Literature DB >> 8987787

A transcription-dependent switch controls competence of adult neurons for distinct modes of axon growth.

D S Smith1, J H Skene.   

Abstract

Although maturing neurons undergo a precipitous decline in the expression of genes associated with developmental axon growth, structural changes in axon arbors occur in the adult nervous system under both normal and pathological conditions. Furthermore, some neurons support extensive regrowth of long axons after nerve injury. Analysis of adult dorsal root ganglion (DRG) neurons in culture now shows that competence for distinct types of axon growth depends on different patterns of gene expression. In the absence of ongoing transcription, newly isolated neurons can extend compact, highly branched arbors during the first day in culture. Neurons subjected to peripheral axon injury 2-7 d before plating support a distinct mode of growth characterized by rapid extension of long, sparsely branched axons. A transition from "arborizing" to "elongating" growth occurs in naive adult neurons after approximately 24 hr in culture but requires a discrete period of new transcription after removal of the ganglia from the intact animal. Thus, peripheral axotomy-by nerve crush or during removal of DRGs--induces a transcription-dependent change that alters the type of axon growth that can be executed by these adult neurons. This transition appears to be triggered, in large part, by interruption of retrogradely transported signals, because blocking axonal transport in vivo can elicit competence for elongating growth in many DRG neurons. In contrast to peripheral axotomy, interruption of the centrally projecting axons of DRG neurons in vivo leads to subsequent growth in vitro that is intermediate between "arborizing" and "elongating" growth. This suggests that the transition between these two modes of growth is a multistep process and that individual steps may be regulated separately. These observations together suggest that structural remodeling in the adult nervous system need not involve the same molecular apparatus as long axon growth during development and regeneration.

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Year:  1997        PMID: 8987787      PMCID: PMC6573254     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  77 in total

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Authors:  D J Schreyer; J H Skene
Journal:  J Neurosci       Date:  1991-12       Impact factor: 6.167

2.  GAP-43 in the axons of mammalian CNS neurons regenerating into peripheral nerve grafts.

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Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  G0 is a major growth cone protein subject to regulation by GAP-43.

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Journal:  Nature       Date:  1990-04-26       Impact factor: 49.962

4.  GAP-43 gene expression during development: persistence in a distinctive set of neurons in the mature central nervous system.

Authors:  S M De la Monte; H J Federoff; S C Ng; E Grabczyk; M C Fishman
Journal:  Brain Res Dev Brain Res       Date:  1989-04-01

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Authors:  N R Smalheiser
Journal:  Brain Res Dev Brain Res       Date:  1989-01-01

6.  Distribution of GAP-43 mRNA in the brain stem of adult rats as evidenced by in situ hybridization: localization within monoaminergic neurons.

Authors:  C Bendotti; A Servadio; R Samanin
Journal:  J Neurosci       Date:  1991-03       Impact factor: 6.167

Review 7.  Plasticity of developing and adult dorsal root ganglion neurons as revealed in vitro.

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8.  Mossy fiber synaptic reorganization induced by kindling: time course of development, progression, and permanence.

Authors:  J E Cavazos; G Golarai; T P Sutula
Journal:  J Neurosci       Date:  1991-09       Impact factor: 6.167

9.  Developmentally regulated expression of pleiotrophin, a novel heparin binding growth factor, in the nervous system of the rat.

Authors:  A Wanaka; S L Carroll; J Milbrandt
Journal:  Brain Res Dev Brain Res       Date:  1993-03-19

10.  Axonally transported proteins associated with axon growth in rabbit central and peripheral nervous systems.

Authors:  J H Skene; M Willard
Journal:  J Cell Biol       Date:  1981-04       Impact factor: 10.539

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  185 in total

1.  A functional role for intra-axonal protein synthesis during axonal regeneration from adult sensory neurons.

Authors:  J Q Zheng; T K Kelly; B Chang; S Ryazantsev; A K Rajasekaran; K C Martin; J L Twiss
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

2.  Axonal rejoining inhibits injury-induced long-term changes in Aplysia sensory neurons in vitro.

Authors:  S S Bedi; D L Glanzman
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

3.  Spinal cord injury triggers an intrinsic growth-promoting state in nociceptors.

Authors:  Supinder S Bedi; Michael T Lago; Luke I Masha; Robyn J Crook; Raymond J Grill; Edgar T Walters
Journal:  J Neurotrauma       Date:  2011-11-04       Impact factor: 5.269

4.  Axonal transcription factors signal retrogradely in lesioned peripheral nerve.

Authors:  Keren Ben-Yaakov; Shachar Y Dagan; Yael Segal-Ruder; Ophir Shalem; Deepika Vuppalanchi; Dianna E Willis; Dmitry Yudin; Ida Rishal; Franziska Rother; Michael Bader; Armin Blesch; Yitzhak Pilpel; Jeffery L Twiss; Mike Fainzilber
Journal:  EMBO J       Date:  2012-01-13       Impact factor: 11.598

5.  Limited availability of ZBP1 restricts axonal mRNA localization and nerve regeneration capacity.

Authors:  Christopher J Donnelly; Dianna E Willis; Mei Xu; Chhavy Tep; Chunsu Jiang; Soonmoon Yoo; N Carolyn Schanen; Catherine B Kirn-Safran; Jan van Minnen; Arthur English; Sung Ok Yoon; Gary J Bassell; Jeffery L Twiss
Journal:  EMBO J       Date:  2011-09-30       Impact factor: 11.598

6.  Roles of membrane trafficking in nerve repair and regeneration.

Authors:  Elizabeth Tuck; Valeria Cavalli
Journal:  Commun Integr Biol       Date:  2010-05

7.  Dual leucine zipper kinase is required for retrograde injury signaling and axonal regeneration.

Authors:  Jung Eun Shin; Yongcheol Cho; Bogdan Beirowski; Jeffrey Milbrandt; Valeria Cavalli; Aaron DiAntonio
Journal:  Neuron       Date:  2012-06-21       Impact factor: 17.173

Review 8.  Molecular and Cellular Mechanisms of Axonal Regeneration After Spinal Cord Injury.

Authors:  Erna A van Niekerk; Mark H Tuszynski; Paul Lu; Jennifer N Dulin
Journal:  Mol Cell Proteomics       Date:  2015-12-22       Impact factor: 5.911

9.  Axonal transport of neural membrane protein 35 mRNA increases axon growth.

Authors:  Tanuja T Merianda; Deepika Vuppalanchi; Soonmoon Yoo; Armin Blesch; Jeffery L Twiss
Journal:  J Cell Sci       Date:  2012-10-24       Impact factor: 5.285

10.  HSP90 is a chaperone for DLK and is required for axon injury signaling.

Authors:  Scott Karney-Grobe; Alexandra Russo; Erin Frey; Jeffrey Milbrandt; Aaron DiAntonio
Journal:  Proc Natl Acad Sci U S A       Date:  2018-10-01       Impact factor: 11.205

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