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鉴定人眼角膜内皮细胞中的瞬时受体电位香草醛通道 4(TRPV4)。

Characterization of transient receptor potential vanilloid channel 4 (TRPV4) in human corneal endothelial cells.

机构信息

Charité - Universitätsmedizin Berlin, Campus Virchow-Clinic, Department of Ophthalmology, Augustenburger Platz 1, 13353 Berlin, Germany.

出版信息

Exp Eye Res. 2011 Nov;93(5):710-9. doi: 10.1016/j.exer.2011.09.021. Epub 2011 Oct 6.

Abstract

The transient receptor potential vanilloid 4 (TRPV4) is a Ca(2+)-and Mg(2+) permeable cation channel that might be a cellular osmosensor since it is activated upon hypotonic cell swelling. TRPV4 is also thermosensitive and responds to moderate heat (from 24 to 27 °C) as well as to phorbol esters (4α-PDD) and several endogenous substances including arachidonic acid (AA), the endocannabinoids anandamide and 2-AG, and cytochrome P-450 metabolites of AA, such as epoxyeicosatrienoic acids. The resulting Ca(2+) influx occurring in response to swelling induces regulatory volume decrease (RVD) behavior. As regulation of cell volume is essential for corneal endothelial function, we determined whether human corneal endothelial cells have functional TRPV4 channel activity. RT-PCR identified TRPV4 gene expression in the HCEC-12 cell line as well as two clonal daughter cell lines (HCEC-H9C1, HCEC-B4G12). Ca(2+) transients were monitored in fura-2 loaded cells. Nonselective cation channel currents were recorded in the whole-cell mode of the planar patch-clamp technique. TRPV4 mRNA was found in HCEC-12 and the clonal daughter cell lines. TRPV4 channel agonists (4α-PDD and GSK1016790A; both 5 μmol/l) as well as moderate heat (<40 °C) elicited Ca(2+) transients. Hypotonicity increased Ca(2+) and nonselective cation channel currents in HCEC-12 cells. There is functional TRPV4 expression in HCEC-12 and in its clonal daughter cell lines based on Ca(2+) transients and underlying currents induced by known activators of this channel.

摘要

瞬时受体电位香草酸 4 型(TRPV4)是一种 Ca2+和 Mg2+通透性阳离子通道,它可能是一种细胞渗透压感受器,因为它在细胞肿胀时被激活。TRPV4 也对热敏感,对中等温度(24 至 27°C)以及佛波酯(4α-PDD)和几种内源性物质(包括花生四烯酸(AA)、内源性大麻素大麻素酸和 2-花生四烯酸甘油二酯以及 AA 的细胞色素 P-450 代谢物,如环氧二十碳三烯酸)有反应。肿胀引起的 Ca2+内流会引起调节性体积减少(RVD)行为。由于细胞体积的调节对于角膜内皮功能至关重要,因此我们确定人角膜内皮细胞是否具有功能性 TRPV4 通道活性。RT-PCR 在 HCEC-12 细胞系以及两个克隆子系(HCEC-H9C1、HCEC-B4G12)中鉴定出 TRPV4 基因表达。在负载 fura-2 的细胞中监测[Ca2+]i 瞬变。在平面膜片钳技术的全细胞模式下记录非选择性阳离子通道电流。在 HCEC-12 和克隆子系中均发现 TRPV4 mRNA。TRPV4 通道激动剂(4α-PDD 和 GSK1016790A;均为 5 μmol/l)以及中等温度(<40°C)均可引起[Ca2+]i 瞬变。低渗性增加 HCEC-12 细胞中的[Ca2+]i 和非选择性阳离子通道电流。基于已知该通道激活剂引起的 Ca2+瞬变和基础电流,在 HCEC-12 和其克隆子系中存在功能性 TRPV4 表达。

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