Cecilie Bugge Bakketun, Lena Catherine Roth, Daniel Marelius Bjørnstad, Ole Petter Ottersen, Vidar Jensen, Rune Enger
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引用次数: 0
摘要
星形胶质细胞随着细胞外K+浓度的升高而膨胀。这种K+诱导的肿胀被广泛认为是由于星形细胞摄取K+,即使其潜在的机制尚未完全了解。关于脑水通道AQP4在K+诱导的肿胀中的作用,已经提出了相互矛盾的结果。这需要重新审视AQP4在K+诱导的星形细胞肿胀动力学中的作用。在这项研究中,我们对野生型(WT)和Aqp4-/-小鼠的急性海马切片进行了双光子显微镜观察,以评估中高10 mM和病理高50 mM [K+]溶液对星形胶质细胞肿胀的反应。我们证明,与WT相比,暴露于10 mM [K+]o的Aqp4-/-星形胶质细胞中K+诱导的肿胀减弱。在暴露于50 mM [K+]o的切片中,两种基因型之间的峰值肿胀相似,而Aqp4-/-星形胶质细胞的细胞体积恢复更完全。我们证明了两种[K+]浓度引起的星形细胞Ca2+信号反应根本不同,并且在10 mM [K+]o的情况下,Ca2+信号反应在基因型之间是不同的。我们的研究结果表明,K+诱导的星形胶质细胞肿胀具有不同的机制基础,这取决于星形胶质细胞所暴露的K+浓度,而改变的星形胶质细胞Ca2+信号是一种可能的机制。
The Impact of Aquaporin-4 Deletion on K+-Induced Astrocytic Swelling Depends on K+ Concentration.
Astrocytes swell in response to elevations in extracellular K+ concentration. This K+-induced swelling is widely believed to be due to astrocytic K+ uptake, even if the underlying mechanisms are not fully understood. Conflicting results pertaining to the role of the brain water channel AQP4 in K+-induced swelling have been presented. This calls for revisiting the effect of AQP4 on K+-induced astrocytic swelling dynamics. In this study, we performed two-photon microscopy of acute hippocampal slices from wildtype (WT) and Aqp4-/- mice to assess astrocytic swelling in response to medium high 10 mM and pathologically high 50 mM [K+] solutions. We demonstrate that K+-induced swelling is attenuated in Aqp4-/- astrocytes exposed to 10 mM [K+]o compared to WT. In slices exposed to 50 mM [K+]o, peak swelling was similar between the two genotypes, whereas the cell volume recovery was more complete in Aqp4-/- astrocytes. We demonstrate that the two [K+] concentrations elicit fundamentally different astrocytic Ca2+ signaling responses, and that the Ca2+ signaling response differs between the genotypes in the 10 mM [K+]o scenario. Our findings suggest that K+-induced astrocytic swelling has different mechanistic underpinnings, depending on the K+ concentration to which the astrocytes are exposed, and that altered astrocytic Ca2+ signaling is a putative mechanism involved.
期刊介绍:
GLIA is a peer-reviewed journal, which publishes articles dealing with all aspects of glial structure and function. This includes all aspects of glial cell biology in health and disease.