Wu L G, Westenbroek R E, Borst J G, Catterall W A, Sakmann B
Abteilung Zellphysiologie, Max-Planck-Institut für medizinische Forschung, D-69120 Heidelberg, Germany.
J Neurosci. 1999 Jan 15;19(2):726-36. doi: 10.1523/JNEUROSCI.19-02-00726.1999.
We studied how Ca2+ influx through different subtypes of Ca2+ channels couples to release at a calyx-type terminal in the rat medial nucleus of the trapezoid body by simultaneously measuring the presynaptic Ca2+ influx evoked by a single action potential and the EPSC. Application of subtype-specific toxins showed that Ca2+ channels of the P/Q-, N-, and R-type controlled glutamate release at a single terminal. The Ca2+ influx through the P/Q-type channels triggered release more effectively than Ca2+ influx through N- or R-type channels. We investigated mechanisms that contributed to these differences in effectiveness. Electrophysiological experiments suggested that individual release sites were controlled by all three subtypes of Ca2+ channels. Immunocytochemical staining indicated, however, that a substantial fraction of N- and R-type channels was located distant from release sites. Although these distant channels contributed to the Ca2+ influx into the terminal, they may not contribute to release. Taken together, the results suggest that the Ca2+ influx into the calyx via N- and R-type channels triggers release less effectively than that via P/Q-type because a substantial fraction of the N- and R-type channels in the calyx is localized distant from release sites.
我们通过同时测量单个动作电位诱发的突触前Ca²⁺内流和兴奋性突触后电流(EPSC),研究了在大鼠梯形体内侧核的花萼型终末中,通过不同亚型Ca²⁺通道的Ca²⁺内流如何与递质释放相偶联。应用亚型特异性毒素表明,P/Q型、N型和R型Ca²⁺通道在单个终末控制谷氨酸释放。通过P/Q型通道的Ca²⁺内流比通过N型或R型通道的Ca²⁺内流更有效地触发释放。我们研究了导致这些有效性差异的机制。电生理实验表明,单个释放位点受所有三种Ca²⁺通道亚型的控制。然而,免疫细胞化学染色表明,相当一部分N型和R型通道位于远离释放位点的地方。虽然这些远处的通道对Ca²⁺流入终末有贡献,但它们可能对释放没有贡献。综上所述,结果表明,通过N型和R型通道进入花萼的Ca²⁺内流比通过P/Q型通道触发释放的效率更低,因为花萼中相当一部分N型和R型通道位于远离释放位点的地方。