Welham M J, Schrader J W
Biomedical Research Centre, University of British Columbia, Vancouver, Canada.
Mol Cell Biol. 1991 May;11(5):2901-4. doi: 10.1128/mcb.11.5.2901-2904.1991.
We examined the effects of various hemopoietins on c-kit mRNA and protein expression. Interleukin-3 (IL-3), granulocyte-macrophage colony-stimulating factor, and erythropoietin, but not IL-4, down-regulated levels of c-kit mRNA expressed by mast cells and stem cell progenitors. The effect of IL-3 was dominant and independent of cell growth or viability and was paralleled by reduced expression in c-kit protein. These observations indicate that regulation of c-kit expression is closely interlinked with the molecular mechanisms triggered by erythropoietin, IL-3, and granulocyte-macrophage colony-stimulating factor.
我们研究了各种造血生长因子对c-kit信使核糖核酸(mRNA)和蛋白质表达的影响。白细胞介素-3(IL-3)、粒细胞-巨噬细胞集落刺激因子和促红细胞生成素可下调肥大细胞和干细胞祖细胞表达的c-kit mRNA水平,但IL-4无此作用。IL-3的作用占主导地位,且与细胞生长或活力无关,同时c-kit蛋白表达也相应降低。这些观察结果表明,c-kit表达的调控与促红细胞生成素、IL-3和粒细胞-巨噬细胞集落刺激因子触发的分子机制密切相关。