Ishii I, Ui M
Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1994 Sep 30;203(3):1773-80. doi: 10.1006/bbrc.1994.2392.
Induction of transglutaminase was analyzed based on increases in the maximal enzymic activity and in the Northern blots of mRNA during culture of mouse resident peritoneal macrophages with active forms of hydrophobic vitamins and steroid hormones. The enzyme was induced by 1 alpha,25-dihydroxyvitamin D3 (1 alpha,25-(OH)2D3) or retinoic acid but not by steroid hormones. The induction by 1 alpha,25-(OH)2D3 was characterized by its slow onset and marked synergism with retinoic acid induction. The induction was enhanced by protein kinase activators such as cholera toxin and phorbol 12-myristate 13-acetate but largely inhibited by pertussis toxin treatment of cells. It is suggested that pertussis toxin-linked and protein kinase-related signaling would mediate the 1 alpha,25-(OH)2D3-induced enzyme gene expression.
基于在小鼠常驻腹膜巨噬细胞与疏水维生素和类固醇激素的活性形式培养期间最大酶活性和mRNA的Northern印迹的增加,分析转谷氨酰胺酶的诱导情况。该酶由1α,25 - 二羟基维生素D3(1α,25-(OH)2D3)或视黄酸诱导,但不由类固醇激素诱导。1α,25-(OH)2D3的诱导其特点是起效缓慢且与视黄酸诱导有明显协同作用。蛋白激酶激活剂如霍乱毒素和佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯可增强诱导作用,但细胞经百日咳毒素处理后诱导作用大多受到抑制。提示百日咳毒素相关和蛋白激酶相关信号传导将介导1α,25-(OH)2D3诱导的酶基因表达。