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体外活动依赖性皮质脊髓突触消除的关键时期。

Critical period for activity-dependent elimination of corticospinal synapses in vitro.

作者信息

Ohno T, Sakurai M

机构信息

Department of Physiology, Teikyo University School of Medicine, Itabashi-ku, Tokyo, Japan.

出版信息

Neuroscience. 2005;132(4):917-22. doi: 10.1016/j.neuroscience.2005.01.056.

Abstract

There is no in vitro model of the critical periods for developmental plasticity, the time windows of plastic changes during development, which may hinder in-depth mechanistic analysis. We have shown previously that the corticospinal tract with synaptic connections can be reconstructed in in vitro co-cultures using slices of the sensorimotor cortex and spinal cord of the rat. In our in vitro system, corticospinal synapses form widely over spinal gray matter during early development, after which those on the ventral side are eliminated in an activity and N-methyl-D-aspartate (NMDA)-dependent manner. A detailed quantitative analysis of the time course of sensitivity to an NMDA blocker was made with this system. Synapse distribution was evaluated by recording field excitatory post-synaptic potentials evoked by deep cortical layer stimulation. Corticospinal axon terminal distribution was examined by anterograde labeling with biocytin. We showed that the D-2-amino-5-phosphonovaleric acid (APV) effect is irreversible for at least the length of culture. When APV was removed from the medium before 6 days in vitro(DIV) or after 11 DIV, elimination of ventral synapses was not blocked. APV sensitivity showed a clearly defined time window. A 6-11 DIV application was necessary and sufficient for the full, irreversible block of synapse elimination. From 6-11 DIV, APV sensitivity seems to decrease gradually but not linearly. This system provides an in vitro model of critical periods for developmental plasticity of central synapses which up to now has not been available.

摘要

发育可塑性关键期(即发育过程中可塑性变化的时间窗口)不存在体外模型,这可能会阻碍深入的机制分析。我们之前已经表明,具有突触连接的皮质脊髓束可以在体外共培养物中使用大鼠感觉运动皮层和脊髓切片进行重建。在我们的体外系统中,皮质脊髓突触在早期发育过程中广泛形成于脊髓灰质上,之后腹侧的突触以一种依赖于活动和N-甲基-D-天冬氨酸(NMDA)的方式被消除。利用该系统对NMDA阻滞剂敏感性的时间进程进行了详细的定量分析。通过记录深层皮质层刺激诱发的场兴奋性突触后电位来评估突触分布。通过用生物素进行顺行标记来检查皮质脊髓轴突终末分布。我们表明,至少在培养期间,D-2-氨基-5-磷酸戊酸(APV)的作用是不可逆的。当在体外培养6天(DIV)之前或11 DIV之后从培养基中去除APV时,腹侧突触的消除并未被阻断。APV敏感性显示出一个明确界定的时间窗口。6-11 DIV的应用对于完全、不可逆地阻断突触消除是必要且充分的。从6-11 DIV,APV敏感性似乎逐渐但非线性地降低。该系统提供了一个迄今为止尚未有的中枢突触发育可塑性关键期的体外模型。

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