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Synergetic activation of outwardly rectifying Cl− currents by hypotonic stress and external Ca2+ in murine osteoclasts

机译:低渗应激和小鼠破骨细胞中外部Ca2 +协同向外激活Cl-电流的激活

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摘要

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).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.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.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.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).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:低渗刺激激活了鼠破骨细胞的向外整流的Cl-(ORC1)电流。低电流激活的ORCl电流通过无ATP移液器的细胞内透析抑制而被低渗激活的ORCl电流抑制,该电流具有快速活化,极小的失活,强烈的向外整流,被DIDS阻滞和对有机酸(丙酮酸和谷氨酸)的渗透性的特征。用难水解的ATP类似物腺苷5'-O-(3-硫代三磷酸)替代ATP。当pH在6.6-8.0范围内时,细胞内碱度增加时,电流幅度减小。细胞内松弛素D的细胞内应用偶尔会激活ORCl电流,而不会出现低渗应激,但会通过低渗刺激抑制ORCl电流的激活。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。细胞外Ca2 +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。通过20 mm EGTA进行细胞内透析,低渗激活的ORCl电流部分降低。在细胞外培养基中存在10 mm Ca2 +时,ORCl电流被激活,这是因为渗透压降低的幅度比1 mm Ca2 +小得多。对低渗敏感性的增加可以通过增加细胞内Ca2 +水平(pCa 6.5)来模拟。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ORCl通道,并且激活过程被多种因素修饰。细胞内因子(pH,ATP和肌动蛋白细胞骨架组织)。

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