Miller S C, Ito H, Blau H M, Torti F M
Department of Medicine, Stanford University Medical Center, California 94305.
Mol Cell Biol. 1988 Jun;8(6):2295-301. doi: 10.1128/mcb.8.6.2295-2301.1988.
We examined the effects of human recombinant tumor necrosis factor-alpha (TNF) on human primary myoblasts. When added to proliferating myoblasts, TNF inhibited the expression of alpha-cardiac actin, a muscle-specific gene whose expression is observed at low levels in human myoblasts. TNF also inhibited muscle differentiation as measured by several parameters, including cell fusion and the expression of other muscle-specific genes, such as alpha-skeletal actin and myosin heavy chain. Muscle cells were sensitive to TNF in a narrow temporal window of differentiation. Northern (RNA) blot and immunofluorescence analyses revealed that human muscle gene expression became unresponsive to TNF coincident with myoblast differentiation. When TNF was added to differentiated myotubes, there was no effect on muscle gene expression. In contrast, TNF-inducible mRNAs such as interferon beta-2 still responded, suggesting that the signal mediated by TNF binding to its receptor had no effect on muscle-specific genes after differentiation.
我们研究了重组人肿瘤坏死因子-α(TNF)对人原代成肌细胞的影响。当添加到增殖的成肌细胞中时,TNF抑制了α-心肌肌动蛋白的表达,α-心肌肌动蛋白是一种肌肉特异性基因,其在人成肌细胞中的表达水平较低。TNF还通过包括细胞融合以及其他肌肉特异性基因(如α-骨骼肌肌动蛋白和肌球蛋白重链)表达在内的几个参数来衡量,抑制了肌肉分化。肌肉细胞在分化的狭窄时间窗口内对TNF敏感。Northern(RNA)印迹和免疫荧光分析表明,随着成肌细胞分化,人肌肉基因表达对TNF不再有反应。当TNF添加到分化的肌管中时,对肌肉基因表达没有影响。相比之下,TNF诱导的mRNA如干扰素β-2仍然有反应,这表明TNF与其受体结合介导的信号在分化后对肌肉特异性基因没有影响。