Literature DB >> 7556549

Target influences on the morphology of trigeminal axons.

R S Erzurumlu1, S Jhaveri.   

Abstract

Axons grow in two stages: First, they exhibit rapid, target-directed extension; then they begin to collateralize and elaborate terminal arbors in their targets. To investigate possible regulatory influences on these phases of axon growth, we have used an in vitro paradigm in which we cocultured embryonic or postnatal rat trigeminal ganglion explants with isochronic, heterochronic, and/or heterotypic targets. Cultures were fixed after 5 days and ganglion cell processes were labeled with DiI. Trigeminal processes were able to regenerate into several peripheral targets as well as into CNS explants from trigeminal or nontrigeminal regions of the brain. In peripheral tissues, the processes showed target-specific growth patterns. In CNS tissue, the type of growth (unbranched extension versus collateralization/arbor formation) varied markedly with the explant age: If trigeminal ganglia were harvested at a time (E15) when their axons would be elongating in the embryo and cocultured with isochronic tissues, their processes had a simple morphology, were loosely bundled, and reconstituted a distinct fiber tract, mimicking their in vivo growth pattern. If, challenged by more mature tissue, axons of E15 ganglion cells formed discrete arbors. Finally, if trigeminal ganglia were harvested at an age (E20, PND 5) when their axons had already formed arbors in the brain and induced to innervate younger (E15) targets, their axons reverted back to the elongation stage. These results demonstrate that the target environment sets specific, developmentally regulated constraints on the patterns of growth manifested by primary sensory axons.

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Year:  1995        PMID: 7556549     DOI: 10.1006/exnr.1995.1061

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  9 in total

1.  Directional specificity and patterning of sensory axons in trigeminal ganglion-whisker pad cocultures.

Authors:  Emine Gunhan-Agar; Adam Haeberle; Reha S Erzurumlu
Journal:  Brain Res Dev Brain Res       Date:  2000-02-07

2.  p75 is important for axon growth and schwann cell migration during development.

Authors:  C A Bentley; K F Lee
Journal:  J Neurosci       Date:  2000-10-15       Impact factor: 6.167

3.  Local neurotrophin effects on central trigeminal axon growth patterns.

Authors:  P Hande Ozdinler; Emel Ulupinar; Reha S Erzurumlu
Journal:  Brain Res Dev Brain Res       Date:  2004-07-19

4.  Formation of cortical fields on a reduced cortical sheet.

Authors:  K J Huffman; Z Molnár; A Van Dellen; D M Kahn; C Blakemore; L Krubitzer
Journal:  J Neurosci       Date:  1999-11-15       Impact factor: 6.167

Review 5.  Molecular determinants of the face map development in the trigeminal brainstem.

Authors:  Reha S Erzurumlu; Zhou-Feng Chen; Mark F Jacquin
Journal:  Anat Rec A Discov Mol Cell Evol Biol       Date:  2006-02

6.  Target specific differentiation of peripheral trigeminal axons in rat-chick chimeric explant cocultures.

Authors:  A S Haeberle; R S Erzurumlu
Journal:  Brain Res Dev Brain Res       Date:  2001-11-26

7.  Differential effects of NGF and NT-3 on embryonic trigeminal axon growth patterns.

Authors:  E Ulupinar; M F Jacquin; R S Erzurumlu
Journal:  J Comp Neurol       Date:  2000-09-18       Impact factor: 3.215

8.  Slit2, a branching-arborization factor for sensory axons in the Mammalian CNS.

Authors:  P Hande Ozdinler; Reha S Erzurumlu
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

9.  Distinct modes of neuritic growth in purkinje neurons at different developmental stages: axonal morphogenesis and cellular regulatory mechanisms.

Authors:  Annarita de Luca; Stefania Vassallo; Beatriz Benitez-Temino; Gianluca Menichetti; Ferdinando Rossi; Annalisa Buffo
Journal:  PLoS One       Date:  2009-08-31       Impact factor: 3.240

  9 in total

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