blocks. EZH2, MAX, MYC, and POLR2A were present in the promoter region for at least 1 of the LD blocks of interest. These TFs interact together and with another transcription factor (MAD) to activate or inhibit specific gene transcription and affect cell proliferation, differentiation, and death . The overlap of histone modifications and promoter TF binding sites within the IA-risk regions could suggest a complicated interaction between enhancers and promoters that can affect gene regulation.
Enriched molecular pathways of disease-associated SNPs
We used the DAVID database to identify significantly enriched biological ontology terms for the 67 protein-coding genes located ±200 kb from the IA-associated SNPs. Of these, 57 corresponded to DAVID IDs and were used in the classification. Twenty ontologies were identified as significant (Benjamini Hochberg-adjusted p-value < 0.05) using the functional annotation tool, as shown in Table 5. These ontologies were functionally related to the serpin family, extracellular matrix (ECM) organization, receptor interactions, and fibrillar collagen.
We also conducted gene ontology analysis using GO::TermFinder to identify significant (Benjamini Hochberg-adjusted p-value < 0.05) molecular processes, functions, and components enriched in the list of 67 genes. The significant molecular function terms and their associated p-values are shown in Fig. 3 (excluding “unannotated” terms). Significant biological functions, processes, and components included ontologies such as endopeptidase regulator activity, regulation of endopeptidase activity, ECM structural constituent, fibrillar collagen trimer, and complex of collagen trimers. The entire list of significant ontologies is presented in Additional file 1: Table S1. Flow diagrams of significant molecular processes and components are presented in Additional file 1: Figures S1 and S2, respectively.
Differential methylation and expression within LD blocks
To evaluate if differentially methylated regions could be affecting gene regulation within the IA-risk LD blocks, we compared the differentially methylated regions reported by Yu et al.  to those of the 16 identified LD blocks. Yu et al.  identified 11,022 differentially DNA methylated regions when they compared IA tissue samples and matched STA tissue samples. Table 6 reports the 4 differentially methylated sites that intersected with 3 LD blocks associated with risk for IA; however, this was not statistically significant when compared to intersections between differentially methylated regions and randomly-created background genome regions.
We also analyzed gene expression in vascular tissue to determine if the 16 LD blocks could affect the expression differences reported in the literature. To that end, data from two sources was used. First, we used the differential RNA expression data from IA tissue and matched STA tissue from Yu et al. . We generated a list of 596 significant probes (fold change> 2, FDR < 0.05), which corresponded to 516 gene transcripts. There was not sufficient data available through the Entrez database to determine the location for 40 of the transcripts; consequently, these transcripts were excluded from the analysis. Ultimately, 476 regions were input to BEDTools for comparison with IA-risk LD blocks. Only 1 gene, COL1A2, overlapped with the IA-risk blocks, and this result was not found to be statistically significant by Fisher’s exact test.
Secondly, we performed a similar analysis using RNA expression differences reported in inflammatory cells from our previous RNA sequencing study profiling circulating neutrophils of individuals with and without IA . Of the 82 genes that showed differential expression between patients with IA and those without, we were able to assess chromosomal positions for 76 transcripts. None of these 76 genes were located within the LD blocks associated with IA risk. This finding suggests that the IA-risk loci may (a) act on the coding sequences (and therefore function) of one or more of the genes within the haplotypes, (b) act by long-distance enhancer-promoter interactions, or (c) both.
In this study, we used ENCODE data to investigate epigenetic landscapes of 16 prominent IA risk haplotypes. Within these haplotype blocks, we found evidence that genetic alterations (i.e. SNPs) may affect transcription of genes relevant to IA development through modulation of enhancer activity. Our analyses showed that functional regulatory elements within the IA-associated risk regions were present to a greater degree in ECs than immune cells. This suggests that genetic risk for IA is more likely to be conferred through the ECs than immune cells. Differentially expressed transcripts that we previously identified in circulating neutrophils were not associated with the investigated LD blocks. Thus, the abnormal gene expression observed in circulating neutrophils may reflect the presence of the aneurysmal lesion, rather than genetic risk that could precede IA initiation.
Genetic risk in the endothelium of persons with IA
The 16 IA-associated LD blocks considered in this study not only contained coding genes, but also contained apparent enhancers in noncoding regions that were specifically enriched in ECs. The histone marks H3K4me1 and H3K27ac (associated with poised or active enhancer function) were seen exclusively in ECs. H3K4me1 and H3K27ac marks in the IA-associated haplotypes were present at a greater-than-expected frequency in HUVECs (p = 4.7E-05 for H3K4me1 marks, p = 0.012 for H3K27ac marks) but not in monocytes, neutrophils, or PBMCs.
In HUVECs, the H3K4me1/H3K27ac-marked sites also demonstrated abundant TFBSs, corroborating the idea that these noncoding regions are indeed functional regulatory elements. CTCF binding sites were present within the IA-associated LD blocks in HUVECs, although not in a greater-than-expected frequency (p = 0.066). These results suggest that genetic risk for IA is more likely to operate on a vascular component of the disease (i.e., ECs) rather than an immune component, because there was no enrichment for these functional features in immune cells.
