Wagshal A B, Jegasothy B V, Waksman B H
J Exp Med. 1978 Jan 1;147(1):171-81. doi: 10.1084/jem.147.1.171.
IDS inhibits DNA synthesis and mitosis of L cells only when present during the late G1 phase of the cell cycle, as shown with L cells synchronized by a variety of methods. This corresponds well with earlier findings that IDS inhibits DNA synthesis in mitogen-stimulated lymphocytes when present between 16 and 24 h after adding mitogen. In both cell types, the inhibition produced by IDS appears to be totally the result of elevation of cAMP level. Thus, inhibitors of cAMP phosphodiesterase work synergistically with IDS, and activators of cAMP phosphodiesterase overcome the inhibition by IDS. This paper shows that IDS raises cAMP levels in L cells only within a narrow interval of the cell cycle, around 6-8 h after mitosis. This cell cycle specificity, which may be related to appearance of receptors for IDS only at discrete times, may be important in limiting IDS action to suppression, as elevated cAMP levels have a variety of other effects during other phases of the cell cycle.
如通过多种方法同步化的L细胞所示,IDS仅在细胞周期的G1期晚期存在时才会抑制L细胞的DNA合成和有丝分裂。这与早期的研究结果非常吻合,即在添加促有丝分裂原后16至24小时之间存在时,IDS会抑制促有丝分裂原刺激的淋巴细胞中的DNA合成。在这两种细胞类型中,IDS产生的抑制作用似乎完全是cAMP水平升高的结果。因此,cAMP磷酸二酯酶抑制剂与IDS协同作用,而cAMP磷酸二酯酶激活剂则可克服IDS的抑制作用。本文表明,IDS仅在细胞周期的一个狭窄时间段内,即有丝分裂后约6 - 8小时,才会提高L细胞中的cAMP水平。这种细胞周期特异性可能与IDS受体仅在特定时间出现有关,这对于将IDS的作用限制在抑制方面可能很重要,因为在细胞周期的其他阶段,cAMP水平升高会产生多种其他影响。