Foundational Sciences, College of Medicine, Central Michigan University, Mount Pleasant, MI, 48859, USA.
Department of Pathology, Icahn School of Medicine, One Gustave Levy Place, New York, NY, 10029, USA.
Differentiation. 2020 Jul-Aug;114:27-35. doi: 10.1016/j.diff.2020.05.001. Epub 2020 May 19.
Differentiation of cultured skeletal myoblasts is induced by extrinsic signals that include reduction in ambient mitogen concentration and increased cell density. Using an established murine myoblast cell line (C2C12), we have found that experimental reduction of the nucleoporin p62 (Nup62) content of myoblasts enhances differentiation in high-mitogen medium, while forced expression of Nup62 inhibits density-induced differentiation. In contrast, differentiation of myoblasts induced by low-mitogen medium was unaffected by ectopic Nup62 expression. Further analyses suggested that Nup62 content affects density-induced myoblast differentiation through a mechanism involving activation of p38 MAP kinase. Nuclear pore complex (NPC) composition, in particular changes in NUP62 content, may be altered during viral infection, differentiation, and in neoplastic growth. The results support a functional role for changes in Nup62 composition in NPCs and density-induced myogenic differentiation, and suggest a link between loss of Nup62 content and induction of an intracellular stress signaling pathways.
培养的骨骼肌成肌细胞的分化是由环境有丝分裂原浓度降低和细胞密度增加等外在信号诱导的。本研究使用已建立的鼠成肌细胞系(C2C12),发现实验性降低成肌细胞核孔蛋白 p62(Nup62)的含量可增强高有丝分裂原培养基中的分化,而强制表达 Nup62 则抑制密度诱导的分化。相比之下,低有丝分裂原培养基诱导的成肌细胞分化不受异位 Nup62 表达的影响。进一步的分析表明,Nup62 含量通过激活 p38 MAP 激酶的机制影响密度诱导的成肌细胞分化。核孔复合物(NPC)的组成,特别是 NUP62 含量的变化,可能在病毒感染、分化和肿瘤生长过程中发生改变。研究结果支持 NPC 中 Nup62 组成的变化以及密度诱导的成肌分化中的功能作用,并提示 Nup62 含量的丧失与细胞内应激信号通路的诱导之间存在联系。