Our bioinformatics analyses of the coding elements within or adjacent to the 16 IA-risk LD blocks also suggests that genetic risk affects the endothelium. DAVID analysis demonstrates ontological terms significantly associated with these genes to be “extracellular matrix,” “collagen,” “Ehlers-Danlos syndrome,” and “serpin.” Our GO::TermFinder results echo these findings; significant molecular functions of these genes were related to endopeptidase activity/regulation (SERPINA4, SERPINA3, SERPINA12, SERPINA9, SERPINA13P, SERPINA11, and SERPINA5) and ECM structural components (COL1A2, HAPLN1, VCAN, COL5A2, and COL3A1).
Our results implicate ECs as the cell type to most likely be affected by genetic risk. ECs have long been recognized as key players in IA pathogenesis . Animal models of IA initiation report that EC dysfunction is one of the first changes that correlate to aneurysm formation . This is likely because ECs dynamically react to aberrant hemodynamics that occur in locations where IAs preferentially form, i.e., at bifurcation apices and outer curves of tortuous arteries . Specifically, studies have shown that ECs react to increased wall shear stress by triggering signaling cascades that produce and activate proteases, namely matrix metalloproteinase (MMP)-2 and MMP-9, which damage the internal elastic lamina, cause smooth muscle cell (SMC) apoptosis, and weaken the vascular wall . We hypothesize that aberrant EC response mechanisms, potentially arising from the SNPs we investigated, could propagate pathological remodeling and consequently aneurysm formation and growth. Endothelial dysfunction, particularly in the breakdown of EC continuity, could lead to inflammatory responses, both within the vessel wall and in circulating cells, which are observed in IAs [56, 57].
A further examination of the genes within the 16 LD blocks also shows how genetic risk could affect fundamental pathobiological mechanisms in IAs. Remarkably, 4 of the SNPs in this study fall within exons of COL1A2, COL3A1, ribosome-binding protein 1 (RRBP1), and SERPINA3 and thus could exert their effects by directly changing the structure and/or function of the translated proteins. Polymorphisms in COL1A2 and COL3A1 (which together make up 80–90% of arterial collagens) are well-established in IAs [58, 59], and are known to lead to Ehlers-Danlos syndrome [13, 60, 61]. Production of defective collagens by ECs could contribute to impairment of the function and integrity of the endothelial layer during IA formation . However, because vascular SMCs produce COL1 and COL3 [63, 64], polymorphisms in the coding regions of these genes may reflect more extensive wall dysfunction due to their effect in vascular SMCs. SNPs in members of the serpin family could also affect ECM remodeling and stability, as they are inhibitors of serine proteases, which can degrade the matrix during IA formation . In an animal model contrasting ruptured and unruptured aneurysms, Kataoka et al.  found neutrophil-derived cathepsin G expressed in walls of ruptured aneurysms. The main inhibitory target of SERPINA3 is cathepsin G , which can activate pro-MMP-9  and contribute to ECM remodeling [69, 70]. Therefore, we suspect that the mutations in COL1A2, COL3A1, and SERPINA3 could lead to increased degradation and insufficient ECM repair during IA formation . Conversely, the exonic SNP in RRBP1, a ribosome receptor, may trigger a more universal defect in protein expression, as poor interactions between the ribosome and endoplasmic reticulum could negatively affect protein processing during IA development .
The remaining SNPs we studied fell within noncoding regions of the genome; and thus, the influence of the IA-risk SNP is likely felt through the modulation of enhancer activity, CTCF binding sites, or TFBSs. These SNPs could affect RNA expression by modulating the transcription machinery’s activity for genes within the haplotype. Our data demonstrate that genes potentially affected by the SNPs in noncoding regions may also be biologically relevant to IA pathogenesis. Genes affected by these SNPs could play a role in EC regulation of vascular remodeling and signaling during IA. For example, endothelin receptor type A (EDNRA) encodes for the receptor of endothelin-1, which through binding to the receptor leads to vasoconstriction during maintenance of vascular homeostasis . Endothelin-1 also stimulates inflammatory responses and proliferation [73,74,75], so altering the receptor EDNRA could also impact these key processes of aneurysmal remodeling. Additionally, ANKRD44 is a subunit of protein phosphatase 6, which can inhibit activation of NF-κB , an important pathway in pro-inflammatory EC signaling during IA pathogenesis . IL6, a proinflammatory cytokine, is secreted by both M1 macrophages  and lymphocytes  during IA formation and growth. Increased levels have been found in ruptured IAs during surgical clipping . Individuals with this polymorphism have higher IL6 plasma levels  and a higher risk of IA .
