E3连接酶Trim63通过催化K27-linked半胱氨酸泛素化Myh11促进间充质干细胞的软骨分化。

IF 4 2区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
STEM CELLS Pub Date : 2025-04-29 DOI:10.1093/stmcls/sxaf017
Shanyu Ye, Yanqing Wang, Ziwei Luo, Aijun Liu, Xican Li, Jiasong Guo, Wei Zhao, Dongfeng Chen, Lin Yang, Helu Liu
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引用次数: 0

摘要

间充质干细胞(MSCs)是具有软骨分化能力的多能干细胞。然而,MSCs成软骨分化的分子机制尚未完全阐明,这阻碍了临床中基于MSCs的软骨修复细胞疗法的进一步发展。在这里,我们发现E3泛素连接酶Trim63通过催化K27-linked半胱氨酸泛素化Myh11正向调节MSCs的软骨分化。Trim63直接与Myh11相互作用并催化k27连接的cys382泛素化。cys382突变减少了trim63催化的k27连接的泛素化和MSCs的软骨分化。Trim63缺乏会显著损害间充质干细胞的软骨分化。Trim63在体内促进关节软骨缺损的修复。综上所述,我们的研究结果表明,Trim63通过催化Myh11的K27-linked半胱氨酸泛素化促进MSCs的软骨分化,这为软骨再生和修复提供了另一种治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
E3 ligase Trim63 promotes the chondrogenic differentiation of mesenchymal stem cells by catalyzing K27-linked cysteine ubiquitination of Myh11.

Mesenchymal stem cells (MSCs) are multipotent stem cells that have a chondrogenic differentiation capacity. However, the molecular mechanism underlying the chondrogenic differentiation of MSCs has not been fully elucidated, which hinders further development of MSC-based cell therapies for cartilage repair in the clinic. Here, we showed that the E3 ubiquitin ligase Trim63 positively regulates the chondrogenic differentiation of MSCs by catalyzing K27-linked cysteine ubiquitination of Myh11. Trim63 directly interacts with Myh11 and catalyzes K27-linked ubiquitination of cys382. Mutation of cys382 diminishes Trim63-catalyzed K27-linked ubiquitination and chondrogenic differentiation of MSCs. A deficiency in Trim63 significantly impairs the chondrogenic differentiation of MSCs. Trim63 enhances the repair of articular cartilage defects in vivo. Taken together, the results of our study demonstrated that Trim63 promotes the chondrogenic differentiation of MSCs by catalyzing K27-linked cysteine ubiquitination of Myh11, which provides an alternative therapeutic target for cartilage regeneration and repair.

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来源期刊
STEM CELLS
STEM CELLS 医学-生物工程与应用微生物
CiteScore
10.30
自引率
1.90%
发文量
104
审稿时长
3 months
期刊介绍: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. STEM CELLS is read and written by clinical and basic scientists whose expertise encompasses the rapidly expanding fields of stem and progenitor cell biology. STEM CELLS covers: Cancer Stem Cells, Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells, Regenerative Medicine, Stem Cell Technology: Epigenetics, Genomics, Proteomics, and Metabonomics, Tissue-Specific Stem Cells, Translational and Clinical Research.
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