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Plekhg5调控的突触小泡自噬揭示了运动神经元疾病的一种致病机制。

Plekhg5-regulated autophagy of synaptic vesicles reveals a pathogenic mechanism in motoneuron disease.

作者信息

Lüningschrör Patrick, Binotti Beyenech, Dombert Benjamin, Heimann Peter, Perez-Lara Angel, Slotta Carsten, Thau-Habermann Nadine, R von Collenberg Cora, Karl Franziska, Damme Markus, Horowitz Arie, Maystadt Isabelle, Füchtbauer Annette, Füchtbauer Ernst-Martin, Jablonka Sibylle, Blum Robert, Üçeyler Nurcan, Petri Susanne, Kaltschmidt Barbara, Jahn Reinhard, Kaltschmidt Christian, Sendtner Michael

机构信息

Institute of Clinical Neurobiology, University Hospital Würzburg, 97078, Würzburg, Germany.

Department of Cell Biology, University of Bielefeld, 33501, Bielefeld, Germany.

出版信息

Nat Commun. 2017 Oct 30;8(1):678. doi: 10.1038/s41467-017-00689-z.

Abstract

Autophagy-mediated degradation of synaptic components maintains synaptic homeostasis but also constitutes a mechanism of neurodegeneration. It is unclear how autophagy of synaptic vesicles and components of presynaptic active zones is regulated. Here, we show that Pleckstrin homology containing family member 5 (Plekhg5) modulates autophagy of synaptic vesicles in axon terminals of motoneurons via its function as a guanine exchange factor for Rab26, a small GTPase that specifically directs synaptic vesicles to preautophagosomal structures. Plekhg5 gene inactivation in mice results in a late-onset motoneuron disease, characterized by degeneration of axon terminals. Plekhg5-depleted cultured motoneurons show defective axon growth and impaired autophagy of synaptic vesicles, which can be rescued by constitutively active Rab26. These findings define a mechanism for regulating autophagy in neurons that specifically targets synaptic vesicles. Disruption of this mechanism may contribute to the pathophysiology of several forms of motoneuron disease.

摘要

自噬介导的突触成分降解维持突触稳态,但也构成神经退行性变的一种机制。目前尚不清楚突触小泡和突触前活动区成分的自噬是如何被调控的。在此,我们表明含普列克底物蛋白同源结构域家族成员5(Plekhg5)通过其作为小GTP酶Rab26的鸟嘌呤交换因子的功能,调节运动神经元轴突终末中突触小泡的自噬,Rab26特异性地将突触小泡导向自噬前体结构。小鼠中Plekhg5基因失活导致迟发性运动神经元疾病,其特征为轴突终末退化。Plekhg5缺失的培养运动神经元表现出轴突生长缺陷和突触小泡自噬受损,而组成型活性Rab26可挽救这些缺陷。这些发现定义了一种在神经元中调节自噬的机制,该机制特异性地靶向突触小泡。这种机制的破坏可能导致几种形式的运动神经元疾病的病理生理学改变。

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