Mola Maria Grazia, Sparaneo Angelo, Gargano Concetta Domenica, Spray David C, Svelto Maria, Frigeri Antonio, Scemes Eliana, Nicchia Grazia Paola
Department of Bioscience, Biotechnology, and Biopharmaceutics, University of Bari "Aldo Moro,", Bari, Italy.
Laboratory of Oncology, IRCCS Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Italy.
Glia. 2016 Jan;64(1):139-54. doi: 10.1002/glia.22921. Epub 2015 Sep 28.
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.
调节性容积减小(RVD)是细胞在肿胀时恢复其原始容积的过程。在本研究中,我们聚焦于两种不同的水通道蛋白(AQP),即水通道蛋白4(AQP4)和水通道蛋白1(AQP1),在低渗刺激下触发星形胶质细胞的RVD以及介导钙信号传导中所起的作用。我们使用生物物理技术测量野生型(WT)和AQP4基因敲除(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,在此表明AQP介导的快速肿胀动力学在触发和加速RVD中起关键作用。通过钙成像,我们表明AQP介导的快速肿胀动力学还显著增加了被钆和钌红抑制的钙瞬变幅度,钆和钌红是瞬时受体电位香草酸受体4(TRPV4)通道的两种抑制剂,并且通过去除细胞外钙可防止这种情况。最后,抑制TRPV4或去除细胞外钙并不影响RVD。我们的研究总体上提供了证据,即(1)AQP影响的肿胀动力学是RVD的主要触发因素,并且在低渗刺激后与TRPV4一起介导钙信号传导,以及(2)细胞外空间的钙内流和/或TRPV4对于星形胶质细胞中RVD的发生并非必不可少。