Jia Yousheng, Jeng Jade-Ming, Sensi Stefano L, Weiss John H
Department of Neurology, University of California at Irvine, CA 92697-4292, USA.
J Physiol. 2002 Aug 15;543(Pt 1):35-48. doi: 10.1113/jphysiol.2002.020172.
Permeation of the endogenous cation Zn2+ through calcium-permeable AMPA/kainate receptor-gated (Ca-A/K) channels might subserve pathological and/or physiological signalling roles. Voltage-clamp recording was used to directly assess Zn2+ flux through these channels on cultured murine hippocampal neurones. Ca-A/K channels were present in large numbers only on a minority of neurones (Ca-A/K+ neurones), many of which were GABAergic. The presence of these channels was assessed in whole-cell or outside-out patch recording as the degree of inward rectification of kainate-activated currents, quantified via a rectification index (RI = G+40/G-60), which ranged from <0.4 (strongly inwardly rectifying) to >2 (outwardly rectifying). The specificity of a low RI as an indication of robust Ca-A/K channel expression was verified by two other techniques, kainate-stimulated cobalt-uptake labelling, and fluorescence imaging of kainate-induced increases in intracellular Ca2+. In addition, the degree of inward rectification of kainate-activated currents correlated strongly with the positive shift of the reversal potential (V(rev)) upon switching to a sodium-free, 10 mM Ca2+ buffer. With Zn2+ (3 mM) as the only permeant extracellular cation, kainate-induced inward currents were only observed in neurones that had previously been identified as Ca-A/K+. A comparison between the V(rev) observed with 3 mM Zn2+ and that observed with Ca2+ as the permeant cation revealed a P(Ca)/P(Zn) of approximately 1.8. Inward currents recorded in 3 mM Ca2+ were unaffected by the addition of 0.3 mM Zn2+, while microfluorimetrically detected increases in the intracellular concentration of Zn2+ in Ca-A/K+ neurones upon kainate exposure in the presence of 0.3 mM Zn2+ were only mildly attenuated by the addition of 1.8 mM Ca2+. These results provide direct evidence that Zn2+ can carry currents through Ca-A/K channels, and that there is little interference between Ca2+ and Zn2+ in permeating these channels.
内源性阳离子Zn2+通过钙通透性AMPA/海人酸受体门控(Ca-A/K)通道的渗透可能具有病理和/或生理信号传导作用。采用电压钳记录法直接评估培养的小鼠海马神经元中Zn2+通过这些通道的通量。Ca-A/K通道仅大量存在于少数神经元(Ca-A/K+神经元)上,其中许多是γ-氨基丁酸能神经元。在全细胞或外向膜片钳记录中,通过整流指数(RI = G+40/G-60)量化海人酸激活电流的内向整流程度来评估这些通道的存在,该指数范围从<0.4(强内向整流)到>2(外向整流)。通过另外两种技术,即海人酸刺激的钴摄取标记和海人酸诱导的细胞内Ca2+增加的荧光成像,验证了低RI作为强大的Ca-A/K通道表达指标的特异性。此外,海人酸激活电流的内向整流程度与切换到无钠的10 mM Ca2+缓冲液时反转电位(V(rev))的正向偏移密切相关