Ba Hoa Van, Reddy Bandugula Venkata, Hwang Inho
Department of Animal Science and BK21 PLUS program, Chonbuk National University, Jeonju, 561-756, South Korea.
In Vitro Cell Dev Biol Anim. 2015 May;51(5):447-54. doi: 10.1007/s11626-014-9849-8. Epub 2014 Dec 9.
Calpastatin participates in apoptotic cell death and cell signaling, but its role in skeletal myoblast development and molecular involvements in cell growth still remains unknown. The current study aimed to investigate the role of calpastatin on the expression patterns of calpains, caspases, and heat shock proteins (HSPs). In addition, the cell viability during myoblast growth under calpastatin silence condition was also investigated. Three small interference RNA sequences (siRNAs) were used to silence calpastatin gene and ligated into pSilencer plasmid vector to construct short hairpin RNA (shRNA) expression. The all three siRNAs significantly silence the calpastatin gene. Moreover, suppression of calpastatin significantly reduced the viability of myoblasts during growth phase when compared to control cells. Additionally, knockdown of calpastatin significantly increased the mRNA expression of μ-calpain, caspase-3, caspase-7, and caspase-9, as well as HSP-27, -70, and -90. The present study results suggested that the suppression of calpastatin resulted in the increased expression of μ-calpain, caspases, and HSPs which in turn regulate the apoptotic cell death. The present study throws light on the central role of calpastatin in the control of calpain activity, cell proliferation, cell survival, and apoptotic pathways.
钙蛋白酶抑制蛋白参与细胞凋亡性死亡和细胞信号传导,但其在骨骼肌成肌细胞发育中的作用以及在细胞生长中的分子机制仍不清楚。本研究旨在探讨钙蛋白酶抑制蛋白对钙蛋白酶、半胱天冬酶和热休克蛋白(HSPs)表达模式的影响。此外,还研究了钙蛋白酶抑制蛋白沉默条件下成肌细胞生长过程中的细胞活力。使用三个小干扰RNA序列(siRNAs)沉默钙蛋白酶抑制蛋白基因,并将其连接到pSilencer质粒载体中以构建短发夹RNA(shRNA)表达。所有这三种siRNAs均能显著沉默钙蛋白酶抑制蛋白基因。此外,与对照细胞相比,钙蛋白酶抑制蛋白的抑制显著降低了成肌细胞在生长阶段的活力。此外,钙蛋白酶抑制蛋白的敲低显著增加了μ-钙蛋白酶、半胱天冬酶-3、半胱天冬酶-7和半胱天冬酶-9以及HSP-27、-70和-90的mRNA表达。本研究结果表明,钙蛋白酶抑制蛋白的抑制导致μ-钙蛋白酶、半胱天冬酶和HSPs表达增加,进而调节细胞凋亡性死亡。本研究揭示了钙蛋白酶抑制蛋白在控制钙蛋白酶活性、细胞增殖、细胞存活和凋亡途径中的核心作用。