Interestingly, the analysis of methyl-seq data from Yu et al.  showed differential methylation in the LD blocks containing EDNRA and ANKRD44, suggesting that changes in their expression may be through an epigenetic mechanism. Additionally, alterations in the expression of genes such as VCAN and HSPG2, which encode proteins involved in cell adhesion, may affect the ability of circulating immune cells to adhere to the endothelium [83,84,85]. Several genes within the LD blocks of the SNPs that we studied (namely, CDKN2B-AS1, AGMO, BOLL, and FGD6) are not well characterized and warrant further investigation to determine how they may be associated with IA risk.
Relating these findings to previous studies
Although direct experimental investigation of epigenetic landscapes in IA has been sparse, in a recent study, Laarman et al.  performed ChIP-seq on DNA from postmortem human Circle of Willis tissue to identify histone H3K4me1 and H3K27ac modifications in regulatory regions (distal enhancers and active promoters). They then queried if these regions overlapped with 19 known IA-associated SNP regions (from [22, 23]) and found that 7 of them overlapped with active regulatory regions. Three of the SNPs they queried were also investigated in the current study, namely, rs1132274 (on chr20), rs6841581 (on chr4), and rs658595 (on chr12). Interestingly, rs6841581 was found by Laarman et al.  to likely affect TF binding while rs1132274 and rs653859 had minimal and no predicted TF activity, respectively. In a follow-up study, Laarman et al.  elegantly used chromatin conformation capture technology to identify enhancer targets of 4 known risk loci and confirmed intrinsic enhancer activity via an in vivo reporter assay. Two of the loci studied by Laarman et al. overlapped with those in our study, namely chr4:148365339–148,414,651 (rs6841584) and chr9:22077085–22,125,503 (rs10757278). These studies provide compelling experimental evidence of enhancer activity in regions reported in the present study, particularly for the SNPs mentioned above (rs6841584 and rs10757278). However, because Laarman et al. [86, 87] investigated DNA from multiple cell types (from whole Circle of Willis tissue), using their data to interpret our findings should be limited, pending confirmation through experimental validation in specific cell types, such as ECs, obtained from aneurysm tissue.
In addition to investigating if the chromatin landscape around IA-risk SNPs could inform us if aberrant transcriptomes detected in neutrophils precede or follow IA formation, we queried whether gene expression differences in recent aneurysm tissue studies could be related to the influence of SNPs within the 16 LD blocks. In a set of 516 differentially expressed genes between IA tissue and STA tissue taken from data published by Yu et al. , only COL1A2 fell within an LD block, pointing to the importance of functional collagen expression in the pathogenesis of IA. We may not have found overlap with any other DEGs and the IA-associated LD blocks because the data derived from Yu et al.  came from RNA samples from whole tissue and not cell-line ENCODE data. Thus, others cells, (i.e. SMCs, inflammatory cells, fibroblasts) may contribute to the expression differences determined from tissue samples and add significant noise to the data. In the future, laser micro-dissected sections of IA tissue could isolate ECs to better correlate expression differences with the epigenetic landscapes.
It is noteworthy that the IA-associated LD blocks did not contain any of the differentially expressed genes identified in our neutrophil RNA profiling study . This suggests that expression changes in circulating neutrophils during IA formation are a response to the existing aneurysmal lesion, rather than being an indication of IA risk. This is consistent with our published bioinformatics results , in which we found enriched leukocyte activation processes in the neutrophils, characterized by elevated levels of CD1D, CD7, CD86, CD177, and VNN1 antigens in patients with IA. This evidence led us to hypothesize that circulating neutrophils are activated in the bloodstream by contact with the diseased IA tissue [88,89,90] or with cytokines and chemokines thought to be released from the IA tissue .
In the present study, none of the IA-associated LD blocks were significantly enriched for histone marks or CTCF binding sites in neutrophils, which further supports our hypothesis. In fact, our results predict that functional regulatory elements in the IA-associated risk regions are present more in ECs, suggesting that genetic risk for IA is more likely to be conferred through the ECs than the immune cells. This is further supported by the Gene Ontology data demonstrating endopeptidase activity/regulation and ECM structural components, which may play significant roles in ECs, rather than immune cells (neutrophils). These results suggest that aberrant expression observed in circulating immune cells of individuals with IA is a secondary response following IA formation and not an indicator of genetic risk for the disease, at least for the 16 SNPs that we investigated. Therefore, the expression changes in circulating neutrophils that we observed could be caused by contact with inflamed aneurysm tissue or activation by chemokines and cytokines released from the aneurysm .
