Trautmann A, Marty A
Proc Natl Acad Sci U S A. 1984 Jan;81(2):611-5. doi: 10.1073/pnas.81.2.611.
Electrical properties of the membranes of lacrimal gland cells were investigated using patch-clamp techniques [Hamill, O.P., Marty A., Neher, E., Sakmann, B. & Sigworth, F.J. (1981) Pflügers Arch. 391, 85-100]. The membranes were found to contain a specific kind of voltage- and Ca2+ -activated K+ channel ("BK channels"). These channels account for the strong rectification of the cell current-voltage curve as obtained in tight-seal whole-cell recordings. Application of low concentrations of carbamoylcholine (CbmCho, 0.5 microM) activated the BK channels. No effect was obtained in the presence of atropine (2 microM) or when dialyzing the cell with a strong CaEGTA buffer. The latter result, together with other findings, suggests that CbmCho exerts its action on BK channels by increasing the intracellular Ca2+ concentration. This Ca2+ concentration increase presumably occurred via liberation from a cytoplasmic Ca2+ store, because the response remained unaffected in the absence of extracellular Ca2+. At higher CbmCho concentration (2 microM), an inward current was observed, which was assumed to result from activation of another type of Ca2+ -regulated channel.
利用膜片钳技术[哈米尔,O.P.,马蒂,A.,内尔,E.,萨克曼,B.和西格沃思,F.J.(1981年)《普弗吕格尔斯·阿赫》391,85 - 100]研究了泪腺细胞膜的电特性。发现这些膜含有一种特定类型的电压和Ca2 +激活的钾通道(“BK通道”)。这些通道解释了在紧密封全细胞记录中获得的细胞电流 - 电压曲线的强整流现象。应用低浓度的氨甲酰胆碱(CbmCho,0.5微摩尔)可激活BK通道。在存在阿托品(2微摩尔)时或用强CaEGTA缓冲液透析细胞时没有效果。后一结果与其他发现一起表明,CbmCho通过增加细胞内Ca2 +浓度对BK通道发挥作用。这种Ca2 +浓度的增加可能是通过从细胞质Ca2 +储存库释放而发生的,因为在没有细胞外Ca2 +的情况下反应仍然不受影响。在较高的CbmCho浓度(2微摩尔)下,观察到内向电流,这被认为是由另一种类型的Ca2 +调节通道的激活引起的。