Key result
NET39 suppresses myoblast differentiation by reducing mTOR activity and IGF-II production.
Why the study?
The role of the nuclear envelope protein NET39 in regulating myoblast differentiation and its mechanisms were not fully understood.
NET39 functions as a negative regulator of myoblast differentiation by modulating mTOR signaling and IGF-II production, suggesting a role in muscle homeostasis.
NET39 inhibition may enhance myoblast differentiation; hypothesis-generating for muscle regeneration in cardiovascular disease.
Recently, several transmembrane proteins of the nuclear envelope have been implicated in regulation of signaling and gene expression. Here we demonstrate that the nuclear lamina-associated nuclear envelope transmembrane protein NET39 (Ppapdc3) functions as a negative regulator of myoblast differentiation, in part through effects on mTOR signaling. We found that NET39 is highly expressed in cardiac and skeletal muscle tissues and becomes strongly upregulated during cultured myoblast differentiation. Knockdown of NET39 by RNA interference in myoblasts strongly promoted differentiation, whereas overexpression of NET39 repressed myogenesis. Proteomic analysis of NET39 complexes immunoprecipitated from myotubes, in combination with other methods, identified mTOR as an interaction partner of NET39. We found that ectopic expression of NET39 in myoblasts negatively regulated myogenesis by diminishing mTOR activity, which in turn decreased insulin-like growth factor II production and autocrine signaling. Our results indicate that NET39 is part of the regulatory machinery for myogenesis and raise the possibility that it may be important for muscle homeostasis.
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Liu et al. (2009) studied this question. NET39 knockdown and overexpression was evaluated on Myoblast differentiation and mTOR signaling. NET39 functions as a negative regulator of myoblast differentiation by diminishing mTOR activity and decreasing insulin-like growth factor II production.
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