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Fibrinogen in mice cerebral microvessels induces blood-brain barrier dysregulation with aging via a dynamin-related protein 1-dependent pathway.小鼠脑微血管中的纤维蛋白原通过一种与动力蛋白相关蛋白 1 相关的途径诱导血脑屏障随年龄增长而失调。
Geroscience. 2024 Feb;46(1):395-415. doi: 10.1007/s11357-023-00988-y. Epub 2023 Oct 28.
2
Diffusion prepared pseudo-continuous arterial spin labeling reveals blood-brain barrier dysfunction in patients with CADASIL.磁共振弥散加权伪连续动脉自旋标记技术显示 CADASIL 患者血脑屏障功能障碍。
Eur Radiol. 2023 Oct;33(10):6959-6969. doi: 10.1007/s00330-023-09652-7. Epub 2023 Apr 26.
3
Endothelial depletion of Atg7 triggers astrocyte-microvascular disassociation at blood-brain barrier.Atg7 敲除导致血脑屏障内皮细胞耗竭及星形胶质细胞-微血管分离。
J Cell Biol. 2023 May 1;222(5). doi: 10.1083/jcb.202103098. Epub 2023 Mar 30.
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Current state and guidance on arterial spin labeling perfusion MRI in clinical neuroimaging.目前在临床神经影像学中动脉自旋标记灌注 MRI 的现状和指导建议。
Magn Reson Med. 2023 May;89(5):2024-2047. doi: 10.1002/mrm.29572. Epub 2023 Jan 25.
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Blood-brain barrier dysfunction promotes astrocyte senescence through albumin-induced TGFβ signaling activation.血脑屏障功能障碍通过白蛋白诱导的 TGFβ 信号激活促进星形胶质细胞衰老。
Aging Cell. 2023 Feb;22(2):e13747. doi: 10.1111/acel.13747. Epub 2023 Jan 5.
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Aging Dis. 2022 Oct 1;13(5):1546-1561. doi: 10.14336/AD.2022.0225.

衰老过程中血脑屏障的改变。

Alterations of the blood-brain barrier during aging.

作者信息

Cao Yufan, Xu Weihai, Liu Qing

机构信息

Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

J Cereb Blood Flow Metab. 2024 Jun;44(6):881-895. doi: 10.1177/0271678X241240843. Epub 2024 Mar 21.

DOI:10.1177/0271678X241240843
PMID:38513138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11318406/
Abstract

The blood-brain barrier (BBB) is a complex and dynamic interface that regulates the exchange of molecules and cells between the blood and the central nervous system. It undergoes structural and functional changes during aging, which may compromise its integrity and contribute to the pathogenesis of neurodegenerative diseases. In recent years, advances in microscopy and high-throughput bioinformatics have allowed a more in-depth investigation of the aging mechanisms of BBB. This review summarizes age-related alterations of the BBB structure and function from six perspectives: endothelial cells, astrocytes, pericytes, basement membrane, microglia and perivascular macrophages, and fibroblasts, ranging from the molecular level to the human multi-system level. These basic components are essential for the proper functioning of the BBB. Recent imaging methods of BBB were also reviewed. Elucidation of age-associated BBB changes may offer insights into BBB homeostasis and may provide effective therapeutic strategies to protect it during aging.

摘要

血脑屏障(BBB)是一个复杂且动态的界面,它调节着血液与中枢神经系统之间分子和细胞的交换。在衰老过程中,它会发生结构和功能上的变化,这可能会损害其完整性,并导致神经退行性疾病的发病机制。近年来,显微镜技术和高通量生物信息学的进展使得对血脑屏障衰老机制的研究更加深入。本综述从六个方面总结了血脑屏障结构和功能与年龄相关的变化:内皮细胞、星形胶质细胞、周细胞、基底膜、小胶质细胞和血管周围巨噬细胞以及成纤维细胞,范围从分子水平到人类多系统水平。这些基本组成部分对于血脑屏障的正常功能至关重要。还综述了血脑屏障的最新成像方法。阐明与年龄相关的血脑屏障变化可能有助于深入了解血脑屏障的稳态,并可能为在衰老过程中保护血脑屏障提供有效的治疗策略。