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from
Section B2
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Determinants of regeneration in the injured nervous system
By
Joel M. Levine, Department of Neurobiology and Behavior, State University of New York at Stony Brook, Stony Brook, NY, USA,
Lorne M. Mendell, Department of Neurobiology and Behavior, State University of New York at Stony Brook, Stony Brook, NY, USA
Edited by
Michael Selzer, University of Pennsylvania,Stephanie Clarke, Université de Lausanne, Switzerland,Leonardo Cohen, National Institute of Mental Health, Bethesda, Maryland,Pamela Duncan, University of Florida,Fred Gage, Salk Institute for Biological Studies, San Diego
This chapter reviews the biology of neurotrophins (NTs) and their receptors with an emphasis on their use to encourage nerve regeneration after damage to both the central and peripheral nervous system. NTs bind to a receptor complex comprised of two components: p75 and a tropomyosin-related kinase (Trk) transmembrane receptor protein tyrosine Kinase. Ligand binding induces Trk subunit dimerization and the autophosphorylation of multiple tyrosine residues. This autophosphorylation initiates several different intracellular signaling cascades that are described in the chapter. p75 can also play an important role as a negative regulator of axon growth by virtue of its interactions with the rho GTPase. Damaged peripheral axons undergo a characteristic sequence of morphological and physiological changes. The specificity of different NTs in promoting regeneration of different functional classes of dorsal root (DR) fibers suggests that spinal axons should also be selectively responsive to different NTs.
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