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Developmental changes in presynaptic calcium channels coupled to glutamate release in cultured rat hippocampal neurons

机译:突触前钙通道的发育变化与培养的大鼠海马神经元中谷氨酸的释放相关

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摘要

Excitatory synaptic transmission in the hippocampus involves the participation of at least two types of presynaptic Ca2+ channels, N- type channels sensitive to omega-conotoxin GVIA (omega-CTx GVIA) and Q- type channels sensitive to omega-agatoxin IVA (omega-Aga IVA). Hippocampal pyramidal neurons in cell culture were used to examine the participation of these two classes of channels at different stages of synapse development. Specific Ca2+ channel toxins were used to block presynaptic Ca2+ channels while whole-cell voltage-clamp recordings were used to record evoked EPSCs in postsynaptic neurons. At immature synapses (cells in culture for 10–15 d), omega-CTx GVIA (1–5 microM) blocked transmission by more than 80% while omega-Aga IVA (1 microM) was less effective. In older cultures, however, omega-Aga IVA (1 microM) was more effective than omega-CTx GVIA (1–5 microM) in blocking synaptic transmission. The pharmacological properties of the omega-Aga IVA sensitive component of synaptic transmission were examined in more detail using omega-Aga IVA and omega-conotoxin MVIIC (omega-CTx MVIIC). The properties of this component of transmitter release indicated that a Q-type Ca2+ channel was involved in presynaptic Ca2+ entry. The results suggest that different classes of presynaptic Ca2+ channels begin to participate in transmitter release at different times during synapse development and maturation.
机译:海马兴奋性突触传递涉及至少两种类型的突触前Ca2 +通道的参与:对ω-芋螺毒素GVIA(omega-CTx GVIA)敏感的N型通道和对ω-藻毒素IVA(omega-Aga)敏感的Q型通道的参与IVA)。细胞培养中的海马锥体神经元用于检查突触发育不同阶段的这两类通道的参与。特定的Ca2 +通道毒素用于阻断突触前的Ca2 +通道,而全细胞电压钳记录则用于记录突触后神经元中诱发的EPSC。在未成熟的突触中(培养10–15 d的细胞),omega-CTx GVIA(1-5 microM)阻止了80%以上的传播,而omega-Aga IVA(1 microM)效果较差。然而,在较老的文化中,omega-Aga IVA(1 microM)在阻止突触传递方面比omega-CTx GVIA(1-5 microM)更有效。使用omega-Aga IVA和omega-conotoxin MVIIC(omega-CTx MVIIC)更详细地检查了Omega-Aga IVA突触传递敏感成分的药理特性。递质释放的这一成分的特性表明,突触前Ca2 +进入涉及Q型Ca2 +通道。结果表明,不同种类的突触前Ca2 +通道在突触形成和成熟过程中的不同时间开始参与递质的释放。

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