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Series GSE218648 Query DataSets for GSE218648
Status Public on Sep 20, 2023
Title Age-associated changes in murine endothelial gene expression and chromatin accessibility correlate with impaired blood-brain barrier integrity and elevated risk of intracerebral hemorrhage [RRBS]
Organism Mus musculus
Experiment type Methylation profiling by high throughput sequencing
Summary Intracerebral hemorrhage (ICH), a devastating form of stroke, is a leading global cause of human death and disability. The major risk factors for ICH include increasing age, hypertension and cerebral amyloid angiopathy. Despite high mortality and morbidity associated with ICH, the mechanisms leading to blood-brain barrier (BBB) dysfunction with age and development of hemorrhagic stroke is poorly understood. In the vasculature of the central nervous system, endothelial cells (ECs) constitute the core component of the BBB and provide a physical barrier due to tight junctions, adherens junctions, and basement membrane layers. In this study, we show in brains of mice that incidents of intracerebral bleeding increase with advancing age. After isolation of an enriched population of cerebral ECs, we studied gene expression in ECs isolated from murine brains of increasing ages of 2, 6, 12, 18, and 24 months. The study reveals age-dependent dysregulation of 1388 genes in the ECs, including many involved in the maintenance of BBB and vascular integrity. Since epigenetic mechanisms regulate gene expression, we also investigated age-dependent changes at the levels of CpG methylation and accessible chromatin in cerebral ECs. Our study reveals correlations between age-dependent changes in chromatin structure and gene expression. We find significant age-dependent downregulation of the apelin receptor (Aplnr) gene along with an age-dependent reduction in chromatin accessibility of the promoter of this gene. Aplnr is known to play a crucial role in positive regulation of vasodilation and is implicated in vascular health. Interestingly, we also observe an age-dependent reduction in the protein expression levels of the apelin receptor in the brain, potentially implicating the apelin receptor to be critical for the increased risk of intracerebral hemorrhage with ageing.
 
Overall design Reduced Representation Bisulfite Sequencing.
 
Contributor(s) Mohan K, Gasparoni G, Salhab A, Orlich M, Geffers R, Hoffmann S, Adams RH, Walter J, Nordheim A
Citation(s) 37609982
Submission date Nov 23, 2022
Last update date Sep 21, 2023
Contact name Gilles Gasparoni
E-mail(s) gillesgasparoni@gmail.com
Phone +496813022881
Organization name Saarland University
Department Genetics Department
Lab Genetics/Epigenetics
Street address Campus
City Saarbruecken
State/province Saarland
ZIP/Postal code 66123
Country Germany
 
Platforms (1)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
Samples (29)
GSM6754083 12a9_1614 (12 months, female)
GSM6754084 12c2_1617 (12 months, male)
GSM6754085 12d1_1618 (12 months, male)
This SubSeries is part of SuperSeries:
GSE218649 Age-associated changes in murine endothelial gene expression and chromatin accessibility correlate with impaired blood-brain barrier integrity and elevated risk of intracerebral hemorrhage
Relations
BioProject PRJNA904757

Download family Format
SOFT formatted family file(s) SOFTHelp
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE218648_RAW.tar 1.5 Gb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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