Li Yuwen, Jin Xinrong, Yu Chunyu, Zuo Min, Hong Liquan, Wang Mingwei, Zhao Chenyan, Wu Aiwei, Wang Jianjun, Ju Zhenyu, Wang Hu
Zhejiang Key Laboratory of Medical Epigenetics, School of Basic Medical Sciences, The Third People's Hospital of Deqing, Department of Cardiology, Affiliated Hospital of Hangzhou Normal University, Hangzhou Normal University, Hangzhou, China.
College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, China.
Commun Biol. 2025 May 1;8(1):688. doi: 10.1038/s42003-025-08071-2.
Phase separation, a biophysical process that segregates subcellular environments into condensates, has been recognized for its role in transcriptional regulation. However, the extent of its influence on cellular senescence processes remains to be fully elucidated. We established that MRG15 depletion leads to cellular senescence in human mesenchymal stem cells (hMSCs). MRG15 can form phase-separated liquid condensates via its intrinsically disordered region (IDR). IDR deletion and replacement assays revealed that MRG15 condensation is crucial to hMSC senescence. According to the epigenomic and transcriptomic analysis, MRG15 depletion impacts pathways integral to the cell cycle and the senescence process, as evidenced by the diminished binding and the modified expression of key genes, including p53, CDKN1A, LMNB1, CCNB1, NPM1, MYC, and HMGB2. Our findings establish a link between phase separation and senescence regulation and present a promising new therapeutic target for the alleviation of age-related diseases and the potential extension of lifespan.
相分离是一种将亚细胞环境分隔成凝聚物的生物物理过程,其在转录调控中的作用已得到认可。然而,其对细胞衰老过程的影响程度仍有待充分阐明。我们发现,MRG15的缺失会导致人间充质干细胞(hMSC)发生细胞衰老。MRG15可通过其内在无序区域(IDR)形成相分离的液体凝聚物。IDR缺失和替换试验表明,MRG15凝聚对hMSC衰老至关重要。根据表观基因组和转录组分析,MRG15的缺失影响细胞周期和衰老过程所必需的通路,关键基因p53、CDKN1A、LMNB1、CCNB1、NPM1、MYC和HMGB2的结合减少和表达改变证明了这一点。我们的研究结果建立了相分离与衰老调控之间的联系,并为缓解与年龄相关的疾病和潜在延长寿命提供了一个有前景的新治疗靶点。