Mitochondrial pyruvate metabolism regulates the activation of quiescent adult neural stem cells

被引:44
作者
Petrelli, Francesco [1 ,2 ]
Scandella, Valentina [1 ]
Montessuit, Sylvie [2 ]
Zamboni, Nicola [3 ]
Martinou, Jean-Claude [2 ]
Knobloch, Marlen [1 ]
机构
[1] Univ Lausanne, Dept Biomed Sci, Lausanne, Switzerland
[2] Univ Geneva, Dept Cell Biol, Geneva, Switzerland
[3] Swiss Fed Inst Technol, Inst Mol Syst Biol, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
ELECTRON-TRANSPORT CHAIN; CARRIER; PROLIFERATION; NEUROGENESIS; GLYCOLYSIS; EXPRESSION; DYNAMICS; REVEALS; NESTIN; CANCER;
D O I
10.1126/sciadv.add5220
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cellular metabolism is important for adult neural stem/progenitor cell (NSPC) behavior. However, its role in the transition from quiescence to proliferation is not fully understood. We here show that the mitochondrial pyru-vate carrier (MPC) plays a crucial and unexpected part in this process. MPC transports pyruvate into mitochon-dria, linking cytosolic glycolysis to mitochondrial tricarboxylic acid cycle and oxidative phosphorylation. Despite its metabolic key function, the role of MPC in NSPCs has not been addressed. We show that quiescent NSPCs have an active mitochondrial metabolism and express high levels of MPC. Pharmacological MPC inhibition in-creases aspartate and triggers NSPC activation. Furthermore, genetic Mpc1 ablation in vitro and in vivo also activates NSPCs, which differentiate into mature neurons, leading to overall increased hippocampal neurogen-esis in adult and aged mice. These findings highlight the importance of metabolism for NSPC regulation and identify an important pathway through which mitochondrial pyruvate import controls NSPC quiescence and activation.
引用
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页数:16
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