Pan Ping-Yue, Marrs Julia, Ryan Timothy A
From the Department of Biochemistry, Weill Cornell Medical College, New York, New York 10021.
From the Department of Biochemistry, Weill Cornell Medical College, New York, New York 10021
J Biol Chem. 2015 Sep 11;290(37):22593-601. doi: 10.1074/jbc.M115.651711. Epub 2015 Jul 29.
A long standing question in synaptic physiology is how neurotransmitter-filled vesicles are rebuilt after exocytosis. Among the first steps in this process is the endocytic retrieval of the transmembrane proteins that are enriched in synaptic vesicles (SVs). At least six types of transmembrane proteins must be recovered, but the rules for how this multiple cargo selection is accomplished are poorly understood. Among these SV cargos is the vesicular glutamate transporter (vGlut). We show here that vGlut1 has a strong influence on the kinetics of retrieval of half of the known SV cargos and that specifically impairing the endocytosis of vGlut1 in turn slows down other SV cargos, demonstrating that cargo retrieval is a collective cargo-driven process. Finally, we demonstrate that different cargos can be retrieved in the same synapse with different kinetics, suggesting that additional post-endocytic sorting steps likely occur in the nerve terminal.
突触生理学中一个长期存在的问题是,神经递质填充的囊泡在胞吐作用后如何重新构建。这一过程的首要步骤之一是对富含突触小泡(SVs)的跨膜蛋白进行内吞回收。至少六种类型的跨膜蛋白必须被回收,但对于如何完成这种多种货物选择的规则却知之甚少。在这些SV货物中有一种是囊泡谷氨酸转运体(vGlut)。我们在此表明,vGlut1对已知SV货物中一半的回收动力学有强烈影响,并且特异性地损害vGlut1的内吞作用反过来会减缓其他SV货物的回收,这表明货物回收是一个由货物驱动的集体过程。最后,我们证明不同的货物可以在同一突触中以不同的动力学被回收,这表明在神经末梢可能会发生额外的内吞后分选步骤。