Lichtenstein Y, Desnos C, Faúndez V, Kelly R B, Clift-O'Grady L
Department of Biochemistry and Biophysics and Hormone Research Institute, University of California, San Francisco, CA 94143-0534, USA.
Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11223-8. doi: 10.1073/pnas.95.19.11223.
Formation of small vesicles resembling synaptic vesicles can be reconstituted in vitro by incubating labeled homogenates of PC12 cells with ATP and two cytoplasmic proteins, AP3 and ARF1 [Faúndez, V., Horng, J.-T. & Kelly, R. B. (1998) Cell 93, 423-432]. To determine whether AP3 was mediating budding from plasma membranes or endosomes the organelle that generated the synaptic vesicles was characterized. The budding activity was enriched in organelles that labeled at 15 degrees C, but not at 4 degrees C, that excluded a marker of plasma membranes and that contained internalized transferrin, indicating that the precursor was an endosome. Vesicles formed from the endosomal precursor in vitro excluded transferrin. We conclude that ARF-mediated vesiculation into synaptic vesicle-sized organelles uses an endosomal precursor and occurs simultaneously in vitro with sorting of synaptic vesicle proteins from other membrane protein constituents of the endosome.
通过将PC12细胞的标记匀浆与ATP以及两种细胞质蛋白AP3和ARF1一起孵育,可在体外重建类似突触小泡的小泡形成过程[法恩德兹,V.,洪,J.-T.和凯利,R.B.(1998年)《细胞》93卷,423 - 432页]。为了确定AP3是介导从质膜还是内体出芽,对产生突触小泡的细胞器进行了表征。出芽活性在15℃标记但4℃不标记的细胞器中富集,这些细胞器排除了质膜标记物且含有内化的转铁蛋白,表明前体是内体。体外由内体前体形成的小泡排除了转铁蛋白。我们得出结论,ARF介导的形成突触小泡大小细胞器的囊泡化过程利用内体前体,并且在体外与从内体的其他膜蛋白成分中分拣突触小泡蛋白同时发生。