Medical Journals

Formation of Presynaptic Terminals at Predefined Sites Along Axons.

Authors:
  • Sabo Shasta L
  • Gomes Raquel A
  • McAllister A Kimberley

From: Center for Neuroscience, University of California, Davis, Davis, California 95616, USA.

The Journal of neuroscience : the official journal of the Society for Neuroscience

  • Publish Date: Oct 2006
  • ISSN: 1529-2401
  • Volume: 26
  • Issue: 42
  • Pages: 10813-25
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Sabo Shasta L, Gomes Raquel A, McAllister A Kimberley, et al. Formation of Presynaptic Terminals at Predefined Sites Along Axons.. J. Neurosci. Oct 2006;26:10813-25

Abstract

What determines where synapses will form along an axon or how proteins are deposited at nascent synapses remains unknown. Here, we show that the initial formation of presynaptic terminals occurs preferentially at predefined sites within the axons of cortical neurons. Time-lapse imaging of synaptic vesicle protein transport vesicles (STVs) indicates that STVs pause repeatedly at these sites, even in the absence of neuronal or glial contact. Contact with a neuroligin-expressing non-neuronal cell induces formation of presynaptic terminals specifically at these STV pause sites. Remarkably, formation of stable contacts with dendritic filopodia also occurs selectively at STV pause sites. Although it is not yet known which molecules comprise the predefined sites, STV pausing is regulated by cues that affect synaptogenesis. Overall, these data are consistent with the hypothesis that regulation of STV pausing might be an important mechanism for accumulation of presynaptic proteins at nascent synapses and support a new model in which many en passant synapses form specifically at predefined sites in young axons.

Mesh Headings (Keywords): Animals, Axons, Cell Line, Cells, Cultured, Green Fluorescent Proteins, Humans, Mice, Mice, Knockout, Presynaptic Terminals, Protein Transport, Rats, Synaptic Vesicles, Vesicle-Associated Membrane Protein 2


Check for Full Text / PubMed Unique Identifier (PMID): 17050720


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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