Inhibition by Protein Kinase C Inhibitor of Expression of Leukocyte Function-associated Antigen-1 Molecules in Rat Hepatoma AH66F Cells |
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Authors: | Masaaki Nomura Norihiko Sugiura Shuzo Moritani Ken-ichi Miyamoto |
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Affiliation: | Department of Applied Pharmacology, Faculty of Pharmaceutical Sciences, Hokuriku University, Ho-3 Kanagawa-machi, Kanazawa 920–11;Fukui Prefectural University College of Nursing, 4–1-1 Kenjojima, Matsuoka-cho, Fukui 910–11;Department of Pharmacology and Pharmaceutics, Graduate School of Pharmaceutical Sciences, Kanazawa University, 13–1 Takara-machi, Kanazawa 920 |
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Abstract: | To examine the mechanism of inhibition by protein kinase C (PKC) inhibitors of the adhesion of highly malignant hepatoma AH66F cells to the mesentery-derived mesothelial cell (M-cell) layer through leukocyte function-associated antigen-1 (LFA-1)/intercellular adhesion molecule-1, the effects of a PKC inhibitor, NA-382, on the expression of LFA-1 molecules in AH66F cells were examined and compared with those in thymocytes from normal rats. NA-382 inhibited the adhesion of AH66F cells to the M-cell layer and the expression of LFA-1 on the membrane of the hepatoma cells after treatment for more than 24 h. It was confirmed that AH66F cells express similar mRNAs for LFA-1 subunits to those of thymocytes, and their levels were also decreased after treatment with NA-382. On the other hand, the LFA-1-mediated adhesion and the expression of both protein and mRNA for LFA-1 subunits in thymocytes were not changed by the PKC inhibitor. These results suggest that the expression of LFA-1 molecules in AH66F cells may be regulated by PKC via quite different mechanisms from those in normal lymphocytes |
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Keywords: | Rat hepatoma AH66F cell LFA-1 mRNA Expression Protein kinase C inhibitor |
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