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Effect of TPA on aquaporin 4 mRNA expression in cultured rat astrocytes
Author(s) -
Nakahama KenIchi,
Nagano Mamoru,
Fujioka Atsuko,
Shinoda Koh,
Sasaki Hiroshi
Publication year - 1999
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/(sici)1098-1136(19990201)25:3<240::aid-glia4>3.0.co;2-c
Subject(s) - cycloheximide , protein kinase c , astrocyte , biology , messenger rna , activator (genetics) , aquaporin 4 , microbiology and biotechnology , neuroglia , protein biosynthesis , endocrinology , biochemistry , kinase , receptor , central nervous system , gene
Aquaporin 4 (AQP4) is a predominant water channel protein in mammalian brains, localized in the astrocyte plasma membrane. The regulation of AQP4 is believed to be important for the homeostasis of water in the brain, but the AQP4 regulatory mechanisms are not yet known. In this study, we investigated the effect of a protein kinase C (PKC) activator on the expression of AQP4 mRNA in cultured rat astrocytes. Cultured rat astrocytes constitutively expressed AQP4 mRNA. Treatment of the cells with 0.1 μM of phorbol ester 12‐ O ‐tetradecanoylphorbol 13‐acetate (TPA), an activator of PKC, caused a rapid decrease in AQP4 mRNA. This effect was time‐ and dose‐dependent. The TPA‐induced decrease in AQP4 mRNA was inhibited by a relatively specific PKC inhibitor, 1‐(5‐isoquinoline sulfonyl)‐2‐methylpiperazine (H7) in a dose‐dependent manner. Moreover, prolonged treatment of the cells with TPA eliminated the subsequent decrease in AQP4 mRNA by TPA. These results strongly suggest that the TPA‐induced decrease in AQP4 mRNA is mediated by PKC activation. To test whether the effect of TPA requires protein synthesis, astrocytes were pretreated with cycloheximide, an inhibitor of protein synthesis. Pretreatment of the cells with cycloheximide did not inhibit the decrease in AQP4 mRNA induced by TPA. To test whether the TPA‐induced decrease in AQP4 was due to a decrease in the mRNA stability, we examined the effect of actinomycin D, an inhibitor of transcription, on TPA‐treated cells. The stability of AQP4 mRNA was not decreased by the pretreatment of the cells with actinomycin D. The results suggest that AQP4 mRNA is inhibited by TPA via PKC activation without de novo protein synthesis, and that the inhibition of AQP4 mRNA could be at the transcriptional level. GLIA 25:240–246, 1999. © 1999 Wiley‐Liss, Inc.