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衰老导致的血脑屏障功能障碍是由脑内皮细胞衰老引起的。

Blood-brain barrier dysfunction in aging is mediated by brain endothelial senescence.

机构信息

CNC-UC Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.

University of Coimbra, Institute for Interdisciplinary Research, Doctoral Programme in Experimental Biology and Biomedicine (PDBEB), Coimbra, Portugal.

出版信息

Aging Cell. 2024 Sep;23(9):e14270. doi: 10.1111/acel.14270. Epub 2024 Aug 15.

DOI:10.1111/acel.14270
PMID:39143890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11488312/
Abstract

BBB dysfunction during aging is characterized by an increase in its permeability and phenotypic alterations of brain endothelial cells (BECs) including dysregulation of tight junction's expression. Here we have investigated the role of BEC senescence in the dysfunction of the BBB. Our results suggest that the transition from young to aged BBB is mediated, at least in part by BEC senescence.

摘要

随着年龄的增长,BBB 的功能障碍表现为通透性增加和脑内皮细胞(BEC)表型改变,包括紧密连接表达失调。在此,我们研究了 BEC 衰老在 BBB 功能障碍中的作用。我们的结果表明,从年轻 BBB 向衰老 BBB 的转变至少部分是由 BEC 衰老介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/332b/11488312/d3d61a060d82/ACEL-23-e14270-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/332b/11488312/f1531deef5a3/ACEL-23-e14270-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/332b/11488312/d3d61a060d82/ACEL-23-e14270-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/332b/11488312/f1531deef5a3/ACEL-23-e14270-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/332b/11488312/d3d61a060d82/ACEL-23-e14270-g001.jpg

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本文引用的文献

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2
Pharmacologically reversible zonation-dependent endothelial cell transcriptomic changes with neurodegenerative disease associations in the aged brain.与神经退行性疾病相关的衰老大脑中,具有药物可逆性的区域依赖性内皮细胞转录组变化。
Nat Commun. 2020 Sep 4;11(1):4413. doi: 10.1038/s41467-020-18249-3.
3
Neuronal regulation of the blood-brain barrier and neurovascular coupling.
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Physiological blood-brain transport is impaired with age by a shift in transcytosis.随着年龄增长,经细胞转运的改变会损害生理性血脑转运。
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