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Overexpression of APRIN inhibits differentiation and proliferation and promotes apoptosis in P19 embryonal carcinoma cells

机译:APRIN的过表达抑制P19胚胎癌细胞的分化和增殖并促进其凋亡

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摘要

We have previously demonstrated that androgen-induced proliferation inhibitor (APRIN) expression was upregulated in ventricular septum tissues from patients with ventricular septal defect (VSD). The present study was designed to investigate the effects of APRIN on P19 cell differentiation, proliferation and apoptosis. In this study, we established a stable APRIN-overexpressing P19 embryonal carcinoma cell line that can differentiate into myocardial cells when treated with 1 % dimethyl sulfoxide. Ourdata showed that mRNA expressions of myocardial cell differentiation-related genes (such as cTnT, α-MHC, GATA4, and MEF2C) in the APRIN-overexpressing P19 cells were downregulated compared to the empty-vector controls. Our findings also indicated that P19 cells overexpressing APRIN had a reduced growth rate and a decreased S phase of the cell cycle. Moreover, the apoptotic rate in P19 cells overexpressing APRIN was significantly higher than that in the controls. In conclusion, our study demonstrates that overexpression of APRIN inhibits differentiation and proliferation and promotes apoptosis in P19 cells, suggesting that APRIN may be involved in the pathogenesis of VSD.
机译:我们以前已经证明,患有室间隔缺损(VSD)的患者的室间隔组织中雄激素诱导的增殖抑制剂(APRIN)表达上调。本研究旨在研究APRIN对P19细胞分化,增殖和凋亡的影响。在这项研究中,我们建立了稳定的APRIN过表达的P19胚胎癌细胞系,当用1%二甲基亚砜处理时,它可以分化为心肌细胞。我们的数据表明,与空载体对照相比,过表达APRIN的P19细胞中心肌细胞分化相关基因(例如cTnT,α-MHC,GATA4和MEF2C)的mRNA表达下调。我们的发现还表明,过表达APRIN的P19细胞的生长速率降低且细胞周期的S期降低。此外,过表达APRIN的P19细胞的凋亡率显着高于对照。总之,我们的研究表明,APRIN的过表达抑制P19细胞的分化和增殖并促进其凋亡,这表明APRIN可能参与了VSD的发病机理。

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