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低细胞外钾浓度对爱泼斯坦-巴尔病毒转化的人淋巴细胞系中Na+/K+泵数量和活性影响的逆转

Reversal of the effects of a low extracellular potassium concentration on the number and activity of Na+/K+ pumps in an Epstein-Barr virus-transformed human lymphocyte cell line.

作者信息

Ameen M, Bloomfield J G, Aronson J K

机构信息

MRC Unit, Radcliffe Infirmary, Oxford, U.K.

出版信息

Biochem Pharmacol. 1992 Feb 4;43(3):489-96. doi: 10.1016/0006-2952(92)90568-4.

Abstract

A reduction in the extracellular concentration of potassium to 0.5 mM (low K) in Epstein-Barr (EB) virus-transformed lymphocytes caused changes in the number and activity of Na+/K+ pumps in the cell membrane, with increases in the Bmax and apparent Kd of ouabain binding, and concomitant increases in the Vmax and apparent Km of potassium (rubidium) influx. However, recovery from the effects of low K occurred more quickly than the original up-regulation. Furthermore, there were differences in the time-courses of the separate rates of recovery of the Bmax and Kd of ouabain binding after the cells were returned to normal K, the rate of recovery of the Kd being quicker than that of the Bmax, which was biphasic, with slow and fast rates of recovery. Inhibition of protein synthesis by emetine caused an increase in the rate of recovery of the Bmax of ouabain binding, but no effect on the Kd, suggesting that the slow phase of recovery of the Bmax is attributable to the synthesis and insertion of new protein, while the rapid phase of recovery is independent of protein synthesis and may represent internalization. The results suggested that during up-regulation of pump number in response to low K about 40% of the newly inserted Na+/K+ pumps are normal and the rest are abnormal. The half-time of removal of the abnormal pumps from the cell membrane during recovery from low K stress was 2.8 hr and the half-time of internalization of the normal pumps was 4.3 hr.

摘要

将爱泼斯坦 - 巴尔(EB)病毒转化的淋巴细胞外钾浓度降至0.5 mM(低钾)会导致细胞膜中Na⁺/K⁺泵数量和活性发生变化,哇巴因结合的Bmax和表观Kd增加,同时钾(铷)内流的Vmax和表观Km也增加。然而,从低钾影响中恢复的速度比最初的上调更快。此外,细胞恢复到正常钾浓度后,哇巴因结合的Bmax和Kd的单独恢复速率的时间进程存在差异,Kd的恢复速率比双相的Bmax快,Bmax的恢复速率有慢有快。放线菌酮抑制蛋白质合成会导致哇巴因结合的Bmax恢复速率增加,但对Kd没有影响,这表明Bmax恢复的慢相归因于新蛋白质的合成和插入,而快速恢复相独立于蛋白质合成,可能代表内化。结果表明,在对低钾反应中泵数量上调期间,新插入的Na⁺/K⁺泵约40%是正常的,其余是异常的。从低钾应激恢复过程中,异常泵从细胞膜上移除的半衰期为2.8小时,正常泵内化的半衰期为4.3小时。

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