Mitochondrial Mechanisms of Metabolic Reprogramming in Proliferating Cells

被引:1
作者
Sousa, Maria Ines [1 ,2 ]
Rodrigues, Ana Sofia [1 ,2 ]
Pereira, Sandro [1 ]
Perestrelo, Tania [1 ,2 ,3 ]
Correia, Marcelo [1 ,2 ,3 ]
Ramalho-Santos, Joao [1 ,4 ]
机构
[1] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Biol Reprod & Stem Cell Grp, P-3001401 Coimbra, Portugal
[2] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Programme Expt Biol & Biomed, P-3001401 Coimbra, Portugal
[3] Univ Coimbra, IIIUC Inst Interdisciplinary Res, P-3001401 Coimbra, Portugal
[4] Univ Coimbra, Dept Life Sci, P-3001401 Coimbra, Portugal
关键词
Glycolysis; metabolism; nuclear reprogramming; oxidative phosphorylation; pluripotency; regenerative medicine; PLURIPOTENT STEM-CELLS; HUMAN SOMATIC-CELLS; ENERGY-METABOLISM; HUMAN FIBROBLASTS; CANCER; MOUSE; INDUCTION; GENERATION; DIFFERENTIATION; METHYLATION;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are responsible for coordinating cellular energy production in the vast majority of somatic cells, and every cell type in a specific state can have a distinct metabolic signature. The metabolic requirements of cells from different tissues changes as they proliferate/differentiate, and cellular metabolism must match these demands. Proliferating cells, namely cancer cells and stem cells, tend to prefer glycolysis rather than a more oxidative metabolism. This preference has been exploited for the improvement of new biotechnological and therapeutic applications. In this review, we describe mitochondrial dynamics and energy metabolism modulation during nuclear reprogramming of somatic cells, which will be essential for the development and optimization of new protocols for regenerative medicine, disease modeling and toxicological screens involving patient-specific reprogrammed cells.
引用
收藏
页码:2493 / 2504
页数:12
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