| Literature DB >> 30917318 |
Xiaoqing Ren1, Boqiang Hu2, Moshi Song3, Zhichao Ding4, Yujiao Dang2, Zunpeng Liu5, Weiqi Zhang6, Qianzhao Ji4, Ruotong Ren7, Jianjian Ding8, Piu Chan9, Changtao Jiang10, Keqiong Ye11, Jing Qu12, Fuchou Tang13, Guang-Hui Liu14.
Abstract
CBX4, a component of polycomb repressive complex 1 (PRC1), plays important roles in the maintenance of cell identity and organ development through gene silencing. However, whether CBX4 regulates human stem cell homeostasis remains unclear. Here, we demonstrate that CBX4 counteracts human mesenchymal stem cell (hMSC) aging via the maintenance of nucleolar homeostasis. CBX4 protein is downregulated in aged hMSCs, whereas CBX4 knockout in hMSCs results in destabilized nucleolar heterochromatin, enhanced ribosome biogenesis, increased protein translation, and accelerated cellular senescence. CBX4 maintains nucleolar homeostasis by recruiting nucleolar protein fibrillarin (FBL) and heterochromatin protein KRAB-associated protein 1 (KAP1) at nucleolar rDNA, limiting the excessive expression of rRNAs. Overexpression of CBX4 alleviates physiological hMSC aging and attenuates the development of osteoarthritis in mice. Altogether, our findings reveal a critical role of CBX4 in counteracting cellular senescence by maintaining nucleolar homeostasis, providing a potential therapeutic target for aging-associated disorders.Entities:
Keywords: CBX4; CRISPR/Cas9; aging; epigenetics; gene editing; heterochromatin; nucleolus; osteoarthritis; rDNA; stem cell
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Year: 2019 PMID: 30917318 DOI: 10.1016/j.celrep.2019.02.088
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423