One limitation of this study is that we focused on IA-associated SNPs identified in a single comprehensive meta-analysis by Alg et al. , thus excluding SNPs that have been reported in other studies. However, the SNPs identified in the meta-analysis were found in at least 2 studies that analyzed a large volume of cases in controlled populations; consequently, these SNPs have a high likelihood of being associated with IA. Second, in this study, we focused on HUVECs, monocytes, neutrophils, and PBMCs and did not include data from other cells types, most notably vascular SMCs, which we recognize are critical to IA pathogenesis. Unfortunately, there was not sufficient cell-type specific ENCODE data available for vascular SMCs for use in our study. We also are assuming that the results from HUVECs generalize to endothelial cells derived from arterial-based aneurysms though it has been shown ECs in different tissues have distinct expression profiles . Third, we used genes within ±200 kb of IA associated SNPs for functional annotation and gene ontology analyses. However, it is likely that the relevant enhancers may regulate genes that are not within these regions, as demonstrated in the review by Kessler et al. . To identify genes affected by the enhancers we identified in this study, we would need to examine the topologically associated domains (TADs) of the IA associated risk SNPs. These domains may better describe which regions of the genome form interactions and thereby affect gene expression. We plan to study the TADs encompassing the IA-risk SNPs in the future. Lastly, we cannot be certain whether a specific genetic variant operates through the gene function in more complex landscapes that also include enhancer marks or TF binding. For instance, although a SNP may fall within an exon of a gene with biological significance in an IA, this region may also contain prominent H3K4me1/H3K27ac marks and function as a so-called “exonic enhancer” . In cases like this, the genetic variant could operate through the coding sequence function, the enhancer function, or both.
In this data-driven study, we analyzed 16 regions of known genetic risk for IAs that were identified by large GWAS and found that IA-risk SNPs were likely affecting the expression of genes relevant to IA development through modulation of enhancer activity. Using data from the ENCODE project, we were able to show that functional regulatory elements within the IA-associated risk regions were present to a greater degree in ECs compared to immune cells. Ontology analyses performed on genes potentially affected by each SNP showed cellular processes and functions related to regulation of ECM and protease. Although these findings do not exclude immune or inflammatory mediators as important elements in IA pathogenesis, they imply that known genetic risk factors for IA are more likely affecting the vessel wall than the circulating inflammatory cells. These results shed further light on how IA-associated SNPs may affect IA pathogenesis and highlight the importance of investigating noncoding elements in cell-type specific genomes. Our results also imply that the transcriptomic differences we have previously detected in circulating neutrophils are a response to the presence of the IA lesion, rather than an indication of risk for the disease.
Availability of data and materials
All datasets cited in this paper are publicly available. Links are provided within the manuscript text.
Collagen type I alpha 1 chain
Collagen type I alpha 2 chain
- COL3A1 :
Collagen type III alpha chain a
Collagen type V alpha 2 chain
Database for Annotation, Visualization and Integrated Discovery
Differentially expressed genes
- EDNRA :
Endothelin receptor type A
Encyclopedia of DNA Elements
Enhancer of zeste homolog 2
False discovery rate
Gene Ontology Term Finder
Genome-wide association studies
Human umbilical vein endothelial cells
MYC associated factor X
Peripheral blood mononuclear cells
RNA polymerase II
Robust multichip average
- RRBP1 :
Smooth muscle cell
SNP Annotation and Proxy
Single nucleotide polymorphism
Superficial temporal artery
Transcription factor binding site
Liu D, Han L, Wu X, Yang X, Zhang Q, Jiang F. Genome-wide microRNA changes in human intracranial aneurysms. BMC Neurol. 2014;14:188.
Shi C, Awad IA, Jafari N, Lin S, Du P, Hage ZA, et al. Genomics of human intracranial aneurysm wall. Stroke. 2009;40(4):1252–61.
Bekelis K, Kerley-Hamilton JS, Teegarden A, Tomlinson CR, Kuintzle R, Simmons N, et al. MicroRNA and gene expression changes in unruptured human cerebral aneurysms. J Neurosurg. 2016;125(6):1390–9.
Nakaoka H, Tajima A, Yoneyama T, Hosomichi K, Kasuya H, Mizutani T, et al. Gene expression profiling reveals distinct molecular signatures associated with the rupture of intracranial aneurysm. Stroke. 2014;45(8):2239–45.
Eden E, Navon R, Steinfeld I, Lipson D, Yakhini Z. GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists. BMC bioinformatics. 2009;10:48.
Tutino VM, Poppenberg KE, Jiang K, Jarvis JN, Sun Y, Sonig A, et al. Circulating neutrophil transcriptome may reveal intracranial aneurysm signature. PLoS One. 2018;13(1):e0191407.
Pera J, Korostynski M, Golda S, Piechota M, Dzbek J, Krzyszkowski T, et al. Gene expression profiling of blood in ruptured intracranial aneurysms: in search of biomarkers. J Cereb Blood Flow Metab. 2013;33(7):1025–31.
Jin H, Li C, Ge H, Jiang Y, Li Y. Circulating microRNA: a novel potential biomarker for early diagnosis of intracranial aneurysm rupture a case control study. J Transl Med. 2013;11:296.
Li P, Zhang Q, Wu X, Yang X, Zhang Y, Li Y, et al. Circulating microRNAs serve as novel biological markers for intracranial aneurysms. J Am Heart Assoc. 2014;3(5):e000972.
Sabatino G, Rigante L, Minella D, Novelli G, Della Pepa GM, Esposito G, et al. Transcriptional profile characterization for the identification of peripheral blood biomarkers in patients with cerebral aneurysms. J Biol Regul Homeost Agents. 2013;27(3):729–38.
