| Literature DB >> 31761722 |
Jun Wang1, Yaxiong Cui1, Zhenyang Yu1, Wenjing Wang2, Xuan Cheng1, Wenliang Ji3, Shuyue Guo3, Qing Zhou2, Ning Wu4, Yan Chen2, Ying Chen4, Xiaopeng Song1, Hui Jiang2, Yanxiao Wang1, Yu Lan1, Bin Zhou5, Lanqun Mao3, Jin Li4, Huanming Yang6, Weixiang Guo7, Xiao Yang8.
Abstract
Increased understanding of the functions of lactate has suggested a close relationship between lactate homeostasis and normal brain activity because of its importance as an energy source and signaling molecule. Here we show that lactate levels affect adult hippocampal neurogenesis. Cerebrovascular-specific deletion of PTEN causes learning and memory deficits and disrupts adult neurogenesis with accompanying lactate accumulation. Consistently, administering lactate to wild-type animals impairs adult hippocampal neurogenesis. The endothelial PTEN/Akt pathway increases monocarboxylic acid transporter 1 (MCT1) expression to enhance lactate transport across the brain endothelium. Moreover, cerebrovascular overexpression of MCT1 or deletion of Akt1 restores MCT1 expression, decreases lactate levels, and normalizes hippocampal neurogenesis and cognitive function in PTEN mutant mice. Together, these findings delineate how the brain endothelium maintains lactate homeostasis and contributes to adult hippocampal neurogenesis and cognitive functions.Entities:
Keywords: CRISPR-Cas9; PTEN/Akt signaling; adult neurogenesis; cerebrovascular endothelial cell; cognition; lactate; monocarboxylic acid transporter 1
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Year: 2019 PMID: 31761722 DOI: 10.1016/j.stem.2019.09.009
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633