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Induction of apoptosis by the inhibitors of poly(ADP-ribose)polymerase in HeLa cells

机译:聚(ADP-核糖)聚合酶抑制剂诱导HeLa细胞凋亡

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摘要

To investigate the role of poly(ADP-ribose)polymerase (PARP) in the physiological condition of cell growth, we studied the ability of PARP inhibitors to induce apoptosis. Benzamide (BA) and 4-amino-1,8-naphthalimide (NAP), two well-known inhibitors of PARP, treatment increased nuclear fragmentation and caspase-3 activity in HeLa (Human cervical cancer cell line) cells. The increase of cellular NAD+ level was observed in HeLa cells treated with BA in comparison with untreated control cells. For unrevealing the specific PARP family member responsible for such induction of apoptosis we knocked down and over-expressed PARP-1 gene in HeLa cells. PARP-1 knock down cells were sensitive to BA induced nuclear fragmentation and caspase-3 activation while exogenous expression of PARP-1 rendered cells resistant to BA induced apoptosis. This result indicated that inhibition of PARP-1 resulted in induction of apoptosis.
机译:为了研究聚(ADP-核糖)聚合酶(PARP)在细胞生长生理状况中的作用,我们研究了PARP抑制剂诱导凋亡的能力。苯甲酰胺(BA)和4-氨基-1,8-萘二甲酰亚胺(NAP)是两种著名的PARP抑制剂,可治疗HeLa(人类宫颈癌细胞系)细胞的核分裂和caspase-3活性增加。与未处理的对照细胞相比,在用BA处理的HeLa细胞中观察到细胞NAD + 水平的增加。为了揭示负责这种凋亡诱导的特定PARP家族成员,我们在HeLa细胞中敲低了过表达的PARP-1基因。 PARP-1敲低细胞对BA诱导的核片段化和caspase-3激活敏感,而PARP-1的外源表达使细胞对BA诱导的凋亡具有抗性。该结果表明PARP-1的抑制导致凋亡的诱导。

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