Caranci F, Briganti F, Cirillo L, Leonardi M, Muto M. Epidemiology and genetics of intracranial aneurysms. Eur J Radiol. 2013;82(10):1598–605.
Colige A, Sieron AL, Li S-W, Schwarze U, Petty E, Wertelecki W, et al. Human Ehlers-Danlos syndrome type VII C and bovine Dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene. Am J Hum Genet. 1999;65(2):308–17.
Byers Peter H, Duvic M, Atkinson M, Robinow M, Smith Lynne T, Krane Stephen M, et al. Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen. Am J Med Genet. 1998;72(1):94–105.
Ronkainen A, Hernesniemi J, Puranen M, Niemitukia L, Vanninen R, Ryynänen M, et al. Familial intracranial aneurysms. Lancet. 1997;349(9049):380–4.
Abrantes P, Santos MM, Sousa I, Xavier JM, Francisco V, Krug T, et al. Genetic variants underlying risk of intracranial aneurysms: insights from a GWAS in Portugal. PLoS One. 2015;10(7):e0133422.
Bilguvar K, Yasuno K, Niemela M, Ruigrok YM, von Und Zu Fraunberg M, van Duijn CM, et al. Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet. 2008;40(12):1472–7.
Deka R, Koller DL, Lai D, Indugula SR, Sun G, Woo D, et al. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke. 2010;41(6):1132–7.
Foroud T, Koller DL, Lai D, Sauerbeck L, Anderson C, Ko N, et al. Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Stroke. 2012;43(11):2846–52.
Foroud T, Lai D, Koller D, Van't Hof F, Kurki MI, Anderson CS, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke. 2014;45(11):3194–9.
Kurki MI, Gaal EI, Kettunen J, Lappalainen T, Menelaou A, Anttila V, et al. High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms. PLoS Genet. 2014;10(1):e1004134.
Low SK, Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, et al. Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA. Hum Mol Genet. 2012;21(9):2102–10.
Yasuno K, Bakircioglu M, Low SK, Bilguvar K, Gaal E, Ruigrok YM, et al. Common variant near the endothelin receptor type a (EDNRA) gene is associated with intracranial aneurysm risk. Proc Natl Acad Sci U S A. 2011;108(49):19707–12.
Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet. 2010;42(5):420–5.
Helgadottir A, Thorleifsson G, Magnusson KP, Gretarsdottir S, Steinthorsdottir V, Manolescu A, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008;40(2):217–24.
Alg VS, Sofat R, Houlden H, Werring DJ. Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals. Neurology. 2013;80(23):2154–65.
Zhu L, Jiang K, Webber K, Wong L, Liu T, Chen Y, et al. Chromatin landscapes and genetic risk for juvenile idiopathic arthritis. Arthritis Res Ther. 2017;19:57.
Maurano MT, Humbert R, Rynes E, Thurman RE, Haugen E, Wang H, et al. Systematic localization of common disease-associated variation in regulatory DNA. Science. 2012;337(6099):1190–5.
Schaub MA, Boyle AP, Kundaje A, Batzoglou S, Snyder M. Linking disease associations with regulatory information in the human genome. Genome Res. 2012;22(9):1748–59.
Farh KK, Marson A, Zhu J, Kleinewietfeld M, Housley WJ, Beik S, et al. Genetic and epigenetic fine mapping of causal autoimmune disease variants. Nature. 2015;518(7539):337–43.
Martin P, McGovern A, Orozco G, Duffus K, Yarwood A, Schoenfelder S, et al. Capture Hi-C reveals novel candidate genes and complex long-range interactions with related autoimmune risk loci. Nat Commun. 2015;6:10069. https://doi.org/10.1038/ncomms10069.
The Encode Project Consortium, Dunham I, Kundaje A, Aldred SF, Collins PJ, Davis CA, et al. An integrated encyclopedia of DNA elements in the human genome. Nature. 2012;489:57–74.
Yu L, Wang J, Wang S, Zhang D, Zhao Y, Wang R, et al. DNA methylation regulates gene expression in intracranial aneurysms. World Neurosurg. 2017;105(Sep):28–36.
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, de Bakker PIW. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics. 2008;24(24):2938–9.
Zentner GE, Tesar PJ, Scacheri PC. Epigenetic signatures distinguish multiple classes of enhancers with distinct cellular functions. Genet Res. 2011;21(8):1273–83.
Jiang K, Zhu L, Buck MJ, Chen Y, Carrier B, Liu T, et al. Disease-associated SNPs from non-coding regions in juvenile idiopathic arthritis are located within or adjacent to functional genomic elements of human neutrophils and CD4+ T cells. Arthritis Rheumatol. 2015;67(7):1966–77.
Olsson S, Csajbok LZ, Jood K, Nylén K, Nellgård B, Jern C. Association between genetic variation on chromosome 9p21 and aneurysmal subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry. 2011;82(4):384–8.
