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首页> 外文期刊>The Journal of Physiology >Sources of protons and a role for bicarbonate in inhibitory feedback from horizontal cells to cones in Ambystoma tigrinum retina
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Sources of protons and a role for bicarbonate in inhibitory feedback from horizontal cells to cones in Ambystoma tigrinum retina

机译:质子的来源和碳酸氢盐在视网膜小白鼠视网膜水平细胞向视锥细胞的抑制性反馈中的作用

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摘要

Lateral-inhibitory feedback from horizontal cells (HCs) to photoreceptors involves changes in synaptic cleft pH accompanying light-evoked changes in HC membrane potential. We analysed HC to cone feedback by studying surround-evoked light responses of cones and by obtaining paired whole cell recordings from cones and HCs in salamander retina. We tested three potential sources for synaptic cleft protons: (1) generation by extracellular carbonic anhydrase (CA), (2) release from acidic synaptic vesicles and (3) Na+/H+ exchangers (NHEs). Neither antagonizing extracellular CA nor blocking loading of protons into synaptic vesicles eliminated feedback. However, feedback was eliminated when extracellular Na+ was replaced with choline and significantly reduced by an NHE inhibitor, cariporide. Depriving NHEs of intracellular protons by buffering HC cytosol with a pH 9.2 pipette solution eliminated feedback, whereas alkalinizing the cone cytosol did not, suggesting that HCs are a major source for protons in feedback. We also examined mechanisms for changing synaptic cleft pH in response to changes in HC membrane potential. Increasing the trans-membrane proton gradient by lowering the extracellular pH from 7.8 to 7.4 to 7.1 strengthened feedback. While maintaining constant extracellular pH with 1 mM HEPES, removal of bicarbonate abolished feedback. Elevating intracellular bicarbonate levels within HCs prevented this loss of feedback. A bicarbonate transport inhibitor, 4,4'-diisothiocyano-2,2'-stilbenedisulfonic acid (DIDS), also blocked feedback. Together, these results suggest that NHEs are the primary source of extracellular protons in HC feedback but that changes in cleft pH accompanying changes in HC membrane voltage also require bicarbonate flux across the HC membrane.
机译:从水平细胞(HCs)到光感受器的侧向抑制性反馈涉及伴随着HC膜电位的光诱发变化的突触裂pH的变化。我们通过研究视锥细胞的周围环境诱发的光反应,以及从sal和视网膜中的视锥细胞和HCs中获得成对的全细胞记录,来分析HC对视锥细胞的反馈。我们测试了突触裂质子的三种潜在来源:(1)通过细胞外碳酸酐酶(CA)产生,(2)从酸性突触小泡释放和(3)Na + / H +交换子(NHE)。既不拮抗细胞外CA,也不阻止质子装载到突触小泡中,不能消除反馈。但是,当细胞外的Na +被胆碱替代并被NHE抑制剂cariporide显着降低时,反馈被消除了。通过用pH 9.2移液器缓冲HC胞质溶液来剥夺NHEs的细胞内质子,可以消除反馈,而碱化视锥细胞质则不能,这表明HCs是质子反馈的主要来源。我们还研究了响应于HC膜电位变化而改变突触间隙pH的机制。通过将细胞外pH从7.8降低到7.4到7.1,来增加跨膜质子梯度,从而增强了反馈。用1 mM HEPES维持恒定的细胞外pH值时,去除碳酸氢盐消除了反馈。 HC内细胞内碳酸氢盐水平的升高阻止了这种反馈的损失。碳酸氢盐转运抑制剂4,4'-diisothiocyano-2,2'-stilbenedisulfonic acid(DIDS)也阻止了反馈。总之,这些结果表明,NHE是HC反馈中胞外质子的主要来源,但伴随HC膜电压变化的裂缝pH的变化也需要碳酸氢盐通量穿过HC膜。

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