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反复激活蛋白激酶A后,培养的大鼠海马神经元中形成持久的突触。

Long-lasting synapse formation in cultured rat hippocampal neurons after repeated PKA activation.

作者信息

Yamamoto Megumi, Urakubo Tomoyoshi, Tominaga-Yoshino Keiko, Ogura Akihiko

机构信息

Osaka University Graduate School of Science, Toyonaka, Osaka 560-0043, Japan.

出版信息

Brain Res. 2005 Apr 25;1042(1):6-16. doi: 10.1016/j.brainres.2005.01.102.

Abstract

Recently, we reported that the repeated activation of cyclic-AMP-dependent protein kinase (PKA) in the rat hippocampus under tissue culture conditions induced the enhancement of excitatory postsynaptic potential (EPSP), which lasted more than 2 weeks and was accompanied by the formation of morphologically identifiable synapses. Here we examined whether an equivalent synapse formation is induced in dissociated cell cultures of rat hippocampal neurons. Brief (15-min) application of Sp-cAMPS (a membrane-permeable analog of cyclic AMP) induced an increase in the number of synaptic sites (identified by the apposition of immunocytochemically labeled pre- and postsynaptic structures). There were two types of increase: a short-lasting one that lasted less than 24 h after a single application of Sp-cAMPS, and a long-lasting one that lasted more than 2 weeks after repeated applications. The long-lasting increase in synaptic sites was dependent on the time and interval of application and was suppressed by Rp-cAMPS (a PKA inhibitor). The synapses were judged to be active based on the endocytosis of FM1-43, a fluorescent dye. Electron microscopy confirmed the increase in the number of synaptic ultrastructures. The present results show that the synaptogenesis induced by repeated PKA activation is reproducible in a neuronal network that is reconstituted under dissociated cell culture conditions. This experimental system, together with the synaptogenesis in the slice culture system described previously, serves as a good in vitro model for the analysis of the process of conversion from short-lasting plasticity (lasting for hours) into a long-lasting one (lasting for days-weeks).

摘要

最近,我们报道在组织培养条件下,大鼠海马体中环磷酸腺苷依赖性蛋白激酶(PKA)的反复激活会诱导兴奋性突触后电位(EPSP)增强,这种增强持续超过2周,并伴有形态可识别突触的形成。在此,我们研究了在大鼠海马神经元的解离细胞培养物中是否会诱导等效的突触形成。短暂(15分钟)应用Sp-cAMPS(环磷酸腺苷的膜渗透性类似物)会诱导突触位点数量增加(通过免疫细胞化学标记的突触前和突触后结构的并置来识别)。增加有两种类型:单次应用Sp-cAMPS后持续不到24小时的短期增加,以及反复应用后持续超过2周的长期增加。突触位点的长期增加取决于应用的时间和间隔,并被Rp-cAMPS(一种PKA抑制剂)抑制。根据荧光染料FM1-43的内吞作用判断突触是活跃的。电子显微镜证实了突触超微结构数量的增加。目前的结果表明,在解离细胞培养条件下重组的神经元网络中,由PKA反复激活诱导的突触形成是可重复的。这个实验系统,连同之前描述的切片培养系统中的突触形成,可作为一个很好的体外模型,用于分析从短期可塑性(持续数小时)转变为长期可塑性(持续数天至数周)的过程。

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