Wieteska-Skrzeczyńska W, Grzelkowska-Kowalczyk K, Tokarska J, Grabiec K
Department of Physiological Sciences, Faculty of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland.
Pol J Vet Sci. 2011;14(3):417-24. doi: 10.2478/v10181-011-0062-3.
The aim of this study was to examine the potential interactions of IGF-I with TNF-alpha and IFN-gamma with regard to regulation of the myogenesis and proliferative potential of mouse C2C12 myoblasts. The stimulation of myogenesis by IGF-I (30 nmol/l) was manifested by an enhanced myoblast fusion and expression of myosin heavy chain (MHC) during the first 3 days of differentiation. IGF-I-dependent fusion and MHC expression was reduced by TNF-alpha and IFN-gamma. Both cytokines prevented the stimulatory effect of IGF-I on MyoD expression with minor modification of the myogenin level. Both TNF-alpha and IFN-gamma activated the expression of cyclin A in myoblasts restimulated to proliferation; however, when used in combination with IGF-I these cytokines prevented the rise in cyclin A induced by growth factor.
i) TNF-alpha and IFN-gamma reduce IGF-I-dependent myogenesis which was manifested by the reduction of myoblast fusion and MHC cellular levels, ii) Molecular mechanisms of inhibitory action of TNF-alpha and IFN-gamma on IGF-I-mediated differentiation involve a decrease in MyoD whereas myogenin level plays a minor role, iii) TNF-alpha and IFN-gamma increase the proliferative potential of myoblasts; however, they reduced the mitogenic effect of IGF-I, manifested by a decrease of IGF-I-stimulated cyclin A expression in myoblasts reinduced to proliferation. Interactions among IGF-I and proinflammatory cytokines are therefore important to establish a number of myoblasts and the onset of myogenesis during muscle regeneration.
本研究的目的是探讨胰岛素样生长因子-I(IGF-I)与肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)在调节小鼠C2C12成肌细胞的肌生成和增殖潜能方面的潜在相互作用。IGF-I(30 nmol/l)对肌生成的刺激表现为在分化的前3天成肌细胞融合增强和肌球蛋白重链(MHC)表达增加。TNF-α和IFN-γ降低了IGF-I依赖的融合和MHC表达。两种细胞因子均轻微改变肌细胞生成素水平,同时阻止了IGF-I对肌分化抗原(MyoD)表达的刺激作用。TNF-α和IFN-γ均激活了重新刺激增殖的成肌细胞中细胞周期蛋白A的表达;然而,当与IGF-I联合使用时,这些细胞因子阻止了生长因子诱导的细胞周期蛋白A的升高。
i)TNF-α和IFN-γ降低了IGF-I依赖的肌生成,表现为成肌细胞融合和MHC细胞水平降低;ii)TNF-α和IFN-γ对IGF-I介导的分化的抑制作用的分子机制涉及MyoD减少,而肌细胞生成素水平起次要作用;iii)TNF-α和IFN-γ增加了成肌细胞的增殖潜能;然而,它们降低了IGF-I的促有丝分裂作用,表现为重新诱导增殖的心机细胞中IGF-I刺激的细胞周期蛋白A表达减少。因此,IGF-I与促炎细胞因子之间的相互作用对于在肌肉再生过程中确定成肌细胞数量和肌生成的起始非常重要。