Reduction of neuronal activity mediated by blood-vessel regression in the brain

Author:

Gao Xiaofei,Li Jun-Liszt,Chen Xingjun,Ci Bo,Chen Fei,Lu Nannan,Shen Bo,Zheng Lijun,Jia Jie-Min,Yi Yating,Zhang Shiwen,Shi Ying-Chao,Shi Kaibin,Propson Nicholas E,Huang Yubin,Poinsatte Katherine,Zhang Zhaohuan,Yue Yuanlei,Bosco Dale B,Lu Ying-mei,Yang Shi-bing,Adams Ralf H.,Lindner Volkhard,Huang Fen,Wu Long-Jun,Zheng Hui,Han Feng,Hippenmeyer Simon,Stowe Ann M.,Peng Bo,Margeta Marta,Wang Xiaoqun,Liu Qiang,Körbelin Jakob,Trepel Martin,Lu Hui,Zhou Bo O.,Zhao Hu,Su Wenzhi,Bachoo Robert M.,Ge Woo-pingORCID

Abstract

SummaryThe brain vasculature supplies neurons with glucose and oxygen, but little is known about how vascular plasticity contributes to brain function. Using longitudinal in vivo imaging, we reported that a substantial proportion of blood vessels in the adult brain sporadically occluded and regressed. Their regression proceeded through sequential stages of blood-flow occlusion, endothelial cell collapse, relocation or loss of pericytes, and retraction of glial endfeet. Regressing vessels were found to be widespread in mouse, monkey and human brains. Both brief occlusions of the middle cerebral artery and lipopolysaccharide-mediated inflammation induced an increase of vessel regression. Blockage of leukocyte adhesion to endothelial cells alleviated LPS-induced vessel regression. We further revealed that blood vessel regression caused a reduction of neuronal activity due to a dysfunction in mitochondrial metabolism and glutamate production. Our results elucidate the mechanism of vessel regression and its role in neuronal function in the adult brain.

Publisher

Cold Spring Harbor Laboratory

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