Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.
Nature. 2012 May 23;485(7400):605-10. doi: 10.1038/nature11061.
Adult stem cells support tissue homeostasis and repair throughout the life of an individual. During ageing, numerous intrinsic and extrinsic changes occur that result in altered stem-cell behaviour and reduced tissue maintenance and regeneration. In the Drosophila testis, ageing results in a marked decrease in the self-renewal factor Unpaired (Upd), leading to a concomitant loss of germline stem cells. Here we demonstrate that IGF-II messenger RNA binding protein (Imp) counteracts endogenous small interfering RNAs to stabilize upd (also known as os) RNA. However, similar to upd, Imp expression decreases in the hub cells of older males, which is due to the targeting of Imp by the heterochronic microRNA let-7. In the absence of Imp, upd mRNA therefore becomes unprotected and susceptible to degradation. Understanding the mechanistic basis for ageing-related changes in stem-cell behaviour will lead to the development of strategies to treat age-onset diseases and facilitate stem-cell-based therapies in older individuals.
成体干细胞在个体的一生中支持组织稳态和修复。随着年龄的增长,会发生许多内在和外在的变化,导致干细胞行为改变,组织维持和再生减少。在果蝇的睾丸中,衰老导致未配对(Upd)自我更新因子的显著减少,从而导致生殖干细胞的丧失。在这里,我们证明 IGF-II 信使 RNA 结合蛋白(Imp)与内源性小干扰 RNA 对抗,以稳定 upd(也称为 os)RNA。然而,与 upd 相似,Imp 的表达在年老雄性的枢纽细胞中下降,这是由于 Imp 被异型 microRNA let-7 靶向。在没有 Imp 的情况下,upd mRNA 因此变得没有保护,容易降解。了解与衰老相关的干细胞行为变化的机制基础将导致开发治疗与年龄相关疾病的策略,并促进老年个体的基于干细胞的治疗。