Quinlan AR, Hall IM. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics. 2010;26(6):841–2.
Chyatte D, Bruno G, Desai S, Todor DR. Inflammation and intracranial aneurysms. Neurosurgery. 1999;45(5):1137–47.
Huang DW, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2008;4(1):44–57.
Huang DW, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res. 2009;37(1):1–13.
Boyle EI, Weng S, Gollub J, Jin H, Botstein D, Cherry JM, et al. GO::TermFinder—open source software for accessing gene ontology information and finding significantly enriched gene ontology terms associated with a list of genes. Bioinformatics (Oxford, England). 2004;20(18):3710–5.
Gautier L, Cope L, Bolstad BM, Irizarry RA. Affy—analysis of Affymetrix GeneChip data at the probe level. Bioinformatics. 2004;20(3):307–15.
Storey JD. A direct approach to false discovery rates. J Royal Stat Soc Ser B (Statistical Methodology). 2002;64(3):479–98.
Carlson M. Genome wide annotation for humanR package version 3.5.0. http://www.bioconductor.org/packages/release/data/annotation/html/org.Hs.eg.db.html; 2017.
Ahituv N. Exonic enhancers: proceed with caution in exome and genome sequencing studies. Genome Med. 2016;8(1):14.
Kim ST, Brinjikji W, Kallmes DF. Prevalence of intracranial aneurysms in patients with connective tissue diseases: a retrospective study. AJNR Am J Neuroradiol. 2016;37(8):1422–6.
Vega C, Kwoon JV, Lavine SD. Intracranial aneurysms: current evidence and clinical practice. Am Fam Physician. 2002;66(4):601–8.
Ong C-T, Corces VG. CTCF: an architectural protein bridging genome topology and function. Nat Rev Genet. 2014;15(4):234–46.
Phillips JE, Corces VG. CTCF: master weaver of the genome. Cell. 2009;137(7):1194–211.
Alexander RP, Fang G, Rozowsky J, Snyder M, Gerstein MB. Annotating non-coding regions of the genome. Nat Rev Genet. 2010;11(8):559–71.
Takemata N, Ohta K. Role of non-coding RNA transcription around gene regulatory elements in transcription factor recruitment. RNA Biol. 2017;14(1):1–5.
Lüscher B. Function and regulation of the transcription factors of the Myc/max/mad network. Gene. 2001;277(1–2):1–14.
Humphrey JD, Taylor CA. Intracranial and abdominal aortic aneurysms: similarities, differences, and need for a new class of computational models. Annu Rev Biomed Eng. 2008;10:221–46.
Jamous MA, Nagahiro S, Kitazato KT, Satoh K, Satomi J. Vascular corrosion casts mirroring early morphological changes that lead to the formation of saccular cerebral aneurysm: an experimental study in rats. J Neurosurg. 2005;102(3):532–5.
Nixon AM, Gunel M, Sumpio BE. The critical role of hemodynamics in the development of cerebral vascular disease. J Neurosurg. 2009;112(6):1240–53.
Meng H, Tutino VM, Xiang J, Siddiqui A. High WSS or low WSS? Complex interactions of hemodynamics with intracranial aneurysm initiation, growth, and rupture: toward a unifying hypothesis. AJNR Am J Neuroradiol. 2014;35(7):1254–62.
Frösen J, Tulamo R, Paetau A, Laaksamo E, Korja M, Laakso A, et al. Saccular intracranial aneurysm: pathology and mechanisms. Acta Neuropathol. 2012;123(6):773–86.
Groselj-Grenc M, Ihan A, Derganc M. Neutrophil and monocyte CD64 and CD163 expression in critically ill neonates and children with sepsis: comparison of fluorescence intensities and calculated indexes. Mediators Inflamm. 2008;2008:202646.
van den Berg JS, Pals G, Arwert F, Hennekam RC, Albrecht KW, Westerveld A, et al. Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation? Stroke. 1999;30(8):1628–31.
Nicholls AC, De Paepe A, Narcisi P, Dalgleish R, De Keyser F, Matton M, et al. Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree. Hum Genet. 1988;78:0340–6717 Print.
Schwarze U, Hata R-I, McKusick VA, Shinkai H, Hoyme HE, Pyeritz RE, et al. Rare autosomal recessive cardiac Valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway. Am J Hum Genet. 2004;74(5):917–30.
Mendoza FA, Piera-Velazquez S, Farber JL, Feghali-Bostwick C, Jimenez SA. Endothelial cells expressing endothelial and mesenchymal cell gene products in systemic sclerosis-associated interstitial lung disease lung tissues. Arthritis Rheumatol. 2016;68(1):210–7.
Ross R. Connective tissue cells, cell proliferation and synthesis of extracellular matrix — a review. Philos Trans R Soc Lond B Biol Sci. 1975;271(912):247–59.
Burke J, Balian G, Ross R, Bornstein P. Synthesis of types I and III procollagen and collagen by monkey aortic smooth muscle cells in vitro. Biochemistry. 1977;16(14):3243–9.
