Jin Caining, Ding Peiguo, Wang Ying, Ma Dalong
Lab of Medical Immunology, School of Basic Medical Science, Peking University Health Science Center, Peking University, No. 38 Xueyuan Road, Beijing 100083, China
FEBS Lett. 2005 Nov 21;579(28):6375-82. doi: 10.1016/j.febslet.2005.10.021. Epub 2005 Oct 24.
It is known that chemokine-like factor superfamily 8 (CKLFSF8), a member of the CKLF superfamily, has four putative transmembrane regions and a MARVEL domain. Its structure is similar to TM4SF11 (plasmolipin) and widely distributed in normal tissue. However, its function is not yet known. We show here that CKLFSF8 is associated with the epidermal growth factor receptor (EGFR) and that ectopic expression of CKLFSF8 in several cell lines suppresses EGF-induced cell proliferation, whereas knockdown of CKLFSF8 by siRNA promotes cell proliferation. In cells overexpressing CKLFSF8, the initial activation of EGFR was not affected, but subsequent desensitization of EGF-induced signaling occurred rapidly. This attenuation was correlated with an increased rate of receptor endocytosis. In contrast, knockdown of CKLFSF8 by siCKLFSF8 delayed EGFR endocytosis. These results identify CKLFSF8 as a novel regulator of EGF-induced signaling and indicate that the association of EGFR with four transmembrane proteins is critical for EGFR desensitization.
已知趋化因子样因子超家族8(CKLFSF8)是CKLF超家族的成员,具有四个推定的跨膜区域和一个MARVEL结构域。其结构与TM4SF11(质膜素)相似,广泛分布于正常组织中。然而,其功能尚不清楚。我们在此表明,CKLFSF8与表皮生长因子受体(EGFR)相关,并且CKLFSF8在几种细胞系中的异位表达抑制了EGF诱导的细胞增殖,而通过siRNA敲低CKLFSF8则促进细胞增殖。在过表达CKLFSF8的细胞中,EGFR的初始激活不受影响,但随后EGF诱导的信号脱敏迅速发生。这种衰减与受体内吞作用速率的增加相关。相反,通过siCKLFSF8敲低CKLFSF8延迟了EGFR内吞作用。这些结果确定CKLFSF8为EGF诱导信号的新型调节因子,并表明EGFR与四种跨膜蛋白的关联对于EGFR脱敏至关重要。