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在没有细胞外钾的情况下,人红细胞钠钾泵磷酸化中间体(EP)中的磷酸盐与钠协同流出。

Phosphate from the phosphointermediate (EP) of the human red blood cell Na/K pump is coeffluxed with Na, in the absence of external K.

作者信息

Marín R, Hoffman J F

机构信息

Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

J Gen Physiol. 1994 Jul;104(1):1-32. doi: 10.1085/jgp.104.1.1.

Abstract

This study is concerned with Na/K pump-mediated phosphate efflux that occurs during uncoupled Na efflux in human red blood cells. Uncoupled Na efflux is known to be a ouabain-sensitive mode of the Na/K pump that occurs in the absence of external Nao and Ko. Because this efflux (measured with 22Na) is also inhibited by 5 mM Nao, the efflux can be separated into a Nao-sensitive and a Nao-insensitive component. Previous work established that the Nao-sensitive efflux is actually comprised of an electroneutral coefflux of Na with cellular anions, such as SO4 (as 35SO4). The present work focuses on the Nao-insensitive component in which the principal finding is that orthophosphate (P(i)) is coeffluxed with Na in a ouabain-sensitive manner. This P(i) efflux can be seen to occur, in the absence of Ko, in both DIDS-treated intact cells and resealed red cell ghosts. This efflux of P(i) was shown to be derived directly from the pump's substrate, ATP, by the use of resealed ghosts made to contain both ATP and P(i) in which either the ATP or the P(i) were labeled with, respectively, [gamma-32P]ATP or [32P]H3PO4. (These resealed ghosts also contained Na, Mg, P(i), SO4, Ap5A, as well as an arginine kinase/creatine kinase nucleotide regenerating system for the control of ATP and ADP concentrations, and were suspended usually in (NMG)2SO4 at pH 7.4.) It was found that 32P was only coeffluxed with Na when the 32P was contained in [gamma-32P]ATP and not in [32P]H3PO4. This result implies that the 32P that is released comes from ATP via the pump's phosphointermediate (EP) without commingling with the cellular pool of P(i). Ko (as K2SO4) inhibits this 32P efflux as well as the Nao-sensitive 35SO4 efflux, with a K0.5 of 0.3-0.4 mM. The K0.5 for inhibition of P(i) efflux by Ko is not influenced by Nao, nor can Nao act as a congenor for Ko in any of the flux reactions involving Ko. The stoichiometry of Na to SO4 and Na to P(i) efflux is approximately 2:1 under circumstances where the stoichiometry of Na effluxed to ATP utilized is 3:1. From these and other results reported, it is suggested that there are two types of uncoupled Na efflux that differ from each other on the basis of their sensitivity to Nao, the source (cellular vs substrate) and kind of anion (SO4 vs P(i)) transported.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本研究关注的是在人红细胞非偶联钠外流过程中由钠钾泵介导的磷酸盐外流。已知非偶联钠外流是钠钾泵的一种哇巴因敏感模式,它在没有外部钠离子(Nao)和钾离子(Ko)的情况下发生。由于这种外流(用22Na测量)也受到5 mM Nao的抑制,所以该外流可分为对Nao敏感和不敏感的成分。先前的研究表明,对Nao敏感的外流实际上是由钠与细胞内阴离子(如硫酸根(以35SO4形式))的电中性协同外流组成。目前的研究聚焦于对Nao不敏感的成分,其主要发现是正磷酸盐(P(i))以哇巴因敏感的方式与钠协同外流。在没有Ko的情况下,这种P(i)外流在二异丙基氟磷酸(DIDS)处理的完整细胞和重封的红细胞血影中均可观察到。通过使用含有ATP和P(i)的重封血影,其中ATP或P(i)分别用[γ-32P]ATP或[32P]H3PO4标记,结果表明这种P(i)外流直接来源于泵的底物ATP。(这些重封血影还含有钠、镁、P(i)、硫酸根、二磷酸五腺苷(Ap5A),以及用于控制ATP和二磷酸腺苷(ADP)浓度的精氨酸激酶/肌酸激酶核苷酸再生系统,并且通常悬浮在pH 7.4的硫酸(NMG)2溶液中。)发现只有当32P包含在[γ-32P]ATP中而非[32P]H3PO4中时,32P才与钠协同外流。这一结果表明,释放的32P来自于通过泵的磷酸中间体(EP)的ATP,而不与细胞内的P(i)池混合。Ko(以硫酸钾(K2SO4)形式)抑制这种32P外流以及对Nao敏感的35SO4外流,其半数抑制浓度(K0.5)为0.3 - 0.4 mM。Ko对P(i)外流的抑制的K0.5不受Nao影响,在任何涉及Ko的通量反应中,Nao也不能作为Ko的同类物起作用。在流出的钠与消耗的ATP的化学计量比为3:1的情况下,钠与硫酸根以及钠与P(i)外流的化学计量比约为2:1。根据这些及其他报道的结果,提示存在两种不同类型的非偶联钠外流,它们在对Nao的敏感性、阴离子的来源(细胞内与底物)以及所转运阴离子的种类(硫酸根与P(i))方面存在差异。(摘要截选至400字)

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