4.7 Article

Intrinsic facilitation of adult peripheral nerve regeneration by the Sonic hedgehog morphogen

期刊

EXPERIMENTAL NEUROLOGY
卷 271, 期 -, 页码 493-505

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2015.07.018

关键词

Peripheral nerve; Regeneration; Sonic hedgehog protein; Nerve injury

资金

  1. Canadian Institutes of Health Research (CIHR) [FRN15686]
  2. University of Alberta Hospital Foundation
  3. Department of Medicine
  4. Division of Neurology, Faculty of Medicine and Dentistry, University of Alberta
  5. Alberta Heritage Foundation for Medical Research
  6. Denyse-Lake-LaJoie fellowship of the University of Calgary

向作者/读者索取更多资源

Intrinsic molecular determinants of neurodevelopmental outcomes assume new, albeit related roles during adult neural regeneration. Here we studied and identified a facilitatory role for Sonic hedgehog protein (Shh), a morphogen that influences motor neuron floor plate architecture, during adult peripheral neuron regeneration. Shh and its receptors were expressed in adult dorsal root ganglia (DRG) neurons, axons and glia and trended toward higher levels following axotomy injury. Knockdown of Shh in adult sensory neurons resulted in decreased outgrowth and branching in vitro, identifying a role for Shh in facilitating outgrowth. The findings argued for an intrinsic action to support neuron regeneration. Support of advancement and turning however, were not identified in adult sensory neuron growth cones in response to local extrinsic gradients of Shh. That intrinsic Shh supported the regrowth of peripheral nerves after injury was confirmed by the analysis of axon regrowth from the proximal stumps of transected sciatic nerves. By exposing regenerating axons to local infusions of Shh siRNA in vivo within a conduit bridging the transected proximal and distal stumps, we achieved local knockdown of Shh. In response, there was attenuated axonal and Schwann cell outgrowth beyond the transection zone. Unlike its role during neurodevelopment, Shh facilitates but does not confer regenerative outgrowth properties to adult neurons alone. Exploring the differing properties of morphogens and related proteins in the adult nervous system identifies new and important roles for them. (C) 2015 Published by Elsevier Inc.

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