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一氧化氮抑制培养的大鼠肝细胞中的DNA合成并诱导聚(ADP-核糖)聚合酶的激活。

Nitric oxide inhibits DNA synthesis and induces activation of poly(ADP-ribose) polymerase in cultured rat hepatocytes.

作者信息

Dalmau M, Joaquin M, Nakamura T, Bartrons R, Gil J

机构信息

Facultat d'Odontologia, Universitat de Barcelona, Spain.

出版信息

Exp Cell Res. 1996 Oct 10;228(1):14-8. doi: 10.1006/excr.1996.0293.

Abstract

Incubation of cultured rat hepatocytes with sodium nitroprusside or SIN-1, two nitric oxide (NO) donors, inhibited the mitogenic action of hepatocyte growth factor in a dose-dependent manner. The addition of 100 microM reduced hemoglobin, which is known to absorb NO, or the presence of 20 microM 1,5-isoquinolinediol, a poly(ADP-ribose) polymerase (PARP) inhibitor, decreased the cytostatic effects of SIN-1. By labeling the hepatocytes with [2-3H]adenine we studied whether nitric oxide induces ADP-ribosylation of proteins in a whole-cell system. At 0.4 mM, sodium nitroprusside increased the [3H]adenine labeling of two proteins of 116 and 130-135 kDa. This effect was time-dependent and was detected after 2 h. Only the 116-kDa protein was recognized by three different antibodies against poly (ADP-ribose) polymerase in Western blot assays. These results demonstrate that NO has antimitogenic effects in cultured hepatocytes and that its action could be mediated by PARP activation.

摘要

用两种一氧化氮(NO)供体硝普钠或SIN - 1孵育培养的大鼠肝细胞,可剂量依赖性地抑制肝细胞生长因子的促有丝分裂作用。添加已知能吸收NO的100微摩尔还原血红蛋白,或存在20微摩尔1,5 - 异喹啉二醇(一种聚(ADP - 核糖)聚合酶(PARP)抑制剂),可降低SIN - 1的细胞生长抑制作用。通过用[2 - 3H]腺嘌呤标记肝细胞,我们研究了一氧化氮是否在全细胞系统中诱导蛋白质的ADP - 核糖基化。在0.4毫摩尔时,硝普钠增加了两种分子量分别为116 kDa和130 - 135 kDa蛋白质的[3H]腺嘌呤标记。这种效应具有时间依赖性,在2小时后即可检测到。在蛋白质印迹分析中,只有116 kDa的蛋白质能被三种不同的抗聚(ADP - 核糖)聚合酶抗体识别。这些结果表明,NO在培养的肝细胞中具有抗有丝分裂作用,其作用可能由PARP激活介导。

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