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首页> 外文期刊>American Journal of Physiology >Combinatorial expression of claudins in the proximal renal tubule and its functional consequences.
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Combinatorial expression of claudins in the proximal renal tubule and its functional consequences.

机译:近端肾小管中克劳德林的组合表达及其功能后果。

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摘要

The proximal renal tubule (PT) is characterized by a highly conductive paracellular pathway, which contributes to a significant amount of solute and water reabsorption by the kidney. Claudins are tight junction proteins that, in part, determine the paracellular permeability of epithelia. In the present study, we determined the expression pattern of the major FT claudins. We found that claudin-2 and claudin-10 are coexpressed throughout the PT, whereas claudin-3 is coexpressed with claudin-2 predominantly in the proximal straight tubule. Additionally, claudin-2 and claudin-3 are expressed separately within mutually exclusive populations of descending thin limbs. We developed a novel double-inducible Madin-Darby canine kidney I cell model to characterize in vitro the functional effect of coexpression of PT claudins. In keeping with previous studies, we found that claudin-2 alone primarily increased cation (Na~+ and Ca~2+) permeability, whereas claudin-10a alone increased anion (Cl~-) permeability. Coexpression of claudin-2 and claudin-lOa together led to a weak physical interaction between the isoforms and the formation of a monolayer with high conductance but neutral charge selectivity. Claudin-3 expression had a negligible effect on all measures of cell permeability, whether expressed alone or together with claudin-2. In cells coexpressing a claudin-2 mutant, S68C, together with claudin-10a, inhibition of cation permeability through the claudin-2 pore with a thiol-reactive pore blocker did not block anion permeation through claudin-lOa. We conclude that claudin-2 and claudin-lOa form independent paracellular cation- and anion-selective channels that function in parallel.
机译:近端肾小管(Pt)的特征在于具有高导电锥虫途径,这有助于肾脏的大量溶质和水重吸收。 Claudins是紧密的接线蛋白,部分地确定上皮细胞间渗透性。在本研究中,我们确定了主要FT Claudins的表达模式。我们发现在整个PT中共同表达了ClaudIn-2和Claudin-10,而Claudin-3主要用克劳丁-2在近端直线管中与ClaudIn-2共表达。另外,Claudin-2和Claudin-3分别在降稀肢的相互排斥的群体中表达。我们开发了一种新型双重诱导的Madin-Darby犬肾I细胞模型,以表征体外Pt Claudins的共同抑制功能效果。为了与以前的研究保持一致,我们发现Claudin-2单独增加阳离子(Na〜+和Ca〜2 +)渗透性,而Claudin-10a单独增加阴离子(Cl〜 - )渗透性。 CLAUDIN-2和CLAUDIN-LOA的共表达导致同种型之间的弱物理相互作用和具有高导率但中性电荷选择性的单层形成单层。无论单独表达还是与克劳德蛋白-2,克劳丁素-3表达对所有细胞渗透性的措施都具有可忽略不计的影响。在将克劳德蛋白-2突变体的细胞中,S68C与Claudin-10a一起,通过Claudin-2孔用硫醇反应性孔阻断剂抑制阳离子渗透性并未通过Claudin-LoA阻断阴离子渗透。我们得出结论,ClaudIn-2和Claudin-LoA形成独立的肺状阳离子和阴离子选择性通道,该阳离子和阴离子选择性通道并联起作用。

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