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布雷菲德菌素A敏感机制有助于小脑颗粒细胞的内吞膜回收和囊泡循环利用。

Brefeldin A sensitive mechanisms contribute to endocytotic membrane retrieval and vesicle recycling in cerebellar granule cells.

作者信息

Rampérez Alberto, Sánchez-Prieto José, Torres Magdalena

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Veterinaria, Universidad Complutense, Madrid, Spain.

Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain.

出版信息

J Neurochem. 2017 Jun;141(5):662-675. doi: 10.1111/jnc.14017. Epub 2017 Apr 6.

Abstract

The recycling of synaptic vesicle (SV) proteins and transmitter release occur at multiple sites along the axon. These processes are sensitive to inhibition of the small GTP binding protein ARF1, which regulates the adaptor protein 1 and 3 complex (AP-1/AP-3). As the axon matures, SV recycling becomes restricted to the presynaptic bouton, and its machinery undergoes a complex process of maturation. We used the styryl dye FM1-43 to highlight differences in the efficiency of membrane recycling at different sites in cerebellar granule cells cultured for 7 days in vitro. We used Brefeldin A (BFA) to inhibit AP-1/AP-3-mediated recycling and to test the contribution of this pathway to the heterogeneity of the responses when these cells are strongly stimulated. Combining imaging techniques and ultrastructural analyses, we found a significant decrease in the density of functional boutons and an increase in the presence of endosome-like structures within the boutons of cells incubated with BFA prior to FM1-43 loading. Such effects were not observed when BFA was added 5 min after the end of the loading step, when endocytosis was almost fully completed. In this situation, vesicles were found closer to the active zone (AZ) in boutons exposed to BFA. Together, these data suggest that the AP-1/AP-3 pathway contributes to SV recycling, affecting different steps in all boutons but not equally, and thus being partly responsible for the heterogeneity of the different recycling efficiencies. Cover Image for this issue: doi. 10.1111/jnc.13801.

摘要

突触小泡(SV)蛋白的循环利用和神经递质释放发生在轴突沿线的多个位点。这些过程对小GTP结合蛋白ARF1的抑制敏感,ARF1调节衔接蛋白1和3复合物(AP-1/AP-3)。随着轴突成熟,SV循环利用局限于突触前终扣,其机制经历一个复杂的成熟过程。我们使用苯乙烯基染料FM1-43来突出体外培养7天的小脑颗粒细胞中不同位点膜循环利用效率的差异。我们使用布雷菲德菌素A(BFA)抑制AP-1/AP-3介导的循环利用,并测试该途径对这些细胞受到强烈刺激时反应异质性的贡献。结合成像技术和超微结构分析,我们发现在FM1-43加载前用BFA处理的细胞的终扣中,功能性终扣的密度显著降低,且终扣内类似内体结构的存在增加。当在加载步骤结束后5分钟添加BFA时,未观察到此类效应,此时内吞作用几乎完全完成。在这种情况下,在暴露于BFA的终扣中发现囊泡更靠近活性区(AZ)。总之,这些数据表明AP-1/AP-3途径有助于SV循环利用,影响所有终扣中的不同步骤,但程度不同,因此部分导致了不同循环利用效率的异质性。本期封面图片:doi. 10.1111/jnc.13801。

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