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Okadaic acid strongly increases gene transcription, mRNA and protein level for the urokinase receptor in human A549 cells
Author(s) -
Lund Leif R.,
Danø Keld
Publication year - 1992
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(92)80050-q
Subject(s) - okadaic acid , activator (genetics) , microbiology and biotechnology , phosphatase , messenger rna , phosphorylation , protein kinase a , biology , urokinase receptor , transcription (linguistics) , chemistry , protein kinase c , gene , biochemistry , receptor , linguistics , philosophy
The specific phosphatase inhibitor, okadaic acid, increases the level of mRNA for the receptor for urokinase‐type plasminogen activator (u‐PAR) in 8 out of 13 human cell lines. The strongest increase (90‐fold) was observed in A549 lung carcinoma cells, in which it was partly traced back to an increased transcription of the u‐PAR gene. There was a parallel but less pronounced increase in the u‐PAR protein level. These findings indicate that u‐PAR gene transcription is regulated by one or more factors that are constitutively phosphorylated and are dephosphorylated by okadaic acid‐sensitive phosphatases. A lack of additivity of u‐PAR induction by okadaic acid and by the protein kinase C activator, PMA, in the A549 cells suggests that the regulatory factors affected by okadaic acid are phosphorylated by protein kinase C.