Crowe R A, Taparowsky E J, Crane F L
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907-1392.
Biochem Biophys Res Commun. 1993 Oct 29;196(2):844-50. doi: 10.1006/bbrc.1993.2326.
The ras family of oncogenes, as well as the transplasma membrane electron transport system, have been implicated in cellular growth control. Here we present evidence that the Ha-ras oncoprotein increases the activity of the transplasma membrane electron transport system in the mouse embryonic fibroblast cell line C3H10T1/2. Both cytochrome c and ferricyanide are reduced at a faster rate by C3H10T1/2 cells which are expressing the Ha-ras oncogene. In addition, the Ha-ras transformed cells extrude protons faster in response to stimulation by external oxidants than their normal counterparts. These results suggest that transformation events initiated by the expression of the Ha-ras oncoprotein, p21, in C3H10T1/2 cells have a controlling effect on the transplasma membrane electron transport system.
癌基因的ras家族以及跨质膜电子传递系统与细胞生长控制有关。在此,我们提供证据表明,Ha-ras癌蛋白可增加小鼠胚胎成纤维细胞系C3H10T1/2中跨质膜电子传递系统的活性。表达Ha-ras癌基因的C3H10T1/2细胞能以更快的速率还原细胞色素c和铁氰化物。此外,Ha-ras转化细胞在受到外部氧化剂刺激时比正常细胞更快地排出质子。这些结果表明,在C3H10T1/2细胞中由Ha-ras癌蛋白p21的表达引发的转化事件对跨质膜电子传递系统具有控制作用。