Suppr超能文献

在低渗刺激的A549上皮细胞中,触发体积恢复不需要钙。

Calcium is not required for triggering volume restoration in hypotonically challenged A549 epithelial cells.

作者信息

Ponomarchuk Olga, Boudreault Francis, Orlov Sergei N, Grygorczyk Ryszard

机构信息

Centre de recherche, Centre hospitalier de l'Université de Montréal (CRCHUM), Tour Viger 900 rue St-Denis, Montreal, Quebec, H2X 0A9, Canada.

Faculty of Biology, M.V. Lomonosov Moscow State University, Moscow, Russia.

出版信息

Pflugers Arch. 2016 Nov;468(11-12):2075-2085. doi: 10.1007/s00424-016-1896-4. Epub 2016 Oct 31.

Abstract

Maintenance of cell volume is a fundamental housekeeping function in eukaryotic cells. Acute cell swelling activates a regulatory volume decrease (RVD) process with poorly defined volume sensing and intermediate signaling mechanisms. Here, we analyzed the putative role of Ca signaling in RVD in single substrate-adherent human lung epithelial A549 cells. Acute cell swelling was induced by perfusion of the flow-through imaging chamber with 50 % hypotonic solution at a defined fluid turnover rate. Changes in cytosolic Ca concentration ([Ca]) and cell volume were monitored simultaneously with ratiometric Fura-2 fluorescence and 3D reconstruction of stereoscopic single-cell images, respectively. Hypotonic challenge caused a progressive swelling peaking at ∼20 min and followed, during the next 20 min, by RVD of 60 ± 7 % of the peak volume increase. However, at the rate of swelling used in our experiments, these processes were not accompanied by a measurable increment of [Ca]. Loading with intracellular Ca chelator BAPTA slightly delayed peak of swelling but did not prevent RVD in 82 % of cells. Further, electrophysiology whole-cell patch-clamp experiments showed that BAPTA did not block activation of volume-regulated anion channel (VRAC) measured as swelling-induced outwardly rectifying 5-nitro-2-(3-phenylpropyl-amino) benzoic acid sensitive current. Together, our data suggest that intracellular Ca-mediated signaling is not essential for VRAC activation and subsequent volume restoration in A549 cells.

摘要

维持细胞体积是真核细胞的一项基本看家功能。急性细胞肿胀会激活调节性容积减小(RVD)过程,但其容积感应和中间信号传导机制尚不明确。在此,我们分析了钙信号在单底物贴壁的人肺上皮A549细胞RVD中的假定作用。通过以确定的液体周转率用50%的低渗溶液灌注流通成像室来诱导急性细胞肿胀。分别用比率型Fura-2荧光和立体单细胞图像的三维重建同时监测细胞溶质钙浓度([Ca])和细胞体积的变化。低渗刺激导致逐渐肿胀,在约20分钟时达到峰值,随后在接下来的20分钟内,RVD达到峰值体积增加的60±7%。然而,在我们实验中使用的肿胀速率下,这些过程并未伴随着[Ca]的可测量增加。用细胞内钙螯合剂BAPTA加载稍微延迟了肿胀峰值,但并未阻止82%的细胞发生RVD。此外,电生理全细胞膜片钳实验表明,BAPTA并未阻断作为肿胀诱导的外向整流5-硝基-2-(3-苯基丙基-氨基)苯甲酸敏感电流所测量的容积调节性阴离子通道(VRAC)的激活。总之,我们的数据表明,细胞内钙介导的信号传导对于A549细胞中VRAC的激活和随后的容积恢复并非必不可少。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验