The Key Laboratory of Pathobiology, Ministry of Education, College of Basic Medical Sciences, Jilin University, Changchun, 130021, China.
Stem Cell Rev Rep. 2022 Jun;18(5):1728-1742. doi: 10.1007/s12015-022-10348-6. Epub 2022 Mar 8.
Stem cell senescence and exhaustion are closely related to organ failure and individual aging, which not only induces age-related diseases, but also hinders stem cell applications in regenerative medicine. Thus, it's imminent to find effective ways to delay and retrieve stem cell senescence. Metabolic abnormalities are one of the main characteristics of age-associated declines in stem cell function. Understanding the underlying mechanisms may reveal potential strategies for ameliorating age-associated phenotypes and treating age-related diseases. This review focuses on recent advances in the association between metabolism including glucose, lipid, glutamine and NAD metabolism and stem cell senescence, as well as the other properties like proliferation and differentiation. Layers of studies are summarized to demonstrate how metabolism varies in senescent stem cells and how metabolic reprogramming regulates stem cell senescence. Additionally, we mentioned some recent progress in therapeutic strategies to rejuvenate dysfunctional aged stem cells. Finally, a brief conclusion about the prospect of metabolic regulation as a potential strategy for rescuing stem cell senescence is displayed. Stem cell senescence is induced by the metabolic reprogramming. The metabolic alterations of glucose, lipid, glutamine and NAD can conversely facilitate or inhibit stem cell senescence. Glycolysis, OXPHOS and PPP are all attenuated. But gluconeogenesis alterations still remain unclear. In lipid metabolisms, both FAO and DNL are suppressed. As for the glutamine metabolism, stem cells' dependence on glutamine is enhanced. Last, NAD metabolism undergoes a down-regulated synthesis and up-regulated consumption. All these alterations can be potential targets for reversing stem cell senescence.
干细胞衰老和衰竭与器官衰竭和个体衰老密切相关,不仅会引发与年龄相关的疾病,还会阻碍干细胞在再生医学中的应用。因此,寻找有效的方法来延缓和恢复干细胞衰老迫在眉睫。代谢异常是与干细胞功能相关的年龄下降的主要特征之一。了解其潜在机制可能揭示改善与年龄相关表型和治疗与年龄相关疾病的潜在策略。本综述重点介绍了代谢(包括葡萄糖、脂质、谷氨酰胺和 NAD 代谢)与干细胞衰老之间的关联,以及增殖和分化等其他特性的最新进展。总结了多层研究,以证明衰老干细胞中代谢的变化方式,以及代谢重编程如何调节干细胞衰老。此外,我们还提到了一些最近在治疗策略方面的进展,以恢复功能失调的衰老干细胞。最后,简要总结了代谢调节作为挽救干细胞衰老的潜在策略的前景。代谢重编程诱导干细胞衰老。葡萄糖、脂质、谷氨酰胺和 NAD 的代谢改变可以促进或抑制干细胞衰老。糖酵解、OXPHOS 和 PPP 均减弱。但糖异生改变仍不清楚。在脂质代谢中,脂肪酸氧化 (FAO) 和从头合成 (DNL) 均受到抑制。至于谷氨酰胺代谢,干细胞对谷氨酰胺的依赖性增强。最后,NAD 代谢的合成下调和消耗上调。所有这些改变都可能成为逆转干细胞衰老的潜在靶点。