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大鼠海马器官型培养物中CA3锥体神经元向齿状回的发芽。

Sprouting of CA3 pyramidal neurons to the dentate gyrus in rat hippocampal organotypic cultures.

作者信息

Sakaguchi T, Okada M, Kawasaki K

机构信息

Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.

出版信息

Neurosci Res. 1994 Aug;20(2):157-64. doi: 10.1016/0168-0102(94)90033-7.

DOI:10.1016/0168-0102(94)90033-7
PMID:7808698
Abstract

The understanding of the mechanisms of a functional synaptic plasticity in the hippocampus has been expanded greatly by the use of in vitro slice preparations. The question addressed in the present study was whether morphological plasticity observed in vivo can also be reproduced in hippocampal slices. In vivo, hippocampal commissural and association fibers are known to sprout and occupy synaptic sites vacated by deafferentation of the dentate gyrus (DG). In hippocampal slice preparations, the major input to the DG is eliminated, so that the DG is deafferented. Might intrinsic neurons sprout to the DG if the slice preparation is maintained for weeks? In this study hippocampal slices obtained from 6-day-old rats were cultured. Stimulation of the dentate stratum moleculare produced antidromic field potentials in the CA3 of the slices cultivated for more than 1 week. The antidromic response was not observed in CA1 pyramidal neurons. The CA3 to DG projection response was also observed in a CA3 mini-slice placed near a co-cultured whole hippocampal slice, when the DG in the latter was stimulated. Moreover, stimulation of the CA3 mini-slice induced synaptic responses in the DG of the whole-slice. The conclusion drawn is that deafferentation could induce axonal sprouting in a neuron-specific manner in hippocampal organotypic culture. This preparation would be potentially useful for the screening of chemical factors that influence sprouting of central neurons.

摘要

通过使用体外脑片制备技术,人们对海马体中功能性突触可塑性机制的理解有了极大的扩展。本研究探讨的问题是,体内观察到的形态可塑性是否也能在海马体脑片中重现。在体内,已知海马连合纤维和联合纤维会发芽并占据齿状回(DG)去传入后空出的突触位点。在海马体脑片制备中,DG的主要输入被消除,从而使DG去传入。如果将脑片制备物维持数周,内在神经元会向DG发芽吗?在本研究中,培养了从6日龄大鼠获得的海马体脑片。刺激齿状分子层在培养超过1周的脑片的CA3区产生了逆向场电位。在CA1锥体神经元中未观察到逆向反应。当刺激共培养的完整海马体脑片中的DG时,在靠近其放置的CA3微型脑片中也观察到了CA3到DG的投射反应。此外,刺激CA3微型脑片可在完整脑片的DG中诱导突触反应。得出的结论是,去传入可以在海马体器官型培养中以神经元特异性方式诱导轴突发芽。这种制备方法可能对筛选影响中枢神经元发芽的化学因子有用。

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