Age-Associated mRNA and miRNA Expression Changes in the Blood-Brain Barrier

被引:21
|
作者
Goodall, Emily F. [1 ]
Leach, Vicki [1 ]
Wang, Chunfang [2 ]
Cooper-Knock, Johnathan [1 ]
Heath, Paul R. [1 ]
Baker, David [1 ]
Drew, David R. [1 ]
Saffrey, M. Jill [2 ]
Simpson, Julie E. [1 ]
Romero, Ignacio A. [2 ]
Wharton, Stephen B. [1 ]
机构
[1] Univ Sheffield, Sheffield Inst Translat Neurosci, 385a Glossop Rd, Sheffield S10 2HQ, S Yorkshire, England
[2] Open Univ, Fac Sci Technol Engn & Math, Sch Life Sci Hlth & Chem Sci, Walton Hall, Milton Keynes MK7 6AA, Bucks, England
基金
英国生物技术与生命科学研究理事会;
关键词
ageing; blood brain barrier; gene expression; miRNA; DNA-DAMAGE RESPONSE; GENE-EXPRESSION; ALZHEIMERS-DISEASE; GLIOBLASTOMA VESSELS; ENDOTHELIAL-CELLS; CEREBRAL-CORTEX; UP-REGULATION; MICRORNA; PERMEABILITY; MICROARRAY;
D O I
10.3390/ijms20123097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Functional and structural age-associated changes in the blood-brain barrier (BBB) may affect the neurovascular unit and contribute to the onset and progression of age-associated neurodegenerative pathologies, including Alzheimer's disease. The current study interrogated the RNA profile of the BBB in an ageing human autopsy brain cohort and an ageing mouse model using combined laser capture microdissection and expression profiling. Only 12 overlapping genes were altered in the same direction in the BBB of both ageing human and mouse cohorts. These included genes with roles in regulating vascular tone, tight junction protein expression and cell adhesion, all processes prone to dysregulation with advancing age. Integrated mRNA and miRNA network and pathway enrichment analysis of the datasets identified 15 overlapping miRNAs that showed altered expression. In addition to targeting genes related to DNA binding and/or autophagy, many of the miRNAs identified play a role in age-relevant processes, including BBB dysfunction and regulating the neuroinflammatory response. Future studies have the potential to develop targeted therapeutic approaches against these candidates to prevent vascular dysfunction in the ageing brain.
引用
收藏
页数:20
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