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Pleiotropic molecules in axon regeneration and neuroinflammation

Journal

EXPERIMENTAL NEUROLOGY
Volume 258, Issue -, Pages 17-23

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2014.04.031

Keywords

Neuroinflammation; Axon regeneration; Myelin-associated inhibitors and receptors; Proteoglycans

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Funding

  1. Department of Neuroscience, The Ohio State University
  2. Research Grants Council of the Hong Kong Special Administrative Region Government, Centre for Biosystems, Neuroscience, and Nanotechnology at City University of Hong Kong [CityU 161212, CityU 160813]
  3. Seed Funding [7003028]

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Neuroinflammation is the foremost defense reaction of the nervous system to most if not all insults. Injuries to the central and peripheral nervous system (CNS and PNS) are followed by immediate activation of innate immune cells and infiltration of peripheral immune cells, amid waves of upregulation of numerous inflammatory mediators. Prolonged inflammation can lead to secondary tissue damage and prohibit regeneration of the injured nervous system. The regulation of inflammation and neuroregeneration are orchestrated through a complex network of signal transduction. Interestingly, many molecules play pleiotropic roles in both processes. Growing evidence implicates a handful of axon regeneration regulators in the processes of neuroinflammation, among which are the myelin and glial scar associated axon growth inhibitors and their axonal receptors. In this article, we will review the roles of these canonical axon regeneration regulators in neuroinflammation. Published by Elsevier Inc.

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