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Yes 相关蛋白(Yap)在成年骨骼肌纤维中的组成性表达可诱导肌肉萎缩和肌病。

Constitutive expression of Yes-associated protein (Yap) in adult skeletal muscle fibres induces muscle atrophy and myopathy.

机构信息

School of Medicine and Dentistry, University of Aberdeen, Aberdeen, United Kingdom.

出版信息

PLoS One. 2013;8(3):e59622. doi: 10.1371/journal.pone.0059622. Epub 2013 Mar 27.

Abstract

The aim of this study was to investigate the function of the Hippo pathway member Yes-associated protein (Yap, gene name Yap1) in skeletal muscle fibres in vivo. Specifically we bred an inducible, skeletal muscle fibre-specific knock-in mouse model (MCK-tTA-hYAP1 S127A) to test whether the over expression of constitutively active Yap (hYAP1 S127A) is sufficient to drive muscle hypertrophy or stimulate changes in fibre type composition. Unexpectedly, after 5-7 weeks of constitutive hYAP1 S127A over expression, mice suddenly and rapidly lost 20-25% body weight and suffered from gait impairments and kyphosis. Skeletal muscles atrophied by 34-40% and the muscle fibre cross sectional area decreased by ≈40% when compared to control mice. Histological analysis revealed evidence of skeletal muscle degeneration and regeneration, necrotic fibres and a NADH-TR staining resembling centronuclear myopathy. In agreement with the histology, mRNA expression of markers of regenerative myogenesis (embryonic myosin heavy chain, Myf5, myogenin, Pax7) and muscle protein degradation (atrogin-1, MuRF1) were significantly elevated in muscles from transgenic mice versus control. No significant changes in fibre type composition were detected using ATPase staining. The phenotype was largely reversible, as a cessation of hYAP1 S127A expression rescued body and muscle weight, restored muscle morphology and prevented further pathological progression. To conclude, high Yap activity in muscle fibres does not induce fibre hypertrophy nor fibre type changes but instead results in a reversible atrophy and deterioration.

摘要

这项研究的目的是探究 Hippo 通路成员 Yes 相关蛋白(Yap,基因名 yap1)在体内骨骼肌纤维中的功能。具体而言,我们构建了一种可诱导的、骨骼肌纤维特异性的敲入小鼠模型(MCK-tTA-hYAP1 S127A),以测试组成性激活 Yap(hYAP1 S127A)的过表达是否足以驱动肌肉肥大或刺激纤维类型组成的变化。出乎意料的是,在持续 hYAP1 S127A 过表达 5-7 周后,小鼠突然迅速失去 20-25%的体重,并出现步态障碍和脊柱后凸。骨骼肌萎缩 34-40%,与对照小鼠相比,肌纤维横截面积减少约 40%。组织学分析显示出骨骼肌退化和再生、坏死纤维以及 NADH-TR 染色类似于核内肌病的证据。与组织学一致,转基因小鼠肌肉中再生肌发生的标志物(胚胎肌球蛋白重链、Myf5、肌生成素、Pax7)和肌肉蛋白降解(atrogin-1、MuRF1)的 mRNA 表达显著升高。使用 ATP 酶染色未检测到纤维类型组成的显著变化。该表型在很大程度上是可逆的,因为停止 hYAP1 S127A 表达挽救了体重和肌肉重量,恢复了肌肉形态并防止了进一步的病理进展。总之,肌纤维中 Yap 活性的增加不会诱导纤维肥大或纤维类型变化,而是导致可逆性萎缩和恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0bf/3609830/8a3d9be8f9db/pone.0059622.g001.jpg

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