Department of Physiological Sciences and Biochemistry, Stellenbosch University, Matieland 7602, Stellenbosch, South Africa.
International Centre for Genetic Engineering and Biotechnology (ICGEB), Cape Town Component and Institute of Infectious Disease and Molecular Medicine, Wernher and Beit Building (South), University of Cape Town Medical Campus, Anzio Road, Observatory 7925, Cape Town, South Africa.
Int J Mol Sci. 2019 Oct 24;20(21):5273. doi: 10.3390/ijms20215273.
Postnatal muscle growth and exercise- or injury-induced regeneration are facilitated by myoblasts. Myoblasts respond to a variety of proteins such as cytokines that activate various signaling cascades. Cytokines belonging to the interleukin 6 superfamily (IL-6) influence myoblasts' proliferation but their effect on differentiation is still being researched. The Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway is one of the key signaling pathways identified to be activated by IL-6. The aim of this study was to investigate myoblast fate as well as activation of JAK-STAT pathway at different physiologically relevant IL-6 concentrations (10 pg/mL; 100 pg/mL; 10 ng/mL) in the C2C12 mouse myoblast cell line and primary human myoblasts, isolated from eight young healthy male volunteers. Myoblasts' cell cycle progression, proliferation and differentiation in vitro were assessed. Low IL-6 concentrations facilitated cell cycle transition from the quiescence/Gap1 (G0/G1) to the synthesis (S-) phases. Low and medium IL-6 concentrations decreased the expression of myoblast determination protein 1 (MyoD) and myogenin and increased proliferating cell nuclear antigen (PCNA) expression. In contrast, high IL-6 concentration shifted a larger proportion of cells to the pro-differentiation G0/G1 phase of the cell cycle, substantiated by significant increases of both MyoD and myogenin expression and decreased PCNA expression. Low IL-6 concentration was responsible for prolonged JAK1 activation and increased suppressor of cytokine signaling 1 (SOCS1) protein expression. JAK-STAT inhibition abrogated IL-6-mediated C2C12 cell proliferation. In contrast, high IL-6 initially increased JAK1 activation but resulted in prolonged JAK2 activation and elevated SOCS3 protein expression. High IL-6 concentration decreased interleukin-6 receptor (IL-6R) expression 24 h after treatment whilst low IL-6 concentration increased IL-6 receptor (IL-6R) expression at the same time point. In conclusion, this study demonstrated that IL-6 has concentration- and time-dependent effects on both C2C12 mouse myoblasts and primary human myoblasts. Low IL-6 concentration induces proliferation whilst high IL-6 concentration induces differentiation. These effects are mediated by specific components of the JAK/STAT/SOCS pathway.
成肌细胞促进产后肌肉生长和运动或损伤诱导的再生。成肌细胞对各种蛋白质(如细胞因子)作出反应,这些蛋白质激活各种信号级联。白细胞介素 6 超家族(IL-6)中的细胞因子影响成肌细胞的增殖,但它们对分化的影响仍在研究中。Janus 激酶(JAK)-信号转导和转录激活因子(STAT)途径是被鉴定为被 IL-6 激活的关键信号通路之一。本研究的目的是研究在 C2C12 小鼠成肌细胞系和从 8 名年轻健康男性志愿者中分离的原代人成肌细胞中,不同生理相关 IL-6 浓度(10pg/ml;100pg/ml;10ng/ml)下成肌细胞的命运以及 JAK-STAT 途径的激活。在体外评估了成肌细胞的细胞周期进程、增殖和分化。低浓度的 IL-6 促进细胞从静止/间隙 1(G0/G1)期向合成(S)期的过渡。低浓度和中浓度的 IL-6 降低了成肌细胞决定蛋白 1(MyoD)和成肌生成素的表达,并增加了增殖细胞核抗原(PCNA)的表达。相比之下,高浓度的 IL-6 将更大比例的细胞转移到细胞周期的促分化 G0/G1 期,这一点通过 MyoD 和成肌生成素表达的显著增加和 PCNA 表达的降低得到证实。低浓度的 IL-6 负责延长 JAK1 的激活并增加细胞因子信号转导抑制因子 1(SOCS1)蛋白的表达。JAK-STAT 抑制消除了 IL-6 介导的 C2C12 细胞增殖。相反,高浓度的 IL-6 最初增加了 JAK1 的激活,但导致 JAK2 的长期激活和 SOCS3 蛋白表达的升高。高浓度的 IL-6 在治疗后 24 小时降低白细胞介素 6 受体(IL-6R)的表达,而低浓度的 IL-6 在同一时间点增加 IL-6 受体(IL-6R)的表达。总之,本研究表明,IL-6 对 C2C12 小鼠成肌细胞和原代人成肌细胞具有浓度和时间依赖性的影响。低浓度的 IL-6 诱导增殖,而高浓度的 IL-6 诱导分化。这些作用是通过 JAK/STAT/SOCS 途径的特定成分介导的。