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Journal of Neuroscience, Vol 11, 1617-1626, Copyright © 1991 by Society for Neuroscience


ARTICLE

The distribution of synapsin I and synaptophysin in hippocampal neurons developing in culture

TL Fletcher, P Cameron, P De Camilli and G Banker
Department of Anatomy, Cell Biology, and Neurobiology, Albany Medical College, New York 12208.

As a first step toward elucidating mechanisms involved in the sorting of synaptic vesicle proteins in neurons, we have used immunofluorescence microscopy to determine the distribution of two synaptic vesicle proteins, synapsin I and synaptophysin, in hippocampal neurons developing in culture. In mature cultures, synapsin I and synaptophysin immunoreactivity was concentrated in puncta that were restricted to sites where axons contacted neuronal cell bodies or dendrites. Electron-microscopic immunocytochemistry demonstrated that these puncta corresponded to vesicle-filled axonal varicosities that were exclusively presynaptic. At early stages of development, before cell-cell contact, both synapsin I and synaptophysin were preferentially localized in axons, where they were particularly concentrated in the distal axon and growth cone. In axons that did not contact other cells, immunostaining for these two proteins had a granular appearance, which persisted for at least 7 d, but focal accumulations of vesicles comparable to those seen at sites of synaptic contact were not observed. When neurons contacted one another, numerous puncta of synapsin I and synaptophysin formed within the first week in culture. Double-label immunofluorescence demonstrated that the two vesicle antigens were closely codistributed throughout these stages of development. These observations demonstrate that synaptic vesicle proteins assume a polarized distribution within nerve cells beginning early in development, as soon as the axon can be identified. In contrast, differences in microtubule polarity orientation that distinguish mature axons and dendrites, and that have been proposed to account for the selective sorting of some materials in nerve cells, first appear at a subsequent stage of development. The selective distribution of synaptic vesicle proteins to the axon occurs in isolated cells, independent of interactions with other cells. In contrast, the formation of large clusters of vesicles typical of presynaptic specializations requires contact with an appropriate postsynaptic target. Thus, in cultured hippocampal neurons, the localization of synaptic vesicles in presynaptic specializations is the result of sorting mechanisms intrinsic to individual neurons as well as to mechanisms mediated by cell-cell contact.


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Activity-Independent Segregation of Excitatory and Inhibitory Synaptic Terminals in Cultured Hippocampal Neurons
J. Neurosci., October 15, 1996; 16(20): 6424 - 6432.
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J. Neurosci.Home page
P. Poisbeau, F. Rene, C. Egles, J.-M. Felix, P. Feltz, and R. Schlichter
Characterization of Functional GABAergic Synapses Formed between Rat Hypothalamic Neurons and Pituitary Intermediate Lobe Cells in Coculture: Ca2+ Dependence of Spontaneous IPSCs
J. Neurosci., August 15, 1996; 16(16): 4835 - 4845.
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J. Biol. Chem.Home page
K. Hirschberg, R. Zisling, G. van Echten-Deckert, and A. H. Futerman
Ganglioside Synthesis during the Development of Neuronal Polarity. MAJOR CHANGES OCCUR DURING AXONOGENESIS AND AXON ELONGATION, BUT NOT DURING DENDRITE GROWTH OR SYNAPTOGENESIS
J. Biol. Chem., June 21, 1996; 271(25): 14876 - 14882.
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J. Neurosci.Home page
A. M. Craig, G. Banker, W. Chang, M. E. McGrath, and A. S. Serpinskaya
Clustering of Gephyrin at GABAergic but Not Glutamatergic Synapses in Cultured Rat Hippocampal Neurons
J. Neurosci., May 15, 1996; 16(10): 3166 - 3177.
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J. Biol. Chem.Home page
J. Ahn, O. Mundigl, T. R. Muth, G. Rudnick, and M. J. Caplan
Polarized Expression of GABA Transporters in Madin-Darby Canine Kidney Cells and Cultured Hippocampal Neurons
J. Biol. Chem., March 22, 1996; 271(12): 6917 - 6924.
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J. Cell Sci.Home page
A Sofer, G Schwarzmann, and A. Futerman
The internalization of a short acyl chain analogue of ganglioside GM1 in polarized neurons
J. Cell Sci., January 8, 1996; 109(8): 2111 - 2119.
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J. Biol. Chem.Home page
A. Schwarz, E. Rapaport, K. Hirschberg, and A. H. Futerman
A Regulatory Role for Sphingolipids in Neuronal Growth
J. Biol. Chem., May 5, 1995; 270(18): 10990 - 10998.
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ScienceHome page
A Ferreira, K. Kosik, P Greengard, and H. Han
Aberrant neurites and synaptic vesicle protein deficiency in synapsin II-depleted neurons
Science, May 13, 1994; 264(5161): 977 - 979.
[Abstract] [PDF]


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ScienceHome page
Y. Shoji-Kasai, A. Yoshida, K. Sato, T. Hoshino, A. Ogura, S. Kondo, Y. Fujimoto, R. Kuwahara, R. Kato, and M. Takahashi
Neurotransmitter Release from Synaptotagmin-Deficient Clonal Variants of PC 12 Cells
Science, June 26, 1992; 256(5065): 1820 - 1823.
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Cold Spring Harb Symp Quant BiolHome page
M. Geppert, Y.A. Ushkaryov, Y. Hata, B. Davletov, A.G. Petrenko, and T.C. Sudhof
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Cold Spring Harb Symp Quant Biol, January 1, 1992; 57(0): 483 - 490.
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J. Biol. Chem.Home page
S. Wittemann, M. D. Mark, J. Rettig, and S. Herlitze
Synaptic Localization and Presynaptic Function of Calcium Channel beta 4-Subunits in Cultured Hippocampal Neurons
J. Biol. Chem., November 22, 2000; 275(48): 37807 - 37814.
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Proc. Natl. Acad. Sci. USAHome page
L. Tarsa and Y. Goda
Synaptophysin regulates activity-dependent synapse formation in cultured hippocampal neurons
PNAS, January 22, 2002; 99(2): 1012 - 1016.
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