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钠钾泵在肾单位中的表达与分布。

Na,K-pump expression and distribution in the nephron.

作者信息

Farman N

机构信息

INSERM U246, IFR, Cellules Epithéliales, Faculté de Médecine X. Bichat, Paris, France.

出版信息

Miner Electrolyte Metab. 1996;22(5-6):272-8.

PMID:8933498
Abstract

Na+,K(+)-ATPase plays a major role in the reabsorption of sodium by the kidney. This organ is highly heterogeneous, and its functional unit, the nephron, is formed of successive epithelia with specific morphological and functional characteristics. Na+,K(+)-ATPase expression varies along the nephron. Variations in the catalytic activity of the pump, the number of active pumps expressed in the basolateral membrane, its substrate dependency towards Na and K, and its sensitivity to the inhibitor ouabain have been observed in distinct tubular segments. Most authors agree on the large (or unique) prevalence of the alpha 1 and beta 1 isoforms of the two subunits of Na+,K(+)-ATPase in each nephron segment, although at different levels. The cortical collecting duct represents a unique epithelium to study the physiological relevance of the regulation of Na+,K(+)-ATPase activity, including an immediate substrate activation, a rapid recruitment of active pumps from a reserve pool, and long-term hormonal effects. Whether these functions require other molecular determinants than the alpha 1 and beta 1 isoform subunits remains to be established.

摘要

钠钾ATP酶在肾脏对钠的重吸收过程中起主要作用。肾脏具有高度的异质性,其功能单位肾单位由具有特定形态和功能特征的连续上皮细胞构成。钠钾ATP酶的表达沿肾单位各部分有所不同。在不同的肾小管节段中,已观察到该泵催化活性的变化、基底外侧膜上表达的活性泵数量、其对钠和钾的底物依赖性以及对抑制剂哇巴因的敏感性。尽管表达水平不同,但大多数作者一致认为,在每个肾单位节段中,钠钾ATP酶两个亚基的α1和β1同工型占主导(或唯一)地位。皮质集合管是研究钠钾ATP酶活性调节生理相关性的独特上皮组织,包括即时底物激活、从储备池中快速募集活性泵以及长期激素效应。这些功能是否需要除α1和β1同工型亚基之外的其他分子决定因素仍有待确定。

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引用本文的文献

1
Sodium-pump gene-expression, protein abundance and enzyme activity in isolated nephron segments of the aging rat kidney.衰老大鼠肾脏分离肾单位节段中钠泵基因表达、蛋白质丰度及酶活性
Physiol Rep. 2015 Jun;3(6). doi: 10.14814/phy2.12369.
2
Renovascular hypertension using a modified two-kidney, one-clip approach in mice is not dependent on the α1 or α2 Na-K-ATPase ouabain-binding site.采用改良的两肾一夹法在小鼠中建立的肾血管性高血压并不依赖于α1或α2 Na-K-ATP 酶哇巴因结合位点。
Am J Physiol Renal Physiol. 2011 Sep;301(3):F615-21. doi: 10.1152/ajprenal.00158.2011. Epub 2011 Jun 1.