Ibrahim Musa, Alex Peter Seabright, Jonathan Barlow, Yusuke Nishimura
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引用次数: 0
摘要
肌环指蛋白1 (Muscle RING-finger protein 1, MuRF1,基因名:TRIM63)是骨骼肌萎缩的关键调控分子。尽管已经确定了MuRF1的几种底物和相互作用伙伴,但MuRF1导致骨骼肌萎缩的确切分子机制仍不清楚。为了进一步了解骨骼肌萎缩的潜在机制,我们采用靶向生化方法鉴定了含有三方基元的蛋白72 (TRIM72)作为一种新的murf1相互作用蛋白。随后通过MuRF1敲除和挽救实验分析表明,TRIM72蛋白丰度依赖于MuRF1蛋白的存在。此外,地塞米松治疗C2C12肌管中TRIM72蛋白水平升高,同时MuRF1蛋白水平升高。地塞米松降低野生型肌管中IRS1/Akt信号通路和葡萄糖摄取,但在MuRF1 KO肌管中没有。进一步分析发现,TRIM72的过表达会损害IRS1/Akt信号,而MuRF1不存在,这表明MuRF1可能通过与TRIM72的合作而对胰岛素信号传导产生负面影响。我们的发现提供了新的非降解的MuRF1分子作用,将骨骼肌萎缩和胰岛素敏感性受损联系在一起。
MuRF1 Partners With TRIM72 to Impair Insulin Signaling in Skeletal Muscle Cells
Muscle RING-finger protein 1 (MuRF1, gene name: TRIM63) is well known as a critical molecular regulator in skeletal muscle atrophy. Despite the identification of several substrates and interaction partners for MuRF1, the precise molecular mechanisms by which MuRF1 causes skeletal muscle atrophy remain unclear. To gain further insight into the underlying mechanism of skeletal muscle atrophy, we applied targeted biochemical approaches and identified tripartite motif-containing protein 72 (TRIM72) as a novel MuRF1-interacting protein. Subsequent analysis using MuRF1 knockout and rescue experiments showed that TRIM72 protein abundance is dependent on the presence of MuRF1 protein. Furthermore, TRIM72 protein level was increased by dexamethasone treatment in C2C12 myotubes, alongside increased MuRF1 protein level. Dexamethasone decreases IRS1/Akt signaling and glucose uptake specifically in wild type myotubes, but not in MuRF1 KO myotubes. Further analysis showed that overexpression of TRIM72 impairs IRS1/Akt signaling without the presence of MuRF1, indicating that MuRF1 induces a negative impact on insulin signaling through a plausible cooperation with TRIM72. Our findings provide novel non-degradative molecular roles of MuRF1 that link together skeletal muscle atrophy and impaired insulin sensitivity.
期刊介绍:
The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.