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代谢性乳酸生成协调发育中小鼠新皮层的血管生成和祖细胞行为。

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

作者信息

Dong Xiaoxiang, Zhang Qiangqiang, Yu Xiangyu, Wang Ding, Ma Jiaming, Ma Jian, Shi Song-Hai

机构信息

The IDG/McGovern Institute for Brain Research, Tsinghua-Peking Center for Life Sciences, Beijing Frontier Research Centre for Biological Structure, Beijing Advanced Innovation Centre for Structural Biology, School of Life Sciences, Tsinghua University, Beijing, China.

Department of Biological Sciences, Dartmouth College, Hanover, NH, USA.

出版信息

Nat Neurosci. 2022 Jul;25(7):865-875. doi: 10.1038/s41593-022-01093-7. Epub 2022 Jun 20.

DOI:10.1038/s41593-022-01093-7
PMID:35726058
Abstract

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.

摘要

神经祖细胞的正常行为与有序的血管形成相结合,是新皮质发育的基础。然而,协调神经祖细胞行为和血管生长的机制在很大程度上仍然难以捉摸。在这里,我们表明,放射状胶质祖细胞(RGP)强大的乳酸代谢产生共同调节发育中的小鼠新皮质中的血管发育和RGP分裂行为。RGP经历高度有组织的谱系进展程序以产生多种神经后代。系统的单细胞代谢状态分析表明,RGP及其后代表现出与特定细胞类型和谱系进展状态相关的独特代谢特征。对称分裂的增殖性RGP优先表达一组支持葡萄糖摄取和无氧糖酵解的基因。因此,它们在无氧代谢中消耗葡萄糖并产生高水平的乳酸,从而促进血管生长。此外,乳酸产生通过维持线粒体长度来增强RGP增殖。总之,这些结果表明,特定的代谢状态和代谢物在新皮质发育中协调调节血管形成和祖细胞行为。

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