Song Zhangfa, Ju Zhenyu, Rudolph K Lenhard
Institute of Molecular Medicine and Max-Planck-Research Group on Stem Cell Aging, University of Ulm, 89081 Ulm, Germany.
Exp Gerontol. 2009 Jan-Feb;44(1-2):75-82. doi: 10.1016/j.exger.2008.06.009. Epub 2008 Jul 3.
The function of adult stem cells declines during aging and chronic diseases. An understanding of the molecular mechanisms underlying these processes will help to identify targets for future therapies in order to improve regenerative reserve and organ maintenance. Telomere shortening represents a cell intrinsic mechanism inducing DNA damage in aging cells. Current studies in telomerase knockout mice have shown that telomere dysfunction induces cell intrinsic checkpoints and environmental alteration that limit stem cell function. While these phenotypes differ from wild-type mice with long telomere reserves, they appear to be relevant for human aging, which is associated with an accumulation of telomere dysfunction and DNA damage.
成体干细胞的功能在衰老和慢性疾病过程中会下降。了解这些过程背后的分子机制将有助于确定未来治疗的靶点,以改善再生储备和器官维持。端粒缩短是一种诱导衰老细胞中DNA损伤的细胞内在机制。目前对端粒酶敲除小鼠的研究表明,端粒功能障碍会诱导细胞内在检查点和环境改变,从而限制干细胞功能。虽然这些表型与具有长端粒储备的野生型小鼠不同,但它们似乎与人类衰老相关,而人类衰老与端粒功能障碍和DNA损伤的积累有关。