Wayne S, Jamieson J C, Spearman M A, Wright J A
Department of Chemistry, University of Manitoba, Winnipeg, Canada.
Mol Cell Biochem. 1990 Feb 9;92(2):137-46. doi: 10.1007/BF00218131.
The effect of ketoconazole on the fusion of L6 myoblasts was studied. Ketoconazole was a potent inhibitor of myoblast fusion at concentrations as low as 0.1 microM, but fusion was restored when the inhibitor was removed. The inhibitor resulted in decreased binding of conA and WGA to cell surface oligosaccharides showing that it was inhibiting N-linked cell surface glycoproteins. Inhibition of fusion by ketoconazole was accompanied by reduced creatine phosphokinase activities showing that it is affecting biochemical differentiation. Incorporation of labelled mannose from GDP-mannose into lipid-sugar and lipid-oligosaccharide complexes involved in the synthesis of N-linked oligosaccharides was also inhibited by ketoconazole, but the inhibition was reversed by addition of exogenous dolichol phosphate to the incorporation mixture. The main conclusion from these studies was that ketoconazole inhibited fusion of L6 myoblasts by affecting the synthesis of dolichol-phosphate required for the synthesis of lipid-oligosaccharides needed for the synthesis of fusogenic cell surface N-linked glycoproteins.
研究了酮康唑对L6成肌细胞融合的影响。酮康唑在低至0.1微摩尔浓度时就是成肌细胞融合的有效抑制剂,但去除抑制剂后融合得以恢复。该抑制剂导致伴刀豆球蛋白A(conA)和麦胚凝集素(WGA)与细胞表面寡糖的结合减少,表明它在抑制N-连接的细胞表面糖蛋白。酮康唑对融合的抑制伴随着肌酸磷酸激酶活性降低,表明它正在影响生化分化。酮康唑也抑制了将GDP-甘露糖中的标记甘露糖掺入参与N-连接寡糖合成的脂糖和脂寡糖复合物中,但通过向掺入混合物中添加外源性磷酸多萜醇可逆转这种抑制作用。这些研究的主要结论是,酮康唑通过影响合成融合性细胞表面N-连接糖蛋白所需的脂寡糖所必需的磷酸多萜醇的合成,从而抑制L6成肌细胞的融合。