Choi S W, Baek M Y, Kang M S
Department of Molecular Biology, College of Natural Science, Seoul National University, Korea.
Exp Cell Res. 1992 Mar;199(1):129-33. doi: 10.1016/0014-4827(92)90470-s.
We found that a transient rise in cGMP levels, which was closely associated with the Ca2+ influx, occurred concomitant with the onset of myoblast fusion. The Ca2+ channel blocker D600 decreased both the cell fusion and the normal rise in cGMP levels. In contrast, the Ca2+ ionophore A23187 transiently increased cGMP levels and induced precocious fusion. In addition, the cGMP analog 8-Br-cGMP induced precocious fusion as A23187 did. The guanylate cyclase inhibitor, methylene blue delayed the fusion in a dose-dependent manner without significantly affecting cell alignment, proliferation, or muscle-specific protein expression. Furthermore, methylene blue delayed the normal rise in cGMP levels, and the fusion block imposed by methylene blue was significantly recovered by 8-Br-cGMP. On the basis of our present findings, we suggest that a Ca2+ influx-dependent rise in cGMP levels is an important step in myoblast fusion.
我们发现,伴随着成肌细胞融合的开始,会出现cGMP水平的短暂升高,这与Ca2+内流密切相关。Ca2+通道阻滞剂D600可降低细胞融合以及cGMP水平的正常升高。相反,Ca2+离子载体A23187可使cGMP水平短暂升高并诱导早熟融合。此外,cGMP类似物8-Br-cGMP与A23187一样可诱导早熟融合。鸟苷酸环化酶抑制剂亚甲蓝以剂量依赖的方式延迟融合,而对细胞排列、增殖或肌肉特异性蛋白表达无明显影响。此外,亚甲蓝延迟了cGMP水平的正常升高,8-Br-cGMP可显著恢复亚甲蓝所造成的融合阻滞。基于我们目前的研究结果,我们认为cGMP水平依赖于Ca2+内流的升高是成肌细胞融合的重要步骤。