Ponomarchuk Olga, Boudreault Francis, Orlov Sergei N, Grygorczyk Ryszard
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.
Pflugers Arch. 2016 Nov;468(11-12):2075-2085. doi: 10.1007/s00424-016-1896-4. Epub 2016 Oct 31.
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.
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。