Bruno G, Todor R, Lewis I, Chyatte D. Vascular extracellular matrix remodeling in cerebral aneurysms. J Neurosurg. 1998;89(3):431–40.
Kataoka K, Taneda M, Asai T, Kinoshita A, Ito M, Kuroda R. Structural fragility and inflammatory response of ruptured cerebral aneurysms. A comparative study between ruptured and unruptured cerebral aneurysms. Stroke. 1999;30(7):1396–401.
Kalsheker NA. α1-antichymotrypsin. Int J Biochem Cell Biol. 1996;28(9):961–4.
Wilson TJ, Nannuru KC, Singh RK. Cathepsin G–mediated activation of pro–matrix metalloproteinase 9 at the tumor-bone Interface promotes transforming growth factor-β signaling and bone destruction. Mol Cancer Res. 2009;7(8):1224–33.
Beatty K, Bieth J, Travis J. Kinetics of association of serine proteinases with native and oxidized alpha-1-proteinase inhibitor and alpha-1-antichymotrypsin. J Biol Chem. 1980;255(9):3931–4.
Han Y-P, Yan C, Garner WL. Proteolytic activation of matrix Metalloproteinase-9 in skin wound healing is inhibited by α-1-Antichymotrypsin. J Invest Dermatol. 2008;128(9):2334–42.
Savitz AJ, Meyer DI. 180-kD ribosome receptor is essential for both ribosome binding and protein translocation. J Cell Biol. 1993;120(4):853.
Yanagisawa M, Kurihara H, Kimura S, Tomobe Y, Kobayashi M, Mitsui Y, et al. A novel peptide vasoconstrictor produced by vascular endothelial cells. Nature. 1988;332(6163):411–5.
Zhang YM, Wang K, Zhou G-M, Zuo J, Ge JB. Endothelin-1 promoted proliferation of vascular smooth muscle cell through pathway of extracellular signal-regulated kinase and cyclin D1. Acta Pharmacol Sin. 2003;24(6):563–8.
Boualleque A, Daou GB, Srivastava AK. Endothelin-1-induced signaling pathways in vascular smooth muscle cells. Curr Vasc Pharmacol. 2007;5(1):45–52.
Böhm F, Pernow J. The importance of endothelin-1 for vascular dysfunction in cardiovascular disease. Cardiovasc Res. 2007;76(1):8–18.
Stefansson B, Ohama T, Daugherty AE, Brautigan DL. Protein phosphatase 6 regulatory subunits composed of Ankyrin repeat domains. Biochemistry. 2008;47(5):1442–51.
Aoki T, Kataoka H, Shimamura M, Nakagami H, Wakayama K, Moriwaki T, et al. NF-κB is a key mediator of cerebral aneurysm formation. Circulation. 2007;116(24):2830–40.
Hasan D, Chalouhi N, Jabbour P, Hashimoto T. Macrophage imbalance (M1 vs. M2) and upregulation of mast cells in wall of ruptured human cerebral aneurysms: preliminary results. J Neuroinflammation. 2012;9(1):222.
Hosaka K, Hoh BL. Inflammation and cerebral aneurysms. Transl Stroke Res. 2014;5(2):190–8.
Sablotzki A, Ebel H, Mühling J, Dehne MG, Nopens H, Giesselmann H, et al. Dysregulation of immune response following neurosurgical operations. Acta Anaesthesiol Scand. 2000;44(1):82–7.
Brull DJ, Montgomery HE, Sanders J, Dhamrait S, Luong L, Rumley A, et al. Interleukin-6 gene -174g>c and -572g>c promoter polymorphisms are strong predictors of plasma interleukin-6 levels after coronary artery bypass surgery. Arterioscler Thromb Vasc Biol. 2001;21(9):1458–63.
Peter M, Kyaw Zayar T, Pankaj S. The genetics of sporadic ruptured and unruptured intracranial aneurysms: a genetic meta-analysis of 8 genes and 13 polymorphisms in approximately 20,000 individuals. J Neurosurg. 2010;112(4):714–21.
Sotoodehnejadnematalahi F, Burke B. Structure, function and regulation of versican: the most abundant type of proteoglycan in the extracellular matrix. Acta Med Iran. 2013;51(11):740–50.
Wight TN, Kang I, Merrilees MJ. Versican and the control of inflammation. Matrix Biol. 2014;35:152–61.
Segev A, Nili N, Strauss BH. The role of perlecan in arterial injury and angiogenesis. Cardiovasc Res. 2004;63(4):603–10.
Laarman MD, Vermunt MW, Kleinloog R, de Boer-Bergsma JJ, Brain Bank N, Rinkel GJE, et al. Intracranial aneurysm-associated single-nucleotide polymorphisms Alter regulatory DNA in the human circle of Willis. Stroke. 2018;49(2):447–53.
