Shimamura M, Urabe A, Takaku F, Mizuno M
Exp Hematol. 1986 Sep;14(8):766-70.
We have reported that the exogenous addition of dolichyl phosphate (Dol-P) enhances the colony-forming capacities of early erythroid progenitors (BFU-E), late erythroid progenitors (CFU-E), and granulocyte-macrophage progenitors (CFU-GM) in adult mouse bone marrow, and that dolichol (Dol) enhances that of only CFU-E (Int. J. Cell Cloning 3:313, 1985). Compactin (2.5-10 microM), a specific inhibitor of mevalonate biosynthesis that causes a decrease of endogenous Dol biosynthesis, inhibited colony formation of CFU-GM. Exogenous addition of Dol-P partially prevented this inhibition, but Dol and the other mevalonate metabolites, such as cholesterol, coenzyme Q10, and isopentenyladenine, could not. In addition, we have found that the colony-forming capacity of CFU-E in fetal mouse liver was not enhanced by exogenous Dol or Dol-P. But the decrease of colony formation or DNA synthesis of fetal CFU-E in the presence of compactin was prevented by the exogenous addition of Dol or Dol-P.
我们曾报道,外源添加磷酸多萜醇(Dol-P)可增强成年小鼠骨髓中早期红系祖细胞(BFU-E)、晚期红系祖细胞(CFU-E)和粒-巨噬系祖细胞(CFU-GM)的集落形成能力,而多萜醇(Dol)仅增强CFU-E的集落形成能力(《国际细胞克隆杂志》3:313,1985年)。美伐他汀生物合成的特异性抑制剂康帕丁(2.5 - 10 microM)可导致内源性Dol生物合成减少,并抑制CFU-GM的集落形成。外源添加Dol-P可部分阻止这种抑制作用,但Dol以及其他美伐他汀代谢产物,如胆固醇、辅酶Q10和异戊烯腺嘌呤则不能。此外,我们发现外源Dol或Dol-P不能增强胎鼠肝脏中CFU-E的集落形成能力。但在外源添加Dol或Dol-P时,康帕丁存在下胎鼠CFU-E的集落形成或DNA合成的减少可被阻止。