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MUNC18-1的缺失导致神经元中的逆行运输缺陷。

Loss of MUNC18-1 leads to retrograde transport defects in neurons.

作者信息

van Berkel Annemiek A, Santos Tatiana C, Shaweis Hesho, van Weering Jan R T, Toonen Ruud F, Verhage Matthijs

机构信息

Department of Clinical Genetics, Center for Neurogenomics and Cognitive Research (CNCR), University Medical Center Amsterdam, Amsterdam, The Netherlands.

Department of Functional Genomics, Center for Neurogenomics and Cognitive Research (CNCR), VU University Amsterdam, Amsterdam, The Netherlands.

出版信息

J Neurochem. 2021 May;157(3):450-466. doi: 10.1111/jnc.15256. Epub 2020 Dec 12.

Abstract

Loss of the exocytic Sec1/MUNC18 protein MUNC18-1 or its target-SNARE partners SNAP25 and syntaxin-1 results in rapid, cell-autonomous and unexplained neurodegeneration, which is independent of their known role in synaptic vesicle exocytosis. cis-Golgi abnormalities are the earliest cellular phenotypes before degeneration occurs. Here, we investigated whether loss of MUNC18-1 causes defects in intracellular membrane transport pathways in primary murine neurons that may explain neurodegeneration. Electron, confocal and super resolution microscopy confirmed that loss of MUNC18-1 expression results in a smaller cis-Golgi. In addition, we now show that medial-Golgi and the trans-Golgi Network are also affected. However, stacking and cisternae ultrastructure of the Golgi were normal. Overall, ultrastructure of null mutant neurons was remarkably normal just hours before cell death occurred. By synchronizing protein trafficking by conditional cargo retention in the endoplasmic reticulum using selective hooks (RUSH) and immunocytochemistry, we show that anterograde Endoplasmic Reticulum-to-Golgi and Golgi exit of endogenous and exogenous proteins were normal. In contrast, loss of MUNC18-1 caused reduced retrograde Cholera Toxin B-subunit transport from the plasma membrane to the Golgi. In addition, MUNC18-1-deficiency resulted in abnormalities in retrograde TrkB trafficking in an antibody uptake assay. We conclude that MUNC18-1 deficient neurons have normal anterograde but reduced retrograde transport to the Golgi. The impairments in retrograde pathways suggest a role of MUNC18-1 in endosomal SNARE-dependent fusion and provide a plausible explanation for the observed Golgi abnormalities and cell death in MUNC18-1 deficient neurons.

摘要

胞吐作用的Sec1/MUNC18蛋白MUNC18-1或其靶标-SNARE伴侣SNAP25和 syntaxin-1的缺失会导致快速、细胞自主性且原因不明的神经退行性变,这与其在突触小泡胞吐作用中的已知功能无关。顺式高尔基体异常是变性发生前最早出现的细胞表型。在此,我们研究了MUNC18-1的缺失是否会导致原代小鼠神经元细胞内膜转运途径出现缺陷,这或许可以解释神经退行性变的原因。电子显微镜、共聚焦显微镜和超分辨率显微镜证实,MUNC18-1表达缺失会导致顺式高尔基体变小。此外,我们现在还表明,中间高尔基体和反式高尔基体网络也受到影响。然而,高尔基体的堆叠和潴泡超微结构是正常的。总体而言,在细胞死亡发生前数小时,无效突变神经元的超微结构显著正常。通过使用选择性钩子(RUSH)在内质网中通过条件性货物滞留来同步蛋白质运输以及免疫细胞化学方法,我们发现内源性和外源性蛋白质的顺行内质网到高尔基体运输以及高尔基体输出均正常。相比之下,MUNC18-1的缺失导致霍乱毒素B亚基从质膜到高尔基体的逆行运输减少。此外,在抗体摄取试验中,MUNC18-1缺陷导致逆行TrkB运输异常。我们得出结论,MUNC18-1缺陷的神经元具有正常的顺行运输,但逆行运输到高尔基体的过程减少。逆行途径的损伤表明MUNC18-1在内体SNARE依赖性融合中发挥作用,并为MUNC18-1缺陷神经元中观察到的高尔基体异常和细胞死亡提供了合理的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e66c/8247427/aff47e0f8fbe/JNC-157-450-g004.jpg

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