首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Brefeldin A sensitive mechanisms contribute to endocytotic membrane retrieval and vesicle recycling in cerebellar granule cells
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Brefeldin A sensitive mechanisms contribute to endocytotic membrane retrieval and vesicle recycling in cerebellar granule cells

机译:Brefeldin敏感机制有助于内吞膜检索和囊泡在小脑颗粒细胞中回收

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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 ARF 1, 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 FM 1‐43 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 FM 1‐43 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 .
机译:摘要突触囊泡(SV)蛋白和发射器释放的再循环发生在沿着轴突的多个位点。这些方法对小GTP结合蛋白ARF 1的抑制敏感,其调节适配器蛋白1和3络合物(AP -1 / AP -3)。随着轴突的成熟,SV回收变得限制在突触前Bouton,其机器经历复杂的成熟过程。我们使用Styryl染料FM1-43突出培养的小脑颗粒细胞在培养的小脑颗粒细胞中回收膜效率的差异。我们使用Brefeldin A(BFA)来抑制AP -1 / AP -3介导的再循环,并在强烈刺激这些细胞时测试该途径对响应的异质性的贡献。结合成像技术和超微结构分析,我们发现功能性Bouton的密度显着降低,并且在FM 1-43负载之前与BFA孵育的细胞的前型细胞内的内体状结构的存在增加。当加载步骤结束后加入5≤min时,未观察到这种效果,当前吞作用几乎完全完成时。在这种情况下,发现囊泡更接近暴露于BFA的前置件中的有源区(AZ)。这些数据表明,AP -1 / AP -3途径有助于SV回收,影响所有方位的不同步骤,但不同等地,因此部分地负责不同循环效率的异质性。封面图像为此问题:DOI。 10.1111 / JNC.13801。

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