Aim 1 Classical neuroscience has proposed two competing models for membrane fusion. In the first, vesicles completely merge with the plasma membrane, dispersing the entirety of their contents. This full fusion model of exocytosis predicts that vesicle contents will spill into the membrane and diffuse away from the site of fusion. In the second, vesicles transiently connect with the plasma membrane and release only a subset of their components. This kiss-and-run model predicts that the vesicle contents will remain within a vesicle cavity and then will be recaptured into the cell mostly intact. To determine which of these two models occurs in neuroendocrine cells, we have imaged single fluorescently-tagged vesicles in living PC12 cells with total internal reflection fluorescent microscopy (TIRF). This method allows us to track and measure the behavior of individual secretory vesicles in real time in living cells. By watching the diffusive behavior of vesicle components before, during, and after fusion, we will determine if (or which of) the two classical models of fusion fit triggered exocytosis of vesicles in PC12 cells. Through these studies we hope to measure the behavior of individual vesicles to determine the heterogeneity of vesicle fusion behaviors, their topology, relationships, and regulation by cellular signaling pathway and pathologies. Using two-color total internal reflection microscopy we have shown that the dominant mode of fusion for SLMV in PC12 cells is the full fusion model. As such, vesicle transporters, including the vesicular acetylcholine transporter, diffuse into the plasma membrane within seconds. A surprising finding of this work, however, is that the material that exits vesicles is rapidly captured on preformed clusters on the cells surface. These clusters composed of the endocytic protein clathrin and other proteins involved in endocytosis inhibit the free diffusion of the transporter across the plasma membrane. To further investigate the density and topology of the structures responsible for capturing VAChT on the cell surface, we used three forms of ultra-high resolution imaging: 1) photo-activation localization microscopy, 2) ground state depletion (GSD) super-resolution imaging, and 2) electron microscopy. The combinations of these methods have shown that the density of endocytic clathrin-coated structures in PC12 cells is very high. The density approaches 2 structures per square micron. The structures are randomly distributed across the surface of the cell, and produce a network of endocytic nano-traps capable of rapidly capturing material that escapes from exocytic vesicles. We propose that this system can account for the rapidly recycling of vesicle material in highly excitable cells necessary for the continued function of the nervous and neuroendocrine system.
Aim 2 Dozens of proteins control the docking, fusion, and then recapture of vesicles in excitable cells. The identity and functional roles of many of these proteins have been discovered through a combination of genetics, biochemistry, and electrophysiology. However, the architecture, structure, and structural dynamics of these proteins and their complexes have yet to be determined. In this aim we have maped the location, architecture, and dynamics of proteins proposed to act during exocytosis and endocytosis. To accomplish this, we are using a combination of live cell imaging, super-resolution, and electron microscopy. Through this multi-modal approach, the location, and dynamics of individual proteins are being compared to the underlying cellular architecture that organizes exocytic and endocytic sites at the nanometer scale. This allows us to map the architecture of the plasma membrane along with protein components responsible for vesicle trafficking. These studies are determining the complex three dimensional structure of the exocytic and endocytic protein machinery in intact cells. We have been using two-color TIRF microscopy and a form of high-throughput image analysis to detect and characterize over 70 proteins that are associated with endocytic and exocytic vesicles. These studies have rapidly mapped the occupancy and distribution of these proteins at the plasma membrane. Our studies are developing a general topographic map of the endocytic and exocytic machinery in living neuroendocrine cells at the plasma membrane. These studies will provide a systems level network analysis of the machinery responsible for vesicle fusion and recapture in cells of the nervous system.

Project Start
Project End
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Budget End
Support Year
3
Fiscal Year
2013
Total Cost
$974,435
Indirect Cost
Name
National Heart, Lung, and Blood Institute
Department
Type
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Bucher, Delia; Frey, Felix; Sochacki, Kem A et al. (2018) Clathrin-adaptor ratio and membrane tension regulate the flat-to-curved transition of the clathrin coat during endocytosis. Nat Commun 9:1109
Somasundaram, Agila; Taraska, Justin W (2018) Local protein dynamics during microvesicle exocytosis in neuroendocrine cells. Mol Biol Cell 29:1891-1903
Dambournet, Daphné; Sochacki, Kem A; Cheng, Aaron T et al. (2018) Genome-edited human stem cells expressing fluorescently labeled endocytic markers allow quantitative analysis of clathrin-mediated endocytosis during differentiation. J Cell Biol 217:3301-3311
Kong, Leopold; Sochacki, Kem A; Wang, Huaibin et al. (2018) Cryo-EM of the dynamin polymer assembled on lipid membrane. Nature 560:258-262
Scott, Brandon L; Sochacki, Kem A; Low-Nam, Shalini T et al. (2018) Membrane bending occurs at all stages of clathrin-coat assembly and defines endocytic dynamics. Nat Commun 9:419
Guo, Min; Chandris, Panagiotis; Giannini, John Paul et al. (2018) Single-shot super-resolution total internal reflection fluorescence microscopy. Nat Methods :
Trexler, Adam J; Taraska, Justin W (2017) Regulation of insulin exocytosis by calcium-dependent protein kinase C in beta cells. Cell Calcium 67:1-10
Sochacki, Kem A; Dickey, Andrea M; Strub, Marie-Paule et al. (2017) Endocytic proteins are partitioned at the edge of the clathrin lattice in mammalian cells. Nat Cell Biol 19:352-361
Martineau, Magalie; Somasundaram, Agila; Grimm, Jonathan B et al. (2017) Semisynthetic fluorescent pH sensors for imaging exocytosis and endocytosis. Nat Commun 8:1412
Trexler, Adam J; Taraska, Justin W (2017) Two-Color Total Internal Reflection Fluorescence Microscopy of Exocytosis in Endocrine Cells. Methods Mol Biol 1563:151-165

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