Assembly of presynaptic active zones from cytoplasmic transport packets

Little is known about presynaptic assembly during central nervous system synaptogenesis. Here we used time-lapse fluorescence imaging, immunocytochemistry and electron microscopy to study hippocampal neuronal cultures transfected with a fusion construct of the presynaptic vesicle protein VAMP and green fluorescent protein. Our results suggest that major cytoplasmic and membrane-associated protein precursors of the presynaptic active zone are transported along developing axons together as discrete packets. Retrospective electron microscopy demonstrated varied vesicular and tubulovesicular membrane structures. Packets containing these heterogeneous structures were stabilized specifically at new sites of dendrite- and axon-initiated cell–cell contact; within less than one hour, evoked vesicle recycling was observed at these putative nascent synapses. These observations suggest that substantial membrane remodeling may be necessary to produce the uniform vesicles typical of the mature active zone, and that many presynaptic proteins may be united early in their biogenesis and sorting pathways.

[1]  Stephen J. Smith,et al.  The kinetics of synaptic vesicle recycling measured at single presynaptic boutons , 1993, Neuron.

[2]  R. Tsien,et al.  Properties of synaptic transmission at single hippocampal synaptic boutons , 1995, Nature.

[3]  Gero Miesenböck,et al.  Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins , 1998, Nature.

[4]  A. D. Blagoveshchenskaya,et al.  Secretagogue-triggered transfer of membrane proteins from neuroendocrine secretory granules to synaptic-like microvesicles. , 1999, Molecular biology of the cell.

[5]  R. Kelly,et al.  Endocrine secretory granules and neuronal synaptic vesicles have three integral membrane proteins in common , 1988, The Journal of cell biology.

[6]  R. Kelly,et al.  A v-SNARE participates in synaptic vesicle formation mediated by the AP3 adaptor complex , 1998, Nature Neuroscience.

[7]  Stephen J. Smith,et al.  Optical detection of a quantal presynaptic membrane turnover , 1997, Nature.

[8]  J. Buchanan,et al.  Studies of nerve-muscle interactions in Xenopus cell culture: fine structure of early functional contacts , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  P. De Camilli,et al.  Synaptogenesis in hippocampal cultures: evidence indicating that axons and dendrites become competent to form synapses at different stages of neuronal development , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  J. E. Vaughn,et al.  Fine structure of synaptogenesis in the vertebrate central nervous system. , 1989, Synapse.

[11]  P. De Camilli,et al.  Exo-endocytotic recycling of synaptic vesicles in developing processes of cultured hippocampal neurons , 1992, The Journal of cell biology.

[12]  H. Ishikawa,et al.  The movement of membranous organelles in axons. Electron microscopic identification of anterogradely and retrogradely transported organelles , 1980, The Journal of cell biology.

[13]  G. Banker,et al.  An electron microscopic study of the development of axons and dendrites by hippocampal neurons in culture. I. Cells which develop without intercellular contacts , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  B. Wiedenmann,et al.  Immunoelectron microscopic localization of synaptophysin in a golgi subcompartment of developing hypothalamic neurons , 1988, Neuroscience.

[15]  James E. Vaughn,et al.  Review: Fine structure of synaptogenesis in the vertebrate central nervous system , 1989 .

[16]  Stephen J. Smith,et al.  Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation , 1996, Neuron.

[17]  H. Aberle,et al.  Cadherin‐catenin complex: Protein interactions and their implications for cadherin function , 1996, Journal of cellular biochemistry.

[18]  G. Banker,et al.  Culturing nerve cells , 1998 .

[19]  W. Huttner,et al.  Newly synthesized synaptophysin is transported to synaptic‐like microvesicles via constitutive secretory vesicles and the plasma membrane. , 1991, The EMBO journal.

[20]  Stephen J. Smith Dissecting Dendrite Dynamics , 1999, Science.

[21]  N. Hirokawa,et al.  Visualization of the Dynamics of Synaptic Vesicle and Plasma Membrane Proteins in Living Axons , 1998, The Journal of cell biology.

[22]  E. Holtzman The origin and fate of secretory packages, especially synaptic vesicles , 1977, Neuroscience.

[23]  P. Greengard,et al.  Kinetic analysis of the phosphorylation‐dependent interactions of synapsin I with rat brain synaptic vesicles , 1997, The Journal of physiology.

[24]  W. Volknandt,et al.  Intraneuronal distribution of a synaptic vesicle membrane protein: Antibody binding sites at axonal membrane compartments andtrans-Golgi network and accumulation at nodes of Ranvier , 1989, Neuroscience.

[25]  Y. Goda,et al.  Synaptic Adhesion: the Building Blocks of Memory? , 1998, Neuron.

[26]  M. Greenberg,et al.  Calcium Influx via the NMDA Receptor Induces Immediate Early Gene Transcription by a MAP Kinase/ERK-Dependent Mechanism , 1996, The Journal of Neuroscience.

[27]  H. Winkler,et al.  The Life Cycle of Catecholamine‐storing Vesicles a , 1987, Annals of the New York Academy of Sciences.

[28]  E. Papini,et al.  Vesicle-associated Membrane Protein (VAMP)/Synaptobrevin-2 Is Associated with Dense Core Secretory Granules in PC12 Neuroendocrine Cells (*) , 1995, The Journal of Biological Chemistry.

[29]  P. De Camilli,et al.  Synaptic vesicle dynamics in living cultured hippocampal neurons visualized with CY3-conjugated antibodies directed against the lumenal domain of synaptotagmin , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  D. Colman Neurites, Synapses, and Cadherins Reconciled , 1997, Molecular and Cellular Neuroscience.

[31]  B. Gumbiner,et al.  Cell Adhesion: The Molecular Basis of Tissue Architecture and Morphogenesis , 1996, Cell.