Literature DB >> 18431052

Developmental and regional patterns of GAP-43 immunoreactivity in a metamorphosing brain.

Andrea Megela Simmons1, Leslie H Tanyu, Seth S Horowitz, Judith A Chapman, Rebecca A Brown.   

Abstract

Growth-associated protein-43 is typically expressed at high levels in the nervous system during development. In adult animals, its expression is lower, but still observable in brain areas showing structural or functional plasticity. We examined patterns of GAP-43 immunoreactivity in the brain of the bullfrog, an animal whose nervous system undergoes considerable reorganization across metamorphic development and retains a strong capacity for plasticity in adulthood. Immunolabeling was mostly diffuse in hatchling tadpoles, but became progressively more discrete as larval development proceeded. In many brain areas, intensity of immunolabel peaked at metamorphic climax, the time of final transition from aquatic to semi-terrestrial life. Changes in intensity of GAP-43 expression in the medial vestibular nucleus, superior olivary nucleus, and torus semicircularis appeared correlated with stage-dependent functional changes in processing auditory stimuli. Immunolabeling in the Purkinje cell layer of the cerebellum and in the cerebellar nucleus was detectable at most developmental time points. Heavy immunolabel was present from early larval stages through the end of climax in the thalamus (ventromedial, anterior, posterior, central nuclei). Immunolabel in the tadpole telencephalon was observed around the lateral ventricles, and in the medial septum and ventral striatum. In postmetamorphic animals, immunoreactivity was confined mainly to the ventricular zones and immediately adjacent cell layers. GAP-43 expression was present in olfactory, auditory and optic cranial nerves throughout larval and postmetamorphic life. The continued expression of GAP-43 in brain nuclei and in cranial nerves throughout development and into adulthood reflects the high regenerative potential of the bullfrog's central nervous system. (c) 2008 S. Karger AG, Basel

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Year:  2008        PMID: 18431052      PMCID: PMC3257825          DOI: 10.1159/000127045

Source DB:  PubMed          Journal:  Brain Behav Evol        ISSN: 0006-8977            Impact factor:   1.808


  52 in total

1.  Axonal regeneration from CNS neurons in the cerebellum and brainstem of adult rats: correlation with the patterns of expression and distribution of messenger RNAs for L1, CHL1, c-jun and growth-associated protein-43.

Authors:  V Chaisuksunt; Y Zhang; P N Anderson; G Campbell; E Vaudano; M Schachner; A R Lieberman
Journal:  Neuroscience       Date:  2000       Impact factor: 3.590

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Authors:  A B Oestreicher; W H Gispen
Journal:  Brain Res       Date:  1986-06-11       Impact factor: 3.252

3.  A protein induced during nerve growth (GAP-43) is a major component of growth-cone membranes.

Authors:  J H Skene; R D Jacobson; G J Snipes; C B McGuire; J J Norden; J A Freeman
Journal:  Science       Date:  1986-08-15       Impact factor: 47.728

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Authors:  R D Jacobson; I Virág; J H Skene
Journal:  J Neurosci       Date:  1986-06       Impact factor: 6.167

Review 5.  Control of the development of the ipsilateral retinothalamic projection in Xenopus laevis by thyroxine: results and speculation.

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Journal:  J Neurobiol       Date:  1986-05

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Authors:  B Fritzsch; A M Nikundiwe; U Will
Journal:  J Comp Neurol       Date:  1984-11-01       Impact factor: 3.215

7.  Retinal ganglion cell terminals change their projection sites during larval development of Rana pipiens.

Authors:  T A Reh; M Constantine-Paton
Journal:  J Neurosci       Date:  1984-02       Impact factor: 6.167

8.  Cell proliferation in the forebrain and midbrain of the adult bullfrog, Rana catesbeiana.

Authors:  Andrea Megela Simmons; Seth S Horowitz; Rebecca A Brown
Journal:  Brain Behav Evol       Date:  2007-09-20       Impact factor: 1.808

9.  Growth-associated protein, GAP-43, a polypeptide that is induced when neurons extend axons, is a component of growth cones and corresponds to pp46, a major polypeptide of a subcellular fraction enriched in growth cones.

Authors:  K F Meiri; K H Pfenninger; M B Willard
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

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Authors:  W Wilczynski; R G Northcutt
Journal:  J Comp Neurol       Date:  1983-03-01       Impact factor: 3.215

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  1 in total

Review 1.  Comparative aspects of adult neural stem cell activity in vertebrates.

Authors:  Heiner Grandel; Michael Brand
Journal:  Dev Genes Evol       Date:  2012-11-22       Impact factor: 0.900

  1 in total

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