Premium
Phorbol acetate enhances the phosphorylation of cytokeratins 8 and 18 in human colonic epithelial cells
Author(s) -
Chou C.-F.,
Omury M.Bishr
Publication year - 1991
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(91)80477-k
Subject(s) - phosphorylation , chemistry , microbiology and biotechnology , phorbol ester , biochemistry , biology , protein kinase c
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 [γ‐ 31 P]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 CK 18 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.