Nabekura Junichi, Katsurabayashi Shutaro, Kakazu Yasuhiro, Shibata Shumei, Matsubara Atsushi, Jinno Shozo, Mizoguchi Yoshito, Sasaki Akira, Ishibashi Hitoshi
Department of Cellular and System Physiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Nat Neurosci. 2004 Jan;7(1):17-23. doi: 10.1038/nn1170. Epub 2003 Dec 21.
Early in postnatal development, inhibitory inputs to rat lateral superior olive (LSO) neurons change from releasing predominantly GABA to releasing predominantly glycine into the synapse. Here we show that spontaneous miniature inhibitory postsynaptic currents (mIPSCs) also change from GABAergic to glycinergic over the first two postnatal weeks. Many 'mixed' mIPSCs, resulting from co-release of glycine and GABA from the same vesicles, are seen during this transition. Immunohistochemistry showed that a large number of terminals contained both GABA and glycine at postnatal day 8 (P8). By P14, both the content of GABA in these mixed terminals and the contribution of GABA to the mixed mIPSCs had decreased. The content of glycine in terminals increased over the same period. Our results indicate that switching from GABAergic to glycinergic inputs to the LSO may occur at the level of a single presynaptic terminal. This demonstrates a new form of developmental plasticity at the level of a single central synapse.
在出生后早期发育阶段,大鼠外侧上橄榄核(LSO)神经元的抑制性输入从主要释放γ-氨基丁酸(GABA)转变为主要释放甘氨酸到突触中。在此我们表明,在出生后的前两周内,自发微小抑制性突触后电流(mIPSCs)也从GABA能转变为甘氨酸能。在这个转变过程中,可以看到许多由同一囊泡共同释放甘氨酸和GABA所导致的“混合”mIPSCs。免疫组织化学显示,在出生后第8天(P8),大量终末同时含有GABA和甘氨酸。到出生后第14天(P14),这些混合终末中GABA的含量以及GABA对混合mIPSCs的贡献都下降了。同期终末中甘氨酸的含量增加。我们的结果表明,LSO从GABA能输入到甘氨酸能输入的转变可能发生在单个突触前终末水平。这证明了单个中枢突触水平上一种新的发育可塑性形式。