Metabolic lactate production coordinates vasculature development and progenitor behavior in the developing mouse neocortex

被引:39
作者
Dong, Xiaoxiang [1 ]
Zhang, Qiangqiang [1 ]
Yu, Xiangyu [1 ]
Wang, Ding [1 ]
Ma, Jiaming [1 ,2 ]
Ma, Jian [1 ]
Shi, Song-Hai [1 ,3 ]
机构
[1] Tsinghua Univ, IDG McGovern Inst Brain Res, Tsinghua Peking Ctr Life Sci,Sch Life Sci, Beijing Frontier Res Ctr Biol Struct,Beijing Adv, Beijing, Peoples R China
[2] Dartmouth Coll, Dept Biol Sci, Hanover, NH 03755 USA
[3] Chinese Inst Brain Res, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
RADIAL GLIAL-CELLS; NEURAL STEM; SINGLE-CELL; MITOCHONDRIAL DYNAMICS; ASYMMETRIC DIVISION; GENE-EXPRESSION; NEURONS; REQUIREMENTS; REVEALS; PROLIFERATION;
D O I
10.1038/s41593-022-01093-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dong et al. show that proliferative neural progenitors in the developing neocortex preferentially undergo anaerobic glycolysis and generate a high level of lactate that coordinately regulates vasculature outgrowth and progenitor behavior. Proper neural progenitor behavior in conjunction with orderly vasculature formation is fundamental to the development of the neocortex. However, the mechanisms coordinating neural progenitor behavior and vessel growth remain largely elusive. Here we show that robust metabolic production of lactate by radial glial progenitors (RGPs) co-regulates vascular development and RGP division behavior in the developing mouse neocortex. RGPs undergo a highly organized lineage progression program to produce diverse neural progeny. Systematic single-cell metabolic state analysis revealed that RGPs and their progeny exhibit distinct metabolic features associated with specific cell types and lineage progression statuses. Symmetrically dividing, proliferative RGPs preferentially express a cohort of genes that support glucose uptake and anaerobic glycolysis. Consequently, they consume glucose in anaerobic metabolism and produce a high level of lactate, which promotes vessel growth. Moreover, lactate production enhances RGP proliferation by maintaining mitochondrial length. Together, these results suggest that specific metabolic states and metabolites coordinately regulate vasculature formation and progenitor behavior in neocortical development.
引用
收藏
页码:865 / +
页数:32
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