Taoka T, Itano T, Tokuda M, Tanaka T, Hatase O, Irino S
First Department of Internal Medicine, Kagawa Medical School, Japan.
Biochem Int. 1989 Jun;18(6):1193-201.
The roles of calcium (Ca2+) and protein kinase C in the differentiation of HL-60 cells induced by 1 alpha,25(OH)2D3 (D3) and/or a Ca2+ antagonist, diltiazem(D-cis, L-cis), were elucidated. D3 and diltiazem (100 microM) inhibited cell proliferation, and diltiazem enhanced the D3-induced differentiation. There was no difference in potency between the two isomers of diltiazem in the enhancing activity, in spite of their different pharmacological activity. The concentration of free Ca2+ in the HL-60 cells following D3 and/or diltiazem treatment significantly increased. A protein kinase C inhibitor, H-7, inhibited the phenotypic differentiation induced by D3. These results suggest that Ca2+ and protein kinase C play an important role in the differentiation of HL-60 cells induced by D3 and diltiazem.
研究了钙(Ca2+)和蛋白激酶C在1α,25(OH)2D3(D3)和/或钙拮抗剂地尔硫卓(D-顺式,L-顺式)诱导的HL-60细胞分化中的作用。D3和地尔硫卓(100微摩尔)抑制细胞增殖,且地尔硫卓增强了D3诱导的分化。尽管地尔硫卓的两种异构体具有不同的药理活性,但其增强活性的效力并无差异。用D3和/或地尔硫卓处理后,HL-60细胞中的游离Ca2+浓度显著增加。蛋白激酶C抑制剂H-7抑制了D3诱导的表型分化。这些结果表明,Ca2+和蛋白激酶C在D3和地尔硫卓诱导的HL-60细胞分化中起重要作用。