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Synaptic laminin prevents glial entry into the synaptic cleft

Author

Listed:
  • Bruce L. Patton

    (Washington University School of Medicine)

  • Arlene Y. Chiu

    (Beckman Research Institute of the City of Hope)

  • Joshua R. Sanes

    (Washington University School of Medicine)

Abstract

Presynaptic and postsynaptic membranes directly oppose each other at chemical synapses, minimizing the delay in transmitting information across the synaptic cleft. Extrasynaptic neuronal surfaces, in contrast, are almost entirely covered by processes from glial cells1. The exclusion of glial cells from the synaptic cleft, and the long-term stability of synapses, presumably result in large part from the tight adhesion between presynaptic and postsynaptic elements2,3. Here we show that there is another requirement for synaptic maintenance: glial cells of the skeletal neuromuscular synapse, Schwann cells, are actively inhibited from entering the synaptic cleft between the motor nerve terminal and the muscle fibre. One inhibitory component is laminin 11, a heterotrimeric glycoprotein that is concentrated in the synaptic cleft4. Regulation of an inhibitory interaction between glial cells and synaptic cleft components may contribute to synaptic rearrangements, and loss of this inhibition may underlie the loss of synapses that results from injury to the postsynaptic cell5,6,7,8,9,10,11,12.

Suggested Citation

  • Bruce L. Patton & Arlene Y. Chiu & Joshua R. Sanes, 1998. "Synaptic laminin prevents glial entry into the synaptic cleft," Nature, Nature, vol. 393(6686), pages 698-701, June.
  • Handle: RePEc:nat:nature:v:393:y:1998:i:6686:d:10.1038_31502
    DOI: 10.1038/31502
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    1. Anna Konopka & Andre Zeug & Anna Skupien & Beata Kaza & Franziska Mueller & Agnieszka Chwedorowicz & Evgeni Ponimaskin & Grzegorz M Wilczynski & Joanna Dzwonek, 2016. "Cleavage of Hyaluronan and CD44 Adhesion Molecule Regulate Astrocyte Morphology via Rac1 Signalling," PLOS ONE, Public Library of Science, vol. 11(5), pages 1-14, May.

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