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Inhibition of mammalian muscle differentiation by excretory secretory products of muscle larvae of Trichinella spiralis in vitro

机译:旋毛虫肌幼虫排泄分泌物对哺乳动物肌肉分化的抑制作用

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摘要

The excretory-secretory products (ESP) released by muscle stage of Trichinella spiralis have been suggested to be involved in nurse cell formation. However, the molecular mechanisms by which ESP modulate nurse cell formation remain unclear. In the present study, the ability of ESP of muscle larvae of T. spiralis (ML-ESP) to influence the proliferation and differentiation of murine myoblasts and the mechanisms were evaluated in vitro using C2C12 myoblast cell line, which were incubated for various times under grow or differentiation culture medium containing various concentrations of ML-ESP. The results indicated that ML-ESP promoted myoblast proliferation in a dose-dependent manner and increased the expression of the cell-cycle regulator cyclin D1 as well as that of proliferating cell nuclear antigen (PCNA). Conversely, ML-ESP inhibited the differentiation of these cells, which was evidenced by a reduction in the levels of MHC and MRFs expression (MyoD and myogenin) as well as that of p21. In addition, ML-ESP also inhibited the phosphorylation of p38 MAPK in differentiating C2C12 myoblast. Taken together, these results imply that certain critical mediators contained in ML-ESP inhibit myogenesis through enhancing skeletal myoblasts proliferation and down-regulating the expression of MRFs as well as involving p38 MAPK signalling pathway, which provides insight into the mechanisms utilised by T. spiralis to interfere normal wound repair in infected muscle cells and affect nurse cell formation.
机译:旋毛虫的肌肉阶段释放的排泄分泌产物(ESP)已被认为与护士细胞的形成有关。然而,ESP调节护士细胞形成的分子机制仍不清楚。在本研究中,螺旋藻肌肉幼虫的ESP(ML-ESP)影响鼠成肌细胞增殖和分化的能力及其机制在体外使用C2C12成肌细胞系进行了评估,该细胞系在C2C12下孵育了不同的时间。含有各种浓度的ML-ESP的生长或分化培养基。结果表明,ML-ESP以剂量依赖性方式促进成肌细胞增殖,并增加细胞周期调节剂cyclin D1和增殖细胞核抗原(PCNA)的表达。相反,ML-ESP抑制了这些细胞的分化,这通过降低MHC和MRFs(MyoD和肌生成素)以及p21的表达水平来证明。此外,ML-ESP还可以在分化C2C12成肌细胞中抑制p38 MAPK的磷酸化。综上所述,这些结果表明,ML-ESP中包含的某些关键介质通过增强骨骼肌成肌细胞增殖和下调MRFs的表达以及涉及p38 MAPK信号通路来抑制肌发生,从而提供了对螺旋螺旋体利用机制的深入了解。干扰感染的肌肉细胞的正常伤口修复并影响护士细胞的形成。

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