Calico Life Sciences, South San Francisco, CA
Robin Chemers Neustein Laboratory of Mammalian Cell Biology and Development, Howard Hughes Medical Institute, The Rockefeller University, New York, NY
J Cell Biol. 2018 Jan 2;217(1):79-92. doi: 10.1083/jcb.201708099. Epub 2017 Oct 25.
Stem cells are imbued with unique qualities. They have the capacity to propagate themselves through symmetric divisions and to divide asymmetrically to engender new cells that can progress to differentiate into tissue-specific, terminal cell types. Armed with these qualities, stem cells in adult tissues are tasked with replacing decaying cells and regenerating tissue after injury to maintain optimal tissue function. With increasing age, stem cell functional abilities decline, resulting in reduced organ function and delays in tissue repair. Here, we review the effect of aging in five well-studied adult murine stem cell populations and explore age-related declines in stem cell function and their consequences for stem cell self-renewal, tissue homeostasis, and regeneration. Finally, we examine transcriptional changes that have been documented in aged stem cell populations and discuss new questions and future directions that this collection of data has uncovered.
干细胞具有独特的性质。它们能够通过对称分裂自我繁殖,并通过不对称分裂产生新的细胞,这些新的细胞可以进一步分化为组织特异性的终末细胞类型。凭借这些特性,成年组织中的干细胞负责在受伤后替换衰老的细胞并再生组织,以维持最佳的组织功能。随着年龄的增长,干细胞的功能能力下降,导致器官功能降低和组织修复延迟。在这里,我们综述了在五个研究充分的成年鼠干细胞群体中衰老的影响,并探讨了与年龄相关的干细胞功能下降及其对干细胞自我更新、组织稳态和再生的影响。最后,我们检查了在衰老的干细胞群体中记录的转录变化,并讨论了这组数据揭示的新问题和未来方向。