Laarman MD, Geeven G, Barnett P, Rinkel GJE, de Laat W, Ruigrok YM, et al. Chromatin conformation links putative enhancers in intracranial aneurysm-associated regions to potential candidate genes. J Am Heart Assoc. 2019;8(9):e011201.
Cheung AK, Faezi-Jenkin B, Leypoldt JK. Effect of thrombosis on complement activation and neutrophil degranulation during in vitro hemodialysis. J Am Soc Nephrol. 1994;5(1):110–5.
Kim KH, Barazia A, Cho J. Real-time imaging of heterotypic platelet-neutrophil interactions on the activated endothelium during vascular inflammation and thrombus formation in live mice. J Vis Exp. 2013;74(Apr):50329. https://doi.org/10.3791/50329.
Soehnlein O. Multiple roles for neutrophils in atherosclerosis. Circ Res. 2012;110(6):875–88.
Chu Y, Wilson K, Gu H, Wegman-Points L, Dooley SA, Pierce GL, et al. Myeloperoxidase is increased in human cerebral aneurysms and increases formation and rupture of cerebral aneurysms in mice. Stroke. 2015;46(6):1651–6.
Tutino VM, Poppenberg KE, Li L, Shallwani H, Jiang K, Jarvis JN, et al. Biomarkers from circulating neutrophil transcriptomes have potential to detect unruptured intracranial aneurysms. J Transl Med. 2018;16(1):373.
Chi J-T, Chang HY, Haraldsen G, Jahnsen FL, Troyanskaya OG, Chang DS, et al. Endothelial cell diversity revealed by global expression profiling. Proc Natl Acad Sci U S A. 2003;100(19):10623–8.
Kessler H, Jiang K, Jarvis JN. Using chromatin architecture to understand the genetics and transcriptomics of juvenile idiopathic arthritis. Front Immunol. 2018;9(eCollection):2964.
We thank Paul H. Dressel BFA for preparation of the illustrations and W. Fawn Dorr BA and Debra J. Zimmer for editorial assistance.
This research was supported by the Brain Aneurysm Foundation, by the Carol W. Harvey Chair of Research (VMT and HM), Dawn Brejcha Chair of Research (VMT), Robert Southerland Chair of Research (VMT), Kristen’s Legacy of Love for Kristen Shafer Englert Chair of Research (HM), TeamCindy – Alcatraz Chair of Research (HM) grants. The Brain Aneurysm Foundation was not involved in the study design, the collection, analysis and interpretation of data, or the writing of the manuscript.
Ethics approval and consent to participate
Consent for publication
KEP: none; KJ: none; MKT: none; KVS: Consulting and teaching for Canon Medical Systems Corporation, Penumbra Inc., Medtronic, and Jacobs Institute. Founder: Neurovascular Diagnostics, Inc.; AHS: Financial Interest/Investor/Stock Options/Ownership: Amnis Therapeutics, Apama Medical, BlinkTBI, Inc., Buffalo Technology Partners, Inc., Cardinal Health, Cerebrotech Medical Systems, Inc., Claret Medical, Cognition Medical, Endostream Medical, Ltd., Imperative Care, International Medical Distribution Partners, Rebound Therapeutics Corp., Silk Road Medical, StimMed, Synchron, Three Rivers Medical, Inc., Viseon Spine, Inc. Consultant/Advisory Board: Amnis Therapeutics, Boston Scientific, Canon Medical Systems USA, Inc., Cerebrotech Medical Systems, Inc., Cerenovus, Claret Medical, Corindus, Inc., Endostream Medical, Ltd., Guidepoint Global Consulting, Imperative Care, Integra, Medtronic, MicroVention, Northwest University – DSMB Chair for HEAT Trial, Penumbra, Rapid Medical, Rebound Therapeutics Corp., Silk Road Medical, StimMed, Stryker, Three Rivers Medical, Inc., VasSol, W.L. Gore & Associates. National PI/Steering Committees: Cerenovus NAPA Trial and ARISE II Trial, Medtronic SWIFT PRIME and SWIFT DIRECT Trials, MicroVention FRED Trial & CONFIDENCE Study, MUSC POSITIVE Trial, Penumbra 3D Separator Trial, COMPASS Trial, INVEST Trial; JK: none; JNJ: none; HM: Founder Neurovascular Diagnostics, Inc.; VMT: Founder Neurovascular Diagnostics, Inc.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1: Table S1. Entire list of significant ontologies from GO::TermFinder. Fig. S1. Gene Ontology term finder molecular process results for genes within extended intracranial aneurysm-associated linkage disequilibrium blocks. Blocks in blue represent significant ontologies. Fig S2. Gene Ontology term finder molecular component results for genes within extended intracranial aneurysm-associated linkage disequilibrium blocks. Blocks in blue represent significant ontologies.
About this article
Cite this article
Poppenberg, K.E., Jiang, K., Tso, M.K. et al. Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium. BMC Med Genomics 12, 149 (2019) doi:10.1186/s12920-019-0591-7
- Cell type
- Cerebral aneurysm