Kawamura A, Yoshida Y, Kimura N, Oda H, Kakinuma A
Laboratory of Nutritional Biochemistry, Nagoya University, Nagoya, 464-8601, Japan.
Biochem Biophys Res Commun. 1999 Oct 22;264(2):530-6. doi: 10.1006/bbrc.1999.1544.
The effects of several protein kinase activators and protein phosphatase inhibitors on the phenobarbital (PB)-induced gene expression of CYP2B1 and CYP2B2 (CYP2B1/2B2) in adult rat hepatocytes were investigated. Insulin, epidermal growth factor, interleukin 6, cAMP, phorbol 12-myristate 13-acetate, tumor necrosis factor alpha, vanadate, and okadaic acid were found to suppress the induction of CYP2B1/2B2 at mRNA and protein levels in hepatocytes. cAMP and vanadate completely suppressed the induction of CYP2B1/2B2 gene expression in both rat hepatocytes and liver. The addition of genistein to vanadate-treated hepatocytes partially recovered the induction of CYP2B1/2B1 gene expression by PB. These results of the present study demonstrate that phosphorylation/dephosphorylation steps are crucial for the induction of CYP2B1/2B2 gene expression by PB.
研究了几种蛋白激酶激活剂和蛋白磷酸酶抑制剂对成年大鼠肝细胞中苯巴比妥(PB)诱导的CYP2B1和CYP2B2(CYP2B1/2B2)基因表达的影响。发现胰岛素、表皮生长因子、白细胞介素6、环磷酸腺苷(cAMP)、佛波醇12-肉豆蔻酸酯13-乙酸酯、肿瘤坏死因子α、钒酸盐和冈田酸在mRNA和蛋白质水平上抑制肝细胞中CYP2B1/2B2的诱导。cAMP和钒酸盐完全抑制大鼠肝细胞和肝脏中CYP2B1/2B2基因表达的诱导。向钒酸盐处理的肝细胞中添加染料木黄酮可部分恢复PB对CYP2B1/2B1基因表达的诱导。本研究的这些结果表明,磷酸化/去磷酸化步骤对于PB诱导CYP2B1/2B2基因表达至关重要。