Nakanishi S, Fujii A, Kimura T, Sakakibara S, Mikoshiba K
Pharmaceutical Basic Research Laboratories, JT, Inc., Kanagawa, Japan.
J Neurosci Res. 1995 Jul 1;41(4):532-9. doi: 10.1002/jnr.490410413.
A peptide toxin derived from funnel-web spider venom, omega-agatoxin IVA, blocks voltage-sensitive calcium channels. Many pharmacological and electrophysiological studies have shown that these channels are widely distributed in both the central nervous system (CNS) and neuromuscular junctions. However, a direct morphological demonstration of the binding sites of this toxin is still lacking. To identify which cells have the binding sites, a biologically active, biotin-conjugated omega-agatoxin IVA was applied to mouse cerebellar and hippocampal slices. Confocal microscopy revealed that omega-agatoxin IVA binding sites were distributed on the somata of Purkinje cells, cerebellar granule cells and interneurons, as well as on the dendrites of Purkinje cells. In the hippocampus, the binding sites were localized on the somata of pyramidal cells of the CA1-CA4 region and on the somata of granule cells in the dentate gyrus. A sequential competitive reaction confirmed the specificity of the binding in the cerebellum and CA1 pyramidal cells, and also suggested a difference in the binding affinity between CA1 and CA3 pyramidal cells. Since a high concentration of omega-agatoxin IVA (2 microM) was needed for the present study, the omega-agatoxin IVA binding sites presented in this study may represent "P-type" and "Q-type" calcium channels.
一种源自漏斗网蜘蛛毒液的肽毒素——ω-阿加毒素IVA,可阻断电压敏感性钙通道。许多药理学和电生理学研究表明,这些通道广泛分布于中枢神经系统(CNS)和神经肌肉接头处。然而,该毒素结合位点的直接形态学证据仍然缺乏。为了确定哪些细胞具有结合位点,将具有生物活性的、生物素偶联的ω-阿加毒素IVA应用于小鼠小脑和海马切片。共聚焦显微镜显示,ω-阿加毒素IVA结合位点分布在浦肯野细胞、小脑颗粒细胞和中间神经元的胞体上,以及浦肯野细胞的树突上。在海马中,结合位点定位于CA1-CA4区锥体细胞的胞体以及齿状回颗粒细胞的胞体上。连续竞争反应证实了小脑和CA1锥体细胞中结合的特异性,也提示了CA1和CA3锥体细胞之间结合亲和力的差异。由于本研究需要高浓度的ω-阿加毒素IVA(2 microM),本研究中呈现的ω-阿加毒素IVA结合位点可能代表“P型”和“Q型”钙通道。