Morganti Claudia, Cabezas-Wallscheid Nina, Ito Keisuke
Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, NY, USA.
Departments of Cell Biology and Stem Cell Institute, Albert Einstein College of Medicine, Bronx, NY, USA.
Hemasphere. 2022 Jun 28;6(7):e740. doi: 10.1097/HS9.0000000000000740. eCollection 2022 Jul.
Cellular metabolism is a key regulator of hematopoietic stem cell (HSC) maintenance. HSCs rely on anaerobic glycolysis for energy production to minimize the production of reactive oxygen species and shift toward mitochondrial oxidative phosphorylation upon differentiation. However, increasing evidence has shown that HSCs still maintain a certain level of mitochondrial activity in quiescence, and exhibit high mitochondrial membrane potential, which both support proper HSC function. Since glycolysis and the tricarboxylic acid (TCA) cycle are not directly connected in HSCs, other nutrient pathways, such as amino acid and fatty acid metabolism, generate acetyl-CoA and provide it to the TCA cycle. In this review, we discuss recent insights into the regulatory roles of cellular metabolism in HSCs. Understanding the metabolic requirements of healthy HSCs is of critical importance to the development of new therapies for hematological disorders.
细胞代谢是造血干细胞(HSC)维持的关键调节因子。造血干细胞依靠无氧糖酵解产生能量,以尽量减少活性氧的产生,并在分化时转向线粒体氧化磷酸化。然而,越来越多的证据表明,造血干细胞在静止状态下仍保持一定水平的线粒体活性,并表现出高线粒体膜电位,这两者都支持造血干细胞的正常功能。由于糖酵解和三羧酸(TCA)循环在造血干细胞中不直接相连,其他营养途径,如氨基酸和脂肪酸代谢,会产生乙酰辅酶A并将其提供给TCA循环。在这篇综述中,我们讨论了细胞代谢在造血干细胞中的调节作用的最新见解。了解健康造血干细胞的代谢需求对于开发血液系统疾病的新疗法至关重要。