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Calcineurin Aγ is a Functional Phosphatase That Modulates Synaptic Vesicle Endocytosis

机译:钙调磷酸酶Aγ是一种功能性磷酸酶可调节突触囊泡的内吞作用。

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摘要

Variation in PPP3CC, the gene that encodes the γ isoform of the calcineurin catalytic subunit, has been reported to be associated with schizophrenia. Because of its low expression level in most tissues, there has been little research devoted to the specific function of the calcineurin Aγ (CNAγ) versus the calcineurin Aα (CNAα) and calcineurin Aβ (CNAβ) catalytic isoforms. Consequently, we have a limited understanding of the role of altered CNAγ function in psychiatric disease. In this study, we demonstrate that CNAγ is present in the rodent and human brain and dephosphorylates a presynaptic substrate of calcineurin. Through a combination of immunocytochemistry and immuno-EM, we further show that CNAγ is localized to presynaptic terminals in hippocampal neurons. Critically, we demonstrate that RNAi-mediated knockdown of CNAγ leads to a disruption of synaptic vesicle cycling in cultured rat hippocampal neurons. These data indicate that CNAγ regulates a critical aspect of synaptic vesicle cycling and suggest that variation in PPP3CC may contribute to psychiatric disease by altering presynaptic function.
机译:据报道,编码钙调神经磷酸酶催化亚基的γ同工型的基因PPP3CC的变异与精神分裂症有关。由于其在大多数组织中的低表达水平,关于钙调神经磷酸酶Aγ(CNAγ)与钙调神经磷酸酶Aα(CNAα)和钙调神经磷酸酶Aβ(CNAβ)催化同工型的特定功能的研究很少。因此,我们对改变的CNAγ功能在精神疾病中的作用了解有限。在这项研究中,我们证明了啮齿动物和人脑中存在CNAγ,并且使钙调神经磷酸酶的突触前底物脱磷酸。通过免疫细胞化学和免疫EM的组合,我们进一步表明CNAγ定位于海马神经元的突触前终端。至关重要的是,我们证明RNAi介导的CNAγ的敲低导致培养的大鼠海马神经元中突触小泡循环的破坏。这些数据表明CNAγ调节突触小泡循环的关键方面,并表明PPP3CC的变化可能通过改变突触前功能而导致精神病。

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