Maximov A V, Vedernikova E A, Hinssen H, Khaitlina S Y, Negulyaev Y A
Institute of Cytology, Russian Academy of Sciences, St.-Petersburg, Russian Federation.
FEBS Lett. 1997 Jul 21;412(1):94-6. doi: 10.1016/s0014-5793(97)00754-0.
With the use of the patch-clamp technique, physiological mechanisms of Na+ channel regulation involving submembranous actin rearrangements were examined in human myeloid leukemia K562 cells. We found that the actin-severing protein gelsolin applied to cytoplasmic surface of membrane fragments at a high level of [Ca2+]i (1 microM) increased drastically the activity of Na-selective channels of 12 pS unitary conductance. In the experiments on intact cells, the elevation of [Ca2+]i using the ionophore 4Br-A23187 also resulted in Na+ channel activation. Addition of actin to the cytoplasmic surface of membrane patches reduced this activity to background level, likely due to actin polymerization. Our data imply that Ca-dependent modulations of the actin cytoskeleton may represent one of the general mechanisms of channel regulation and cell signalling.
利用膜片钳技术,在人髓系白血病K562细胞中研究了涉及膜下肌动蛋白重排的Na⁺通道调节的生理机制。我们发现,在高浓度[Ca²⁺]i(1微摩尔)下,将肌动蛋白切割蛋白凝溶胶蛋白应用于膜片段的细胞质表面,可显著增加12 pS单位电导的Na⁺选择性通道的活性。在完整细胞实验中,使用离子载体4Br-A23187升高[Ca²⁺]i也会导致Na⁺通道激活。向膜片的细胞质表面添加肌动蛋白可将这种活性降低至背景水平,这可能是由于肌动蛋白聚合所致。我们的数据表明,肌动蛋白细胞骨架的钙依赖性调节可能是通道调节和细胞信号传导的一般机制之一。