Korea University, Seoul, South Korea.
Cytokine. 2010 Apr;50(1):42-9. doi: 10.1016/j.cyto.2009.12.010. Epub 2010 Jan 25.
CKbeta8/CCL23 is a CC chemokine and alternative splicing of the CKbeta8 gene produces two mRNAs that encode CKbeta8 and its isoform CKbeta8-1. Chemokines play a critical role in leukocyte trafficking and development of inflammation and chemokines are also known to be involved in cell proliferation. To investigate participation of CKbeta8 and CKbeta8-1 in cell proliferation, we examined the effects of CKbeta8 and CKbeta8-1 in the cell cycle. Both CKbeta8 and CKbeta8-1 induced cell-cycle progression. We next investigated whether MAPKs are involved in CKbeta8- and CKbeta8-1-induced cell proliferation. CKbeta8- and CKbeta8-1-stimulated cells showed phosphorylation of ERK1/2 and an inhibitor study indicated that CKbeta8- and CKbeta8-1-induced activation of ERK1/2 is mediated by the G(i)/G(o) protein, PLC, and PKCdelta. CKbeta8 and CKbeta8-1 regulated expression of the cell cycle regulators cyclin D(3) and cyclin B(1,) and the immediate early response gene products c-Myc and Egr-1. These results indicate that both CKbeta8 and CKbeta8-1 are involved in cell proliferation by modulating the cell cycle regulators.
CKbeta8/CCL23 是一种 CC 趋化因子,CKbeta8 基因的选择性剪接产生两种 mRNA,分别编码 CKbeta8 和其同工型 CKbeta8-1。趋化因子在白细胞迁移和炎症发展中起着关键作用,趋化因子也被认为参与细胞增殖。为了研究 CKbeta8 和 CKbeta8-1 在细胞增殖中的参与,我们研究了 CKbeta8 和 CKbeta8-1 在细胞周期中的作用。CKbeta8 和 CKbeta8-1 均诱导细胞周期进程。接下来,我们研究了 MAPK 是否参与 CKbeta8-和 CKbeta8-1 诱导的细胞增殖。CKbeta8-和 CKbeta8-1 刺激的细胞显示 ERK1/2 的磷酸化,抑制剂研究表明 CKbeta8-和 CKbeta8-1 诱导的 ERK1/2 激活是通过 G(i)/G(o)蛋白、PLC 和 PKCdelta 介导的。CKbeta8 和 CKbeta8-1 调节细胞周期调节剂 cyclin D(3)和 cyclin B(1)的表达,以及即刻早期反应基因产物 c-Myc 和 Egr-1。这些结果表明,CKbeta8 和 CKbeta8-1 均通过调节细胞周期调节剂参与细胞增殖。