Gagelin C, Toru-Delbauffe D, Gavaret J M, Pierre M
Unité de Recherches Stéroïdes et Système Nerveux (U488 INSERM), Le Kremlin-Bicêtre, France.
J Neurochem. 1999 Nov;73(5):1799-805. doi: 10.1046/j.1471-4159.1999.0731799.x.
Cyclic AMP is a second messenger for various hormones that inhibits cell multiplication and DNA synthesis in cultured astrocytes. We examined the effects of increasing intracellular cyclic AMP on the catalytic (cdks) and regulatory (cyclins and ckis) components of cyclin-dependent protein kinases, which regulate progression of the cell cycle before completion of DNA synthesis, in primary cultured astrocytes and in an astrocytic cell line C.LT.T.1.1. The amount of cdk4 changed little during the cell cycle and was not affected by cyclic AMP. There was little cdk1 and cdk2 in quiescent cells, and their expression increased during the G1-S phases. Cyclic AMP strongly inhibited cdk1 and cdk2 expression. Transforming growth factor beta also inhibited cdk1 expression in primary astrocytes. Cyclic AMP did not affect the two ckis p27KIP1 and p21CIP1. There was little cyclin D1 in quiescent cells, but it increased during the G1 phase and was reduced by cyclic AMP. Cyclin E increased during the G1-S phases and was not affected by cyclic AMP in primary astrocytes. The amount of cyclin A was low in quiescent cells and increased during the G1-S phases. Expression of its mRNA and protein was inhibited by cyclic AMP. The protein kinase activities associated with complexes of cyclins and cdks were increased by growth factors and prevented by cyclic AMP. We conclude that cyclic AMP inhibits progression of the cell cycle in astrocytes at least by preventing the expression of the regulatory subunits, cyclins D1 and A, and catalytic subunits, cdk1 and cdk2, of cyclin-regulated protein kinases. Key Words: Cyclin-dependent protein kinases-Glial cells-Cyclic AMP.
环磷酸腺苷(Cyclic AMP)是多种激素的第二信使,可抑制培养的星形胶质细胞中的细胞增殖和DNA合成。我们研究了在原代培养的星形胶质细胞和星形胶质细胞系C.LT.T.1.1中,增加细胞内环磷酸腺苷对细胞周期蛋白依赖性蛋白激酶的催化成分(cdks)和调节成分(细胞周期蛋白和细胞周期蛋白依赖性激酶抑制剂)的影响,这些成分在DNA合成完成之前调节细胞周期进程。细胞周期蛋白依赖性激酶4(cdk4)的量在细胞周期中变化不大,且不受环磷酸腺苷的影响。静止细胞中细胞周期蛋白依赖性激酶1(cdk1)和细胞周期蛋白依赖性激酶2(cdk2)含量很少,它们的表达在G1-S期增加。环磷酸腺苷强烈抑制cdk1和cdk2的表达。转化生长因子β也抑制原代星形胶质细胞中cdk1的表达。环磷酸腺苷不影响两种细胞周期蛋白依赖性激酶抑制剂p27KIP1和p21CIP1。静止细胞中细胞周期蛋白D1(Cyclin D1)很少,但在G1期增加,并被环磷酸腺苷降低。细胞周期蛋白E(Cyclin E)在G1-S期增加,在原代星形胶质细胞中不受环磷酸腺苷影响。细胞周期蛋白A(Cyclin A)在静止细胞中的量较低,在G1-S期增加。其mRNA和蛋白质的表达被环磷酸腺苷抑制。与细胞周期蛋白和细胞周期蛋白依赖性激酶复合物相关的蛋白激酶活性被生长因子增加,并被环磷酸腺苷阻止。我们得出结论,环磷酸腺苷至少通过阻止细胞周期蛋白调节蛋白激酶的调节亚基细胞周期蛋白D1和A以及催化亚基cdk1和cdk2的表达来抑制星形胶质细胞中的细胞周期进程。关键词:细胞周期蛋白依赖性蛋白激酶 - 胶质细胞 - 环磷酸腺苷