Department of Biology, Lake Forest College, 555 N. Sheridan Road, Lake Forest, IL 60045, USA.
J Membr Biol. 2011 Mar;240(1):1-12. doi: 10.1007/s00232-010-9336-4. Epub 2010 Dec 10.
The American alligator can hibernate during winter, which may lead to osmotic imbalance because of reduced kidney function and lack of food consumption during this period. Accordingly, we hypothesized that their red blood cells would have a well-developed regulatory volume decrease (RVD) to cope with the homeostatic challenges associated with torpor. Osmotic fragility was determined optically, mean cell volume was measured by electronic sizing, and changes in intracellular Ca²+ concentration were visualized using fluorescence microscopy and fluo-4-AM. Osmotic fragility increased and the ability to regulate volume was inhibited when extracellular Na+ was replaced with K+, or when cells were exposed to the K+ channel inhibitor quinine, indicating a requirement of K+ efflux for RVD. Addition of the ionophore gramicidin to the extracellular medium decreased osmotic fragility and also potentiated volume recovery, even in the presence of quinine. In addition, hypotonic shock (0.5 x Ringer) caused an increase in cytosolic Ca²+, which resulted from Ca²+ influx because it was not observed when extracellular Ca²+ was chelated with EGTA (ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraacetic acid). Furthermore, cells loaded with BAPTA-AM (1,2-bis(2-aminophenoxymethyl)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl) ester) or exposed to a low Ca²+-EGTA hypotonic Ringer had a greater osmotic fragility and also failed to recover from cell swelling, indicating that extracellular Ca²+ was needed for RVD. Gramicidin reversed the inhibitory effect of low extracellular Ca²+. Finally, and surprisingly, the Ca²+ ionophore A23187 increased osmotic fragility and inhibited volume recovery. Taken together, our results show that cell swelling activated a K+ permeable pathway via a Ca²+-dependent mechanism, and this process mediated K+ loss during RVD.
美洲鳄在冬季可以冬眠,由于在此期间肾功能下降和食物摄入减少,可能会导致渗透失衡。因此,我们假设它们的红细胞会有一个发达的调节体积减少(RVD)来应对与蛰伏相关的体内平衡挑战。渗透压脆性通过光学方法确定,平均细胞体积通过电子测量,细胞内 Ca²+浓度的变化通过荧光显微镜和 fluo-4-AM 可视化。当细胞外液中的 Na+被 K+取代,或当细胞暴露于 K+通道抑制剂奎宁时,渗透压脆性增加,体积调节能力受到抑制,表明 RVD 需要 K+外流。将离子载体短杆菌肽添加到细胞外介质中会降低渗透压脆性,并增强体积恢复,即使在存在奎宁的情况下也是如此。此外,低渗冲击(0.5 x Ringer)会导致细胞溶质 Ca²+增加,这是由于 Ca²+内流引起的,因为当细胞外液中的 Ca²+与 EGTA(乙二醇双(2-氨基乙氧基)乙醚-N,N,N',N'-四乙酸)螯合时,不会观察到这种情况。此外,用 BAPTA-AM(1,2-双(2-氨基苯氧基甲基)乙烷-N,N,N',N'-四乙酸四(乙酰氧甲基)酯)加载的细胞或暴露于低 Ca²+-EGTA 低渗 Ringer 中,渗透压脆性更大,并且不能从细胞肿胀中恢复,这表明 RVD 需要细胞外液 Ca²+。短杆菌肽逆转了低细胞外液 Ca²+的抑制作用。最后,令人惊讶的是,Ca²+载体 A23187 增加了渗透压脆性并抑制了体积恢复。总之,我们的结果表明,细胞肿胀通过 Ca²+依赖性机制激活了一种 K+渗透性途径,并且该过程在 RVD 期间介导了 K+的损失。