Suppr超能文献

铵依赖性钠摄取在斑马鱼(Oryzias latipes)幼虫的富含线粒体的细胞中。

Ammonium-dependent sodium uptake in mitochondrion-rich cells of medaka (Oryzias latipes) larvae.

机构信息

Department of Life Science, National Taiwan Normal University, Taipei 116, Taiwan, ROC.

出版信息

Am J Physiol Cell Physiol. 2010 Feb;298(2):C237-50. doi: 10.1152/ajpcell.00373.2009. Epub 2009 Nov 25.

Abstract

In this study, a scanning ion-selective electrode technique (SIET) was applied to measure H(+), Na(+), and NH(4)(+) gradients and apparent fluxes at specific cells on the skin of medaka larvae. Na(+) uptake and NH(3)/NH(4)(+) excretion were detected at most mitochondrion-rich cells (MRCs). H(+) probing at MRCs revealed two group of MRCs, i.e., acid-secreting and base-secreting MRCs. Treatment with EIPA (100 muM) blocked 35% of the NH(3)/NH(4)(+) secretion and 54% of the Na(+) uptake, suggesting that the Na(+)/H(+) exchanger (NHE) is involved in Na(+) and NH(3)/NH(4)(+) transport. Low-Na(+) water (<0.001 mM) or high-NH(4)(+) (5 mM) acclimation simultaneously increased Na(+) uptake and NH(3)/NH(4)(+) excretion but decreased or even reversed the H(+) gradient at the skin and MRCs. The correlation between NH(4)(+) production and H(+) consumption at the skin surface suggests that MRCs excrete nonionic NH(3) (base) by an acid-trapping mechanism. Raising the external NH(4)(+) significantly blocked NH(3)/NH(4)(+) excretion and Na(+) uptake. In contrast, raising the acidity of the water (pH 7 to pH 6) enhanced NH(3)/NH(4)(+) excretion and Na(+) uptake by MRCs. In situ hybridization and real-time PCR showed that the mRNAs of the Na(+)/H(+) exchanger (slc9a3) and Rhesus glycoproteins (Rhcg1 and Rhbg) were colocalized in MRCs of medaka, and their expressions were induced by low-Na(+) acclimation. This study suggests a novel Na(+)/NH(4)(+) exchange pathway in apical membranes of MRCs, in which a coupled NHE and Rh glycoprotein is involved and the Rh glycoprotein may drive the NHE by generating H(+) gradients across apical membranes of MRCs.

摘要

在这项研究中,扫描离子选择性电极技术(SIET)被应用于测量斑马鱼幼虫皮肤特定细胞上的 H(+)、Na(+)和 NH(4)(+)梯度和表观通量。Na(+)的摄取和 NH(3)/NH(4)(+)的排泄在大多数富含线粒体的细胞(MRCs)中被检测到。在 MRCs 上进行的 H(+)探测揭示了两组 MRCs,即分泌酸的 MRCs 和分泌碱的 MRCs。用 EIPA(100 μM)处理可阻断 35%的 NH(3)/NH(4)(+)分泌和 54%的 Na(+)摄取,表明 Na(+)/H(+)交换器(NHE)参与了 Na(+)和 NH(3)/NH(4)(+)的转运。低 Na(+)水(<0.001 mM)或高 NH(4)(+)(5 mM)驯化同时增加了 Na(+)摄取和 NH(3)/NH(4)(+)的排泄,但降低了甚至逆转了皮肤和 MRCs 上的 H(+)梯度。皮肤表面 NH(4)(+)产生与 H(+)消耗之间的相关性表明,MRCs 通过酸捕获机制排泄非离子型 NH(3)(碱)。提高外源性 NH(4)(+)显著阻断了 NH(3)/NH(4)(+)的排泄和 Na(+)的摄取。相比之下,提高水的酸度(pH7 至 pH6)通过 MRCs 增强了 NH(3)/NH(4)(+)的排泄和 Na(+)的摄取。原位杂交和实时 PCR 显示,Na(+)/H(+)交换器(slc9a3)和 Rhus 糖蛋白(Rhcg1 和 Rhbg)的 mRNAs 在斑马鱼的 MRCs 中发生共定位,它们的表达在低 Na(+)驯化时被诱导。本研究表明,在 MRCs 的顶端膜上存在一种新的 Na(+)/NH(4)(+)交换途径,其中涉及耦合的 NHE 和 Rh 糖蛋白,并且 Rh 糖蛋白可能通过在 MRCs 的顶端膜上产生 H(+)梯度来驱动 NHE。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验