首页> 美国卫生研究院文献>Frontiers in Synaptic Neuroscience >The Shank3 Interaction Partner ProSAPiP1 Regulates Postsynaptic SPAR Levels and the Maturation of Dendritic Spines in Hippocampal Neurons
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The Shank3 Interaction Partner ProSAPiP1 Regulates Postsynaptic SPAR Levels and the Maturation of Dendritic Spines in Hippocampal Neurons

机译:Shank3相互作用伙伴ProSAPiP1调节突触后SPAR水平和海马神经元中树突棘的成熟。

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摘要

The postsynaptic density or PSD is a submembranous compartment containing a wide array of proteins that contribute to both morphology and function of excitatory glutamatergic synapses. In this study, we have analyzed functional aspects of the Fezzin ProSAP-interacting protein 1 (ProSAPiP1), an interaction partner of the well-known PSD proteins Shank3 and SPAR. Using lentiviral-mediated overexpression and knockdown of ProSAPiP1, we found that this protein is dispensable for the formation of both pre- and postsynaptic specializations per se. We further show that ProSAPiP1 regulates SPAR levels at the PSD and the maturation of dendritic spines. In line with previous findings on the ProSAPiP1 homolog PSD-Zip70, we conclude that Fezzins essentially contribute to the maturation of excitatory spine synapses.
机译:突触后密度或PSD是一个膜下隔室,其中包含多种蛋白质,这些蛋白质有助于形态学和兴奋性谷氨酸能突触的功能。在这项研究中,我们分析了Fezzin ProSAP相互作用蛋白1(ProSAPiP1)的功能方面,Prozzi ProSAPiP1是著名的PSD蛋白Shank3和SPAR的相互作用伴侣。使用慢病毒介导的ProSAPiP1的过表达和敲低,我们发现该蛋白对于突触前和突触后专业化本身的形成都是必不可少的。我们进一步表明ProSAPiP1调节PSD和树突棘成熟的SPAR水平。与以前对ProSAPiP1同源PSD-Zip70的发现相一致,我们得出结论,Fezzins实质上有助于兴奋性脊柱突触的成熟。

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