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T51B大鼠肝上皮样细胞通过环磷酸腺苷依赖性启动DNA合成。

The cyclic AMP-dependent initiation of DNA synthesis by T51B rat liver epithelioid cells.

作者信息

Boynton A L, Whitfield J F

出版信息

J Cell Physiol. 1979 Oct;101(1):139-48. doi: 10.1002/jcp.1041010116.

Abstract

The brief rise in the cellular cyclic AMP content which occurs late in the prereplicative phases of rat hepatocytes in vivo and T51B rat liver epitheloid cells in vitro seems to be necessary for the initiation of DNA synthesis. Thus, the extracellular calcium-deprivation in T51B rat liver cells in culture which induces a late G-1 block is rapidly reversible (cells surge into S phase within one hour) either by creating a cyclic AMP surge by the addition of calcium or 3-isobutyl-1-methyl xanthine (a cyclic 3',5'-nucleotide phosphodiesterase inhibitor) or by the exogenous addition of low concentrations of cyclic AMP itself (i.e., 10(-8)-10(-5) M). On the other hand, prevention of the calcium-induced cyclic AMP surge by imidazole (a cyclic 3',5'-nucleotide phosphodiesterase activator) blocked the initiation of DNA synthesis by the calcium-deprived T51B cells.

摘要

在体内大鼠肝细胞和体外T51B大鼠肝上皮样细胞复制前阶段后期出现的细胞内环磷酸腺苷(cAMP)含量短暂升高,似乎是DNA合成起始所必需的。因此,培养的T51B大鼠肝细胞中的细胞外钙剥夺会诱导G-1期晚期阻滞,这种阻滞可通过以下方式迅速逆转(细胞在一小时内进入S期):添加钙或3-异丁基-1-甲基黄嘌呤(一种环3',5'-核苷酸磷酸二酯酶抑制剂)以产生cAMP激增,或者外源添加低浓度的cAMP本身(即10(-8)-10(-5) M)。另一方面,咪唑(一种环3',5'-核苷酸磷酸二酯酶激活剂)阻止钙诱导的cAMP激增,从而阻断了钙剥夺的T51B细胞的DNA合成起始。

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