Literature DB >> 9712655

Trigeminal ganglion axons are repelled by their presumptive targets.

M W Rochlin1, A I Farbman.   

Abstract

Previous work suggested that in mouse, presumptive targets of the trigeminal ganglion, rather than intermediate structures, attract pioneer axons from the time their growth cones exit the ganglion (Lumsden and Davies, 1986). In rat we find that some presumptive targets repel trigeminal axons. The repellant activity is concentrated in the anterior and ventral epithelium of the mandibular arch at embryonic day 12 (E12) and was also present in the maxillary arch. The activity is blocked by anti-neuropilin-1. E13 mandible explants repel trigeminal axons during the first day of outgrowth in vitro, but thereafter permit or attract trigeminal ganglion axon outgrowth. By E14, lingual nerve afferents first enter the tongue in vivo, and the repellant influence becomes restricted to the midline. The progressive restriction of the repellant influence may contribute to the in vivo progression of nerve development: the earliest afferents turn anteriorly lateral to the tongue, but subsequently arriving afferents advance into the tongue and then turn away from the midline. Thus, the repellant may influence the order of nerve branch development and the timing of innervation of epithelial and subepithelial targets. Heterochronic studies revealed that the loss of repellant influence from presumptive lateral tongue surface results from downregulation of the repellant activity, not of responsiveness to the repellant. Because presumptive targets repel trigeminal axons during the initial stages of advance from the trigeminal ganglion and do not have a net attractive influence until after afferents have arrived near the target, intermediate structures must guide these axons initially.

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Year:  1998        PMID: 9712655      PMCID: PMC6792978     

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


  49 in total

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Authors:  D Y Stainier; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

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Journal:  Neuron       Date:  1996-07       Impact factor: 17.173

3.  Deleted in Colorectal Cancer (DCC) encodes a netrin receptor.

Authors:  K Keino-Masu; M Masu; L Hinck; E D Leonardo; S S Chan; J G Culotti; M Tessier-Lavigne
Journal:  Cell       Date:  1996-10-18       Impact factor: 41.582

4.  Localized collapsing cues can steer growth cones without inducing their full collapse.

Authors:  J Fan; J A Raper
Journal:  Neuron       Date:  1995-02       Impact factor: 17.173

5.  Neuropilin is a receptor for the axonal chemorepellent Semaphorin III.

Authors:  Z He; M Tessier-Lavigne
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

6.  Neuropilin is a semaphorin III receptor.

Authors:  A L Kolodkin; D V Levengood; E G Rowe; Y T Tai; R J Giger; D D Ginty
Journal:  Cell       Date:  1997-08-22       Impact factor: 41.582

7.  NGF and neurotrophin-3 both activate TrkA on sympathetic neurons but differentially regulate survival and neuritogenesis.

Authors:  D J Belliveau; I Krivko; J Kohn; C Lachance; C Pozniak; D Rusakov; D Kaplan; F D Miller
Journal:  J Cell Biol       Date:  1997-01-27       Impact factor: 10.539

8.  The sensory innervation of the mouse spinal cord may be patterned by differential expression of and differential responsiveness to semaphorins.

Authors:  A W Püschel; R H Adams; H Betz
Journal:  Mol Cell Neurosci       Date:  1996-05       Impact factor: 4.314

9.  Collapsin: a protein in brain that induces the collapse and paralysis of neuronal growth cones.

Authors:  Y Luo; D Raible; J A Raper
Journal:  Cell       Date:  1993-10-22       Impact factor: 41.582

10.  Distribution of laminin and fibronectin along peripheral trigeminal axon pathways in the developing chick.

Authors:  M J Riggott; S A Moody
Journal:  J Comp Neurol       Date:  1987-04-22       Impact factor: 3.215

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3.  Role of brain-derived neurotrophic factor in target invasion in the gustatory system.

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4.  Chemoattraction and chemorepulsion of olfactory bulb axons by different secreted semaphorins.

Authors:  F de Castro; L Hu; H Drabkin; C Sotelo; A Chédotal
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5.  Neurotrophin-4 regulates the survival of gustatory neurons earlier in development using a different mechanism than brain-derived neurotrophic factor.

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6.  Brain-derived neurotrophic factor attracts geniculate ganglion neurites during embryonic targeting.

Authors:