首页> 外文期刊>The Journal of Physiology >Synergetic activation of outwardly rectifying Cl- currents by hypotonic stress and external Ca2+ in murine osteoclasts.
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Synergetic activation of outwardly rectifying Cl- currents by hypotonic stress and external Ca2+ in murine osteoclasts.

机译:低渗应激和鼠破骨细胞中外部Ca2 +协同激活向外整流的Cl-电流。

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1. An outwardly rectifying Cl- (ORCl) current of murine osteoclasts was activated by hypotonic stimulation. The current was characterized by rapid activation, little inactivation, strong outward rectification, blockage by DIDS and permeability to organic acids (pyruvate and glutamate). 2. The hypotonically activated ORCl current was inhibited by intracellular dialysis with an ATP-free pipette solution, but not by replacement of ATP with a poorly hydrolysable ATP analogue adenosine 5'-O-(3-thiotriphosphate). The current amplitude was reduced when intracellular alkalinity increased over the pH range 6.6-8.0. 3. Intracellular application of cytochalasin D occasionally activated the ORCl current without hypotonic stress, but inhibited activation of the ORCl current by hypotonic stimulation. The hypotonically activated ORCl current was unaffected by a non-actin-depolymerizing cytochalasin, chaetoglobosin C, but partially inhibited by deoxyribonuclease I. 4. Removal of extracellular Ca2+ inhibited activation of the ORCl current by hypotonic shock, but did not reduce the current once activated. The hypotonically activated ORCl current was partially decreased by intracellular dialysis with 20 mM EGTA. 5. With 10 mM Ca2+ in the extracellular medium, the ORCl current was activated in response to more minor decreases in osmolarity than with 1 mM Ca2+. The increased sensitivity to hypotonicity was mimicked by increasing the intracellular Ca2+ level (pCa 6.5). 6. These results suggest that hypotonic stimulation and a rise in the extracellular Ca2+ level synergistically activate the ORCl channel of murine osteoclasts, and that the activating process is modified by multiple intracellular factors (pH, ATP and actin cytoskeletal organization).
机译:1.低渗刺激激活了鼠破骨细胞的向外整流的Cl-(ORC1)电流。该电流的特征在于快速活化,几乎没有失活,强烈的向外整流,被DIDS阻挡以及对有机酸(丙酮酸和谷氨酸)的渗透性。 2.通过无ATP移液器的细胞内透析抑制低渗活化的ORCl电流,但不通过用难水解的ATP类似物腺苷5'-O-(3-硫代三磷酸)替代ATP来抑制。当细胞内碱度在6.6-8.0的pH范围内增加时,电流幅度减小。 3.胞内松弛素D的细胞内施用偶尔激活了ORCl电流而没有低渗应激,但是通过低渗刺激抑制了ORCl电流的活化。低渗激活的ORCl电流不受非肌动蛋白解聚的细胞松弛素chaetoglobosin C的影响,但被脱氧核糖核酸酶I部分抑制。4.细胞外Ca 2+的去除抑制了低渗性休克对ORCl电流的激活,但一旦激活则不会降低电流。低渗活化的ORCl电流通过用20mM EGTA进行细胞内透析而部分降低。 5.在细胞外培养基中具有10mM Ca 2+时,响应于与1mM Ca 2+相比较小的渗透压降低,激活了ORCl电流。通过降低细胞内Ca2 +水平(pCa 6.5)可以模仿对低渗症的敏感性增加。 6.这些结果表明,低渗刺激和细胞外Ca2 +水平的升高可以协同激活鼠破骨细胞的ORC1通道,并且激活过程受到多种细胞内因子(pH,ATP和肌动蛋白细胞骨架组织)的影响。

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