Tob1 的缺失可通过肌肉干细胞扩增促进肌肉再生。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-08-12 DOI:10.1242/jcs.261886
Yasuo Kitajima, Kiyoshi Yoshioka, Yoko Mikumo, Shun Ohki, Kazumitsu Maehara, Yasuyuki Ohkawa, Yusuke Ono
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引用次数: 0

摘要

肌肉干细胞(MuSCs)在出生后肌肉生长和成年肌肉肥大中发挥着不可或缺的作用。肌肉干细胞还具有很强的再生能力,因此被认为是肌肉疾病再生治疗的一种有前途的干细胞来源。在这项研究中,我们发现肿瘤抑制蛋白Tob1是一个Pax7靶基因,它能负向控制MuSCs的群体扩增。Tob1蛋白在静止状态下检测不到,但在MuSCs活化过程中会上调。在小鼠体内消减 Tob1 可加速肌肉干细胞的群体扩增并促进肌肉再生。此外,在小鼠肌肉萎缩症模型中,MuSCs 中的 Tob1 失活可提高 MuSC 移植的效率。总之,选择性靶向 Tob1 可能是治疗肌肉疾病(包括肌肉萎缩症和老年性肌肉疏松症)的一种治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Loss of Tob1 promotes muscle regeneration through muscle stem cell expansion.

Muscle stem cells (MuSCs) play an indispensable role in postnatal muscle growth and hypertrophy in adults. MuSCs also retain a highly regenerative capacity and are therefore considered a promising stem cell source for regenerative therapy for muscle diseases. In this study, we identify tumor-suppressor protein Tob1 as a Pax7 target protein that negatively controls the population expansion of MuSCs. Tob1 protein is undetectable in the quiescent state but is upregulated during activation in MuSCs. Tob1 ablation in mice accelerates MuSC population expansion and boosts muscle regeneration. Moreover, inactivation of Tob1 in MuSCs ameliorates the efficiency of MuSC transplantation in a murine muscular dystrophy model. Collectively, selective targeting of Tob1 might be a therapeutic option for the treatment of muscular diseases, including muscular dystrophy and age-related sarcopenia.

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CiteScore
7.20
自引率
4.30%
发文量
567
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