Ohata H, Tanaka K, Maeyama N, Yamamoto M, Momose K
Department of Pharmacology, School of Pharmaceutical Sciences, Showa University, Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
J Physiol. 2001 Apr 1;532(Pt 1):31-42. doi: 10.1111/j.1469-7793.2001.0031g.x.
Local increases in the intracellular Ca2+ concentration ([Ca2+]i) in several regions within the bovine lens epithelial cell during application of mechanical stress were clearly visualized in the presence of lysophosphatidic acid (LPA), a bioactive lysophospholipid, using real-time confocal microscopy. We called the phenomenon 'Ca2+ spots'. Ca2+ spots started in a circular area with a radius of about 1.5 m. These Ca2+ spots spread concentrically, resulting in a mean global increase in [Ca2+]i. The local increase often occurred in a stepwise manner or repetitively at the same region. The spatiotemporal properties of the Ca2+ spots were completely different from those of the Ca2+ wave induced by ATP, a Ca2+-mobilizing agonist. Ca2+ spots were inhibited by decreasing the extracellular Ca2+ concentration or by the presence of Gd3+, an inhibitor of mechanosensitive (MS) channels, but not by thapsigargin, an inhibitor of the endoplasmic reticulum Ca2+ pump, suggesting that Ca2+ spots arise from Ca2+ influx through Gd3+-sensitive MS channels. On the assumption that, in lens epithelial cells, the open probability of the MS channel is 0.4, the membrane potential is 56 mV and the channel conductance is 50 pS, the estimated maximum flux of Ca2+ in a Ca2+ spot (0.4 x 10-17 to 4.7 x 10-17 mol x s(-1)) was comparable to currents of one or a few MS channels. On real-time three-dimensional confocal imaging analysis, which permitted simultaneous imaging of basal and apical planes of cells at 37.6 ms intervals, Ca2+ spots on the apical plane were more clearly visualized than those on the basal plane. From these results, we propose that the Ca2+ spot is an elementary Ca2+-influx event through MS channels directly coupled with the first step in mechanoreception In addition, our results strongly suggest that LPA functions as an endogenous factor affecting mechanotransduction systems.
在机械应力作用下,利用实时共聚焦显微镜在生物活性溶血磷脂酸(LPA)存在的情况下,清晰地观察到牛晶状体上皮细胞内几个区域的细胞内Ca2 +浓度([Ca2 +] i)局部升高。我们将这种现象称为“Ca2 +斑点”。Ca2 +斑点始于半径约为1.5μm的圆形区域。这些Ca2 +斑点同心扩散,导致[Ca2 +] i平均整体升高。局部升高通常以逐步方式或在同一区域重复出现。Ca2 +斑点的时空特性与ATP(一种Ca2 +动员激动剂)诱导的Ca2 +波完全不同。通过降低细胞外Ca2 +浓度或通过机械敏感(MS)通道抑制剂Gd3 +的存在可抑制Ca2 +斑点,但内质网Ca2 +泵抑制剂毒胡萝卜素则不能抑制,这表明Ca2 +斑点源于通过Gd3 +敏感的MS通道的Ca2 +内流。假设在晶状体上皮细胞中,MS通道的开放概率为0.4,膜电位为56 mV,通道电导为50 pS,则Ca2 +斑点中Ca2 +的估计最大通量(0.4×10-17至4.7×10-17 mol·s(-1))与一个或几个MS通道的电流相当。在实时三维共聚焦成像分析中,该分析允许以37.6 ms的间隔同时对细胞的基底和顶面进行成像,顶面上的Ca2 +斑点比底面上的更清晰可见。根据这些结果,我们提出Ca2 +斑点是通过与机械感受第一步直接耦合的MS通道的基本Ca2 +内流事件。此外,我们的结果强烈表明LPA作为影响机械转导系统的内源性因子发挥作用。