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首页> 外文期刊>Glia >The Speed of Swelling Kinetics Modulates Cell Volume Regulation and Calcium Signaling in Astrocytes: A Different Point of View on the Role of Aquaporins
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The Speed of Swelling Kinetics Modulates Cell Volume Regulation and Calcium Signaling in Astrocytes: A Different Point of View on the Role of Aquaporins

机译:膨胀动力学的速度调节星形胶质细胞的细胞体积调节和钙信号传导:关于水通道蛋白的作用的不同观点

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摘要

Regulatory volume decrease (RVD) is a process by which cells restore their original volume in response to swelling. In this study, we have focused on the role played by two different Aquaporins (AQPs), Aquaporin-4 (AQP4), and Aquaporin-1 (AQP1), in triggering RVD and in mediating calcium signaling in astrocytes under hypotonic stimulus. Using biophysical techniques to measure water flux through the plasma membrane of wild-type (WT) and AQP4 knockout (KO) astrocytes and of an astrocyte cell line (DI TNC1) transfected with AQP4 or AQP1, we here show that AQP-mediated fast swelling kinetics play a key role in triggering and accelerating RVD. Using calcium imaging, we show that AQP-mediated fast swelling kinetics also significantly increases the amplitude of calcium transients inhibited by Gadolinium and Ruthenium Red, two inhibitors of the transient receptor potential vanilloid 4 (TRPV4) channels, and prevented by removing extracellular calcium. Finally, inhibition of TRPV4 or removal of extracellular calcium does not affect RVD. All together our study provides evidence that (1) AQP influenced swelling kinetics is the main trigger for RVD and in mediating calcium signaling after hypotonic stimulus together with TRPV4, and (2) calcium influx from the extracellular space and/or TRPV4 are not essential for RVD to occur in astrocytes. Main Points: (1) The speed of swelling kinetics is the main trigger for Regulatory Volume Decrease (RVD) and for calcium response in astrocytes; (2) Calcium influx from the extracellular space and TRPV4 are not essential for RVD.
机译:调节体积减少(RVD)是细胞响应肿胀而恢复其原始体积的过程。在这项研究中,我们集中于两种不同的水通道蛋白(AQPs),水通道蛋白4(AQP4)和水通道蛋白1(AQP1)在低渗刺激下触发RVD和介导星形胶质细胞钙信号中的作用。使用生物物理技术测量通过野生型(WT)和AQP4敲除(KO)星形胶质细胞以及转染了AQP4或AQP1的星形胶质细胞系(DI TNC1)质膜的水通量,我们在这里显示了AQP介导的快速肿胀动力学在触发和加速RVD中起关键作用。使用钙成像,我们显示AQP介导的快速溶胀动力学也显着增加了by和钌红(瞬时受体电位香草酸4(TRPV4)通道的两种抑制剂)抑制的钙瞬变幅度,并通过去除细胞外钙阻止了钙瞬变的幅度。最后,抑制TRPV4或去除细胞外钙不会影响RVD。总之,我们的研究提供了证据:(1)AQP影响的溶胀动力学是RVD的主要触发因素,并且是在与TRPV4一起引起低渗刺激后介导钙信号传导的因素;(2)来自细胞外空间和/或TRPV4的钙流入对于RVD发生在星形胶质细胞中。要点:(1)膨胀动力学的速度是星形胶质细胞调节体积减少(RVD)和钙反应的主要诱因; (2)来自细胞外空间的钙流入和TRPV4对于RVD并非必需。

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