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培养的人上皮细胞中的容积调节性氯离子通道电流

Volume-regulatory Cl- channel currents in cultured human epithelial cells.

作者信息

Kubo M, Okada Y

机构信息

Department of Physiology, Kyoto University Faculty of Medicine, Japan.

出版信息

J Physiol. 1992 Oct;456:351-71. doi: 10.1113/jphysiol.1992.sp019340.

Abstract
  1. During osmotic swelling, cultured human small intestinal epithelial cells (Intestine 407) exhibited activation of large Cl- currents under the patch-clamp whole-cell configuration. The volume-sensitive Cl- conductance was independent of intracellular Ca2+ and cyclic AMP. 2. The anion permeability sequence of the current was SCN- > I- > Br- > Cl- > F- > gluconate-, corresponding to Eisenman's sequence I. 3. Cl- currents were instantaneously activated by command pulses in a range of -120 to +45 mV. At potentials more positive than +50 mV the current showed a time-dependent inactivation. This inactivation was accelerated by increased depolarization. The instantaneous current-voltage relationship rectified in the outward direction. 4. A stilbene-derivative Cl- channel blocker, 4-acetamido-4'-isothiocyanostilbene (SITS), inhibited the Cl- current at micromolar concentrations. SITS facilitated inactivation at positive potentials. Outward currents were more prominently suppressed by SITS than inward currents. The concentrations required for 50% inhibition (IC50) of outward and inward currents were 1.5 and 6 microM, respectively. The outward and inward currents were equally inhibited by a carboxylate analogue Cl- channel blocker, 5-nitro-2-(3-phenylpropylamino)-benzoate (NPPB) or diphenylamine-2-carboxylate (DPC) at higher doses (IC50 = 25 for NPPB or 350 microM for DPC). Inactivation kinetics at large depolarizations was not affected by NPPB or DPC. 5. The Cl- current was blocked by an unsaturated fatty acid, arachidonic acid (IC50 = 8 microM). Arachidonic acid was still effective in the presence of inhibitors of lipoxygenase (nordihydroguaiaretic acid, 10 microM), cyclo-oxygenase (indomethacin, 10 microM) and protein kinase C (polymyxin B, 30 microM). The Cl- current was also sensitive to another cis unsaturated fatty acid, oleic acid, which is not a substrate for oxygenases. A trans isomer of oleate, elaidic acid, and a saturated fatty acid, palmitic acid, were ineffective. 6. Single Intestine 407 cells exposed to a hypotonic solution showed a regulatory volume decrease after initial osmotic swelling. The volume regulation was abolished by SITS, NPPB, arachidonate and oleate, but not by elaidate and palmitate. 7. It is concluded that outwardly rectifying Cl- channels, which are sensitive to arachidonic acid, are activated upon osmotic swelling and involved in the subsequent cell volume regulation.
摘要
  1. 在渗透性肿胀过程中,培养的人小肠上皮细胞(Intestine 407)在膜片钳全细胞模式下表现出大的氯离子电流激活。容积敏感性氯离子电导与细胞内钙离子和环磷酸腺苷无关。2. 该电流的阴离子通透性顺序为硫氰酸根>碘离子>溴离子>氯离子>氟离子>葡萄糖酸盐,与艾森曼序列I相对应。3. 在-120至+45 mV范围内的指令脉冲可瞬间激活氯离子电流。在电位高于+50 mV时,电流呈现时间依赖性失活。这种失活因去极化增强而加速。瞬时电流-电压关系在向外方向呈整流性。4. 一种芪衍生物氯离子通道阻滞剂4-乙酰氨基-4'-异硫氰酸芪(SITS)在微摩尔浓度下可抑制氯离子电流。SITS促进正电位下的失活。向外电流比向内电流更显著地被SITS抑制。向外和向内电流50%抑制所需浓度(IC50)分别为1.5和6 microM。较高剂量时,羧酸盐类似物氯离子通道阻滞剂5-硝基-2-(3-苯丙基氨基)-苯甲酸盐(NPPB)或二苯胺-2-羧酸盐(DPC)对向外和向内电流的抑制作用相同(NPPB的IC50 = 25 microM,DPC的IC5 = 350 microM)。大去极化时的失活动力学不受NPPB或DPC影响。5. 氯离子电流被不饱和脂肪酸花生四烯酸(IC50 = 8 microM)阻断。在脂氧合酶抑制剂(去甲二氢愈创木酸,10 microM)、环氧化酶抑制剂(吲哚美辛,10 microM)和蛋白激酶C抑制剂(多粘菌素B,30 microM)存在的情况下,花生四烯酸仍然有效。氯离子电流对另一种顺式不饱和脂肪酸油酸也敏感,油酸不是氧化酶的底物。油酸的反式异构体反油酸和饱和脂肪酸棕榈酸无效。6. 暴露于低渗溶液的单个Intestine 407细胞在初始渗透性肿胀后显示出调节性容积减小。SITS、NPPB、花生四烯酸盐和油酸盐可消除容积调节,但反油酸盐和棕榈酸盐则不能。7. 得出结论,对花生四烯酸敏感的向外整流氯离子通道在渗透性肿胀时被激活,并参与随后的细胞容积调节。

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