首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Proteomic study of calpeptin-induced differentiation on calpain-interacting proteins of C2C12 myoblast
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Proteomic study of calpeptin-induced differentiation on calpain-interacting proteins of C2C12 myoblast

机译:钙蛋白酶对C2C12成肌细胞钙蛋白酶相互作用蛋白诱导分化的蛋白质组学研究

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摘要

Studies on skeletal muscle cell specification and development have demonstrated in the past that calpains interact with various transcriptional factors in regulating the cellular function. It has therefore, been assumed that transcriptional factors like myogenin, MyoD, Myf5, and MRF4 that are active during the myogenic differentiation might be affected and degraded by calpains. Therefore, to examine the biochemical adaptations of myoblasts during myocyte formation and muscle development comprehensively, the current study was designed to identify the effect of calpeptin (calpain inhibitors) on protein expression during differentiation of C2C12 mouse myoblast. Cells were proliferated to near 80% confluence under Dulbecco's modified eagle medium and differentiated further in 2% HS with 50 mu M calpeptin. Incubated cells were collected at 0, 12, and 72 h and later the cell proteins were focused onto pH 4-7 IEF strip, followed by 12.5% SDS-PAGE. Obtained spots on the gels were compared and matched using commercial 2-DE analysis software and matched spots were identified by MALDI-ToF and/or Q-Tof systems. Conclusively, cell differentiation was observed to be active from 12 to 72 h however, calpeptin affected the differentiation process and cut down the rate of fusion by approximately 50%. Out of 41 proteins identified, 12 proteins were found to be upregulated where as 29 proteins were downregulated.
机译:过去,对骨骼肌细胞规格和发育的研究表明,钙蛋白酶与多种转录因子相互作用,调节细胞功能。因此,已经假定,在肌原性分化期间活跃的转录因子,例如肌生成素,MyoD,Myf5和MRF4,可能会受到钙蛋白酶的影响和降解。因此,要全面检查成肌细胞在心肌细胞形成和肌肉发育过程中的生化适应性,本研究旨在鉴定钙蛋白酶(钙蛋白酶抑制剂)对C2C12小鼠成肌细胞分化过程中蛋白质表达的影响。在Dulbecco改良的Eagle培养基中,细胞增殖至接近80%汇合,并在含有50μM钙蛋白酶的2%HS中进一步分化。在0、12和72小时收集孵育的细胞,然后将细胞蛋白聚焦到pH 4-7 IEF条上,然后进行12.5%SDS-PAGE。比较凝胶上获得的斑点,并使用市售的2-DE分析软件进行匹配,并通过MALDI-ToF和/或Q-Tof系统鉴定匹配的斑点。最终,观察到细胞分化在12到72小时内是活跃的,但是,钙蛋白酶抑制了分化过程并使融合率降低了约50%。在鉴定出的41种蛋白质中,有12种蛋白质被上调,其中29种蛋白质被下调。

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