Department of Biology, Indiana Wesleyan University, 4201 South Washington Street, Marion, IN 46953, USA.
Eur J Neurosci. 2012 Oct;36(8):3040-50. doi: 10.1111/j.1460-9568.2012.08226.x. Epub 2012 Jul 19.
The H(+) hypothesis of lateral feedback inhibition in the outer retina predicts that depolarizing agents should increase H(+) release from horizontal cells. To test this hypothesis, self-referencing H(+) -selective microelectrodes were used to measure extracellular H(+) fluxes from isolated goldfish horizontal cells. We found a more complex pattern of cellular responses than previously observed from horizontal cells of other species examined using this technique. One class of cells had an initial standing signal indicative of high extracellular H(+) adjacent to the cell membrane; challenge with glutamate, kainate or high extracellular potassium induced an extracellular alkalinization. This alkalinization was reduced by the calcium channel blockers nifedipine and cobalt. A second class of cells displayed spontaneous oscillations in extracellular H(+) that were abolished by cobalt, nifedipine and low extracellular calcium. A strong correlation between changes in intracellular calcium and extracellular proton flux was detected in experiments simultaneously monitoring intracellular calcium and extracellular H(+) . A third set of cells was characterized by a standing extracellular alkalinization which was turned into an acidic signal by cobalt. In this last set of cells, addition of glutamate or high extracellular potassium did not significantly alter the proton signal. Taken together, the response characteristics of all three sets of neurons are most parsimoniously explained by activation of a plasma membrane Ca(2+) ATPase pump, with an extracellular alkalinization resulting from exchange of intracellular calcium for extracellular H(+) . These findings argue strongly against the hypothesis that H(+) release from horizontal cells mediates lateral inhibition in the outer retina.
外网状层横向反馈抑制的 H(+)假说预测,去极化剂应该增加水平细胞的 H(+)释放。为了检验这一假说,我们使用自我参照 H(+)选择性微电极测量了来自分离的金鱼水平细胞的细胞外 H(+)通量。我们发现了一种比以前用这种技术观察到的其他物种的水平细胞更复杂的细胞反应模式。一类细胞具有细胞膜附近高细胞外 H(+)的初始静止信号;用谷氨酸、海人酸或高细胞外钾刺激会引起细胞外碱化。这种碱化被钙通道阻滞剂硝苯地平和钴减少。第二类细胞显示出细胞外 H(+)的自发振荡,这种振荡被钴、硝苯地平和低细胞外钙消除。在同时监测细胞内钙和细胞外 H(+)的实验中检测到细胞内钙变化与细胞外质子通量之间的强相关性。第三组细胞的特征是细胞外静止性碱化,这种碱化被钴转化为酸性信号。在最后一组细胞中,添加谷氨酸或高细胞外钾并没有显著改变质子信号。总的来说,所有三组神经元的反应特征都可以通过激活质膜 Ca(2+)ATP 酶泵来最好地解释,其结果是通过细胞内钙与细胞外 H(+)的交换导致细胞外碱化。这些发现强烈反对水平细胞 H(+)释放介导外网状层横向抑制的假说。