Kobayashi K, Phuchareon J, Inada K, Tomita Y, Koizumi T, Hatano M, Miyatake S, Tokuhisa T
Division of Developmental Genetics, Chiba University School of Medicine, Japan.
J Immunol. 1997 Mar 1;158(5):2050-6.
Splenic B cells activated by surface Ig (sIg) cross-linking transiently express the c-fos gene within 0.5 h and then enter into S phase of the cell cycle within 48 h. To investigate a role of c-fos in cell cycle progression, we used splenic B cells from IFN-alphabeta-inducible c-fos transgenic mice (Mx-c-fos). In the absence of IFN, the cell cycle progression of Mx-c-fos B cells stimulated with anti-IgM Ab was similar to that in control B cells. The cell cycle was arrested in G1 phase when we added IFN to the culture within 12 h after anti-IgM Ab stimulation, suggesting that overexpression of c-fos until mid-G1 phase perturbs activation of the cell cycle regulatory machinery. In control B cells, cyclin E and cdk2 were induced within 24 to 48 h after stimulation, and this induction was accompanied by down-regulation of a cdk2 inhibitor p27Kip1. As a consequence of these activation processes, cdk2 kinase activity was induced in B cells in the late G1 phase. However, kinase activity was not detected in Mx-c-fos B cells, presumably because the down-regulation of p27 was perturbed. These data suggest that c-Fos can negatively control cell cycle regulatory machinery in sIg-stimulated B cells.
通过表面免疫球蛋白(sIg)交联激活的脾B细胞在0.5小时内短暂表达c-fos基因,然后在48小时内进入细胞周期的S期。为了研究c-fos在细胞周期进程中的作用,我们使用了来自干扰素αβ诱导型c-fos转基因小鼠(Mx-c-fos)的脾B细胞。在没有干扰素的情况下,用抗IgM抗体刺激的Mx-c-fos B细胞的细胞周期进程与对照B细胞相似。当我们在抗IgM抗体刺激后12小时内向培养物中加入干扰素时,细胞周期停滞在G1期,这表明在G1中期之前c-fos的过表达会扰乱细胞周期调节机制的激活。在对照B细胞中,细胞周期蛋白E和细胞周期蛋白依赖性激酶2(cdk2)在刺激后24至48小时内被诱导,并且这种诱导伴随着cdk2抑制剂p27Kip1的下调。作为这些激活过程的结果,cdk2激酶活性在G1晚期的B细胞中被诱导。然而,在Mx-c-fos B细胞中未检测到激酶活性,推测是因为p27的下调受到了干扰。这些数据表明,c-Fos可以对sIg刺激的B细胞中的细胞周期调节机制产生负向控制作用。