Hazelton B J, Tupper J T
Biochem J. 1981 Mar 15;194(3):707-11. doi: 10.1042/bj1940707.
The lowering of extracellular Ca2+ concentration in the growth medium reversibly blocks normal, but not SV40-transformed WI38 diploid fibroblasts in the early G1/G0 phase of the cell cycle. This growth response is characterized by specific changes in ionic content and transport. Ca2+ deprivation (0.03 mM) has little effect on the K+ content of either normal or transformed cells. Na+ content, however, is increased nearly 2-fold in the normal cells. This increase is presumably due to a 3-fold increase in unidirectional Na+ influx in Ca2+-deprived cells. The increased intracellular Na+ also gives rise to a nearly 3-fold enhancement of the active (ouabain-sensitive) Na+ efflux. Ca2+ deprivation causes only slight increases in Na+ influx, ouabain-sensitive Na+ efflux and intracellular Na+ in the transformed cell. In contrast, the transformed cells lose nearly 60% of their intracellular Ca2+ on deprivation, whereas normal WI38 cells lose only 10%. The data suggest that the growth arrest exhibited by the normal cell but not the transformed cell may be related to different membrane-transport and permeability changes in response to Ca2+ deprivation.
生长培养基中细胞外Ca2+浓度的降低可逆地阻断处于细胞周期早期G1/G0期的正常WI38二倍体成纤维细胞,但不阻断SV40转化的WI38二倍体成纤维细胞。这种生长反应的特征是离子含量和转运的特定变化。Ca2+剥夺(0.03 mM)对正常细胞或转化细胞的K+含量影响很小。然而,正常细胞中的Na+含量增加了近2倍。这种增加可能是由于Ca2+剥夺细胞中单向Na+内流增加了3倍。细胞内Na+的增加还导致活性(哇巴因敏感)Na+外流增加了近3倍。Ca2+剥夺仅使转化细胞中的Na+内流、哇巴因敏感的Na+外流和细胞内Na+略有增加。相反,剥夺时转化细胞失去了近60%的细胞内Ca2+,而正常WI38细胞仅失去10%。数据表明,正常细胞而非转化细胞表现出的生长停滞可能与对Ca2+剥夺的不同膜转运和通透性变化有关。