Chou C F, Omary M B
Stanford University School of Medicine, Gastroenterology Division, CA 94305-5100.
FEBS Lett. 1991 Apr 22;282(1):200-4. doi: 10.1016/0014-5793(91)80477-k.
The phosphorylation of epithelial-specific cytokeratin (CK) 8 and 18 was studied in the human colonic cell line HT29. Metabolic labelling of cells with orthophosphate resulted in phosphorylation of cytokeratins 8/18 on serine residues. When phorbol acetate was added to labelled cells, a 2.2-fold increase in CK8/18 phosphate labelling was noted, whereas increasing intracellular cAMP levels using forskolin or 8-Br-cAMP showed no significant change in CK phosphorylation. CKs8/18 were also phosphorylated by added PKC in the presence of [gamma-32P]ATP. Tryptic peptide map analysis of the phosphorylated CK8 species showed that treatment of cells with 8-Br-cAMP or phorbol acetate generated a phosphopeptide not seen in control cells. In contrast, tryptic peptide maps of phosphorylated CK18 showed no discernable differences. Our results support a role for PKC in the phosphorylation of epithelial cytokeratins, with some phosphorylation sites being modulated by cAMP dependent protein kinase.
在人结肠癌细胞系HT29中研究了上皮特异性细胞角蛋白(CK)8和18的磷酸化。用正磷酸盐对细胞进行代谢标记导致细胞角蛋白8/18在丝氨酸残基上发生磷酸化。当将佛波酯添加到标记细胞中时,观察到CK8/18磷酸化标记增加了2.2倍,而使用福斯高林或8-溴-cAMP增加细胞内cAMP水平时,CK磷酸化没有显著变化。在[γ-32P]ATP存在下,添加的蛋白激酶C(PKC)也能使CKs8/18磷酸化。对磷酸化的CK8进行胰蛋白酶肽图谱分析表明,用8-溴-cAMP或佛波酯处理细胞会产生对照细胞中未出现的磷酸肽。相反,磷酸化的CK18的胰蛋白酶肽图谱没有明显差异。我们的结果支持PKC在上皮细胞角蛋白磷酸化中起作用,一些磷酸化位点受cAMP依赖性蛋白激酶调节。