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无调性同源物8/数学相关转录因子6调控骨骼肌的分化与维持。

Atonal homolog 8/Math6 regulates differentiation and maintenance of skeletal muscle.

作者信息

Divvela Satya Srirama Karthik, Offei Eric Bekoe, Suerland Florian, Revuelta García David, Kwiatkowski Julia, Balakrishnan-Renuka Ajeesh, Bohne Pauline, Böing Marion, Morosan-Puopolo Gabriela, Mark Melanie D, Brand-Saberi Beate

机构信息

Department of Anatomy and Molecular Embryology, Medical Faculty, Ruhr-University Bochum, Bochum, Germany.

University of Ghana, School of Veterinary Medicine, Legon, Ghana.

出版信息

Front Cell Dev Biol. 2022 Aug 16;10:950414. doi: 10.3389/fcell.2022.950414. eCollection 2022.

Abstract

Atonal Homolog 8 (Atoh8) belongs to a large superfamily of transcriptional regulators called basic helix-loop-helix (bHLH) transcription factors. Atoh8 (murine homolog "Math6") has been shown to be involved in organogenesis during murine embryonic development. We have previously identified the expression of Atoh8 during skeletal myogenesis in chicken where we described its involvement in hypaxial myotome formation suggesting a regulatory role of Atoh8 in skeletal muscle development. Within the current study, we analyzed the effect of the loss of function of Atoh8 in murine primary myoblasts and during differentiation of pluripotent stem cells into myotubes, and the effect of its gain of function in C2C12 cells. Based on the observed results, we conclude that Atoh8 regulates myoblast proliferation via modulating myostatin signaling. Further, our data revealed a reduced muscle mass, strength and fiber size with significant changes to the muscle fiber type suggesting atrophy in skeletal muscle of Atoh8 mutants. We further report that Atoh8 knockout mice suffer from a condition similar to ambient hypoxia which may be the primary cause of the phenotype. Altogether, this study shows the significance of Atoh8 not only in myogenesis but also in the maintenance of skeletal muscle.

摘要

无调性同源物8(Atoh8)属于一个名为碱性螺旋-环-螺旋(bHLH)转录因子的转录调节因子大家族。Atoh8(小鼠同源物“Math6”)已被证明在小鼠胚胎发育过程中参与器官形成。我们之前已确定Atoh8在鸡骨骼肌生成过程中的表达情况,并描述了其在体轴下肌节形成中的作用,这表明Atoh8在骨骼肌发育中具有调节作用。在本研究中,我们分析了Atoh8功能丧失对小鼠原代成肌细胞以及多能干细胞分化为肌管过程的影响,以及其功能获得对C2C12细胞的影响。基于观察结果,我们得出结论,Atoh8通过调节肌生成抑制素信号来调控成肌细胞增殖。此外,我们的数据显示Atoh8突变体的骨骼肌出现肌肉质量、力量和纤维大小降低,且肌肉纤维类型发生显著变化,提示出现萎缩。我们进一步报告称,Atoh8基因敲除小鼠患有类似于环境性缺氧的病症,这可能是该表型的主要原因。总之,本研究表明Atoh8不仅在肌生成中具有重要意义,在骨骼肌维持方面也具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8538/9438786/319d17d56116/fcell-10-950414-g001.jpg

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