Ha R, Steenbergen D K, Kempson S A
Department of Physiology and Biophysics, Indiana University School of Medicine, Indianapolis 46202-5120.
Cell Biochem Funct. 1993 Jun;11(2):119-24. doi: 10.1002/cbf.290110207.
The rat osteosarcoma cell line UMR-106-01 has an osteoblast-like phenotype. When grown in monolayer culture these cells transport inorganic phosphate and L-alanine via Na(+)-dependent transport systems. Exposure of these cells to a low phosphate medium for 4 h produced a 60-70 per cent increase in Na(+)-dependent phosphate uptake compared to control cells maintained in medium with a normal phosphate concentration. In contrast, Na(+)-dependent alanine uptake and Na(+)-independent phosphate uptake were not changed during phosphate deprivation. The increased phosphate uptake was due, in part, to an increased Vmax and was blocked completely by pretreatment with cycloheximide (70 microM). In these cells recovery of intracellular pH after acidification with NH4Cl is due primarily to the Na+/H+ exchange system. The rate of this recovery process, monitored with a pH sensitive indicator (BCECF), was decreased by more than 50 per cent in phosphate-deprived cells compared to controls indicating that Na+/H+ exchange was inhibited during phosphate deprivation.
大鼠骨肉瘤细胞系UMR-106-01具有成骨细胞样表型。当在单层培养中生长时,这些细胞通过Na⁺依赖性转运系统转运无机磷酸盐和L-丙氨酸。与维持在正常磷酸盐浓度培养基中的对照细胞相比,将这些细胞暴露于低磷酸盐培养基4小时后,Na⁺依赖性磷酸盐摄取增加了60%-70%。相反,在磷酸盐缺乏期间,Na⁺依赖性丙氨酸摄取和Na⁺非依赖性磷酸盐摄取没有变化。磷酸盐摄取增加部分归因于Vmax增加,并且完全被环己酰亚胺(70微摩尔)预处理所阻断。在这些细胞中,用NH₄Cl酸化后细胞内pH的恢复主要归因于Na⁺/H⁺交换系统。与对照相比,在磷酸盐缺乏的细胞中,用pH敏感指示剂(BCECF)监测的这种恢复过程的速率降低了50%以上,这表明在磷酸盐缺乏期间Na⁺/H⁺交换受到抑制。