Hoffman P C, Richman C M, Hsu R C, Chung J, Scanu A M, Yachnin S
Blood. 1981 Jan;57(1):164-9.
Oxygenated sterol compounds are potent inhibitors of sterol and DNA synthesis in mammalian cells. We studied the effects of oxygenated sterols on human marrow granulocytic progenitor cells in vitro (CFU-C). 25-Hydroxycholesterol was found to be a potent inhibitor of sterol synthesis in marrow mononuclear cells, with 50% inhibition occurring at approximately 10(-7) M. This compound, as well as 6-ketocholestanol, 7-ketocholesterol, and 20 alpha-hydroxycholesterol, also demonstrated marked inhibition of CFU-C proliferation. The latter effect, which was not a result of direct cytoxicity of the compounds, was reversible by cholesterol, but not by mevalonic acid. We conclude that inhibition of sterol synthesis by oxygenated sterol compounds may be insufficient to explain their suppression of CFU-C proliferation.
氧化甾醇化合物是哺乳动物细胞中甾醇和DNA合成的有效抑制剂。我们在体外研究了氧化甾醇对人骨髓粒细胞祖细胞(CFU-C)的影响。发现25-羟基胆固醇是骨髓单个核细胞中甾醇合成的有效抑制剂,在约10^(-7) M时出现50%的抑制。该化合物以及6-酮胆甾烷醇、7-酮胆固醇和20α-羟基胆固醇也表现出对CFU-C增殖的显著抑制。后一种效应不是化合物直接细胞毒性的结果,可被胆固醇逆转,但不能被甲羟戊酸逆转。我们得出结论,氧化甾醇化合物对甾醇合成的抑制可能不足以解释它们对CFU-C增殖的抑制作用。