TY - JOUR
T1 - Possible involvement of GTP-Binding proteins in 1α,25-Dihydroxyvitamin D3 induction of tissue transglutaminase in mouse peritoneal macrophages
AU - Ishii, Isao
AU - Ui, Michio
PY - 1994/9/30
Y1 - 1994/9/30
N2 - 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 1α,25-dihydroxyvitamin D3 (1α,25-(OH)2D3) or retinoic acid but not by steroid hormones. The induction by 1α,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 1α,25-(OH)2D3-induced enzyme gene expression.
AB - 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 1α,25-dihydroxyvitamin D3 (1α,25-(OH)2D3) or retinoic acid but not by steroid hormones. The induction by 1α,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 1α,25-(OH)2D3-induced enzyme gene expression.
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U2 - 10.1006/bbrc.1994.2392
DO - 10.1006/bbrc.1994.2392
M3 - Article
C2 - 7945328
AN - SCOPUS:0028125024
SN - 0006-291X
VL - 203
SP - 1773
EP - 1780
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -