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HeLa细胞中两种调节碱金属阳离子机制的相互作用。

Interaction of two mechanisms regulating alkali cations in HeLa cells.

作者信息

Cook J S, Vaughan G L, Proctor W R, Brake E T

出版信息

J Cell Physiol. 1975 Aug;86(1):59-70. doi: 10.1002/jcp.1040860108.

DOI:10.1002/jcp.1040860108
PMID:1176541
Abstract

The alkali cation content of HeLa cells is independent of culture density and of whether the cells are grown in suspension or attached to the culture vessel. With a cell doubling time of 28 hours, the cell K content turns over approximately once per hour. Following partial blockade of the alkali-cation transport system with ouabain, two distinct but interrelated mechanisms operate in the cellular response: (a) an increase in intracellular Na stimulates the pump so that the short-term alteration in electrolyte compostition is less than would be expected from the fraction of pump sites inhibited, and (b) there is a cycloheximide-sensitive recovery in transport capacity reflecting a restoration of functional transport sites to their normal density on the cell surface. Experimental manipulations that mimic the effect of ouabain lead to a stimulation of transport, but they do not result in an increase in the number of ouabain-binding sites on the surface. The data are consistent with a four-to-six hour turn-over of transport sites at the surface, but there is no evidence for a speicific induction of the transport system within this short-term recovery period.

摘要

HeLa细胞中的碱金属阳离子含量与培养密度无关,也与细胞是悬浮生长还是贴壁生长在培养容器上无关。细胞倍增时间为28小时,细胞内钾含量大约每小时更新一次。在用哇巴因部分阻断碱金属阳离子转运系统后,细胞反应中有两种不同但相互关联的机制在起作用:(a) 细胞内钠的增加刺激了泵,因此电解质组成的短期变化小于根据被抑制的泵位点比例所预期的变化;(b) 转运能力有对放线菌酮敏感的恢复,这反映了功能性转运位点在细胞表面恢复到其正常密度。模拟哇巴因作用的实验操作会导致转运的刺激,但不会导致表面哇巴因结合位点数量的增加。数据与表面转运位点四到六小时的更新一致,但没有证据表明在这个短期恢复期内转运系统有特异性诱导。

相似文献

1
Interaction of two mechanisms regulating alkali cations in HeLa cells.HeLa细胞中两种调节碱金属阳离子机制的相互作用。
J Cell Physiol. 1975 Aug;86(1):59-70. doi: 10.1002/jcp.1040860108.
2
[Dependence of ion transport across the plasma membrane on cell culture density. II. Active and passive cation transport during the growth of L cell cultures].[离子跨质膜运输对细胞培养密度的依赖性。II. L细胞培养生长过程中的主动和被动阳离子运输]
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Vasopressin rapidly stimulates Na entry and Na-K pump activity in quiescent cultures of mouse 3T3 cells.血管加压素能迅速刺激静止状态的小鼠3T3细胞培养物中的钠离子内流和钠钾泵活性。
J Cell Physiol. 1980 Oct;105(1):153-62. doi: 10.1002/jcp.1041050117.

引用本文的文献

1
Intracellular univalent cations and the regulation of the BALB/c-3T3 cell cycle.细胞内单价阳离子与BALB/c - 3T3细胞周期的调控
J Cell Biol. 1981 Jan;88(1):51-6. doi: 10.1083/jcb.88.1.51.
2
Mechanism and role of furosemide-sensitive K+ transport in L cells: a genetic approach.呋塞米敏感的钾离子转运在L细胞中的机制及作用:一种遗传学方法
J Membr Biol. 1980;52(3):245-56. doi: 10.1007/BF01869193.
3
Single channel K+ currents from HeLa cells.来自HeLa细胞的单通道钾离子电流。
J Membr Biol. 1983;74(1):41-9. doi: 10.1007/BF01870593.
4
Amplification of sodium- and potassium-activated adenosinetriphosphatase in HeLa cells by ouabain step selection.通过哇巴因逐步筛选法对HeLa细胞中钠钾激活的三磷酸腺苷酶进行扩增。
J Cell Biol. 1984 Sep;99(3):971-83. doi: 10.1083/jcb.99.3.971.
5
Ion concentration-dependent regulation of Na,K-pump abundance.钠钾泵丰度的离子浓度依赖性调节。
J Membr Biol. 1988 Nov;105(3):187-95. doi: 10.1007/BF01870996.
6
Serum stimulates the Na+,K+ pump in quiescent fibroblasts by increasing Na+ entry.血清通过增加钠离子内流来刺激静止成纤维细胞中的钠钾泵。
Proc Natl Acad Sci U S A. 1978 Nov;75(11):5560-4. doi: 10.1073/pnas.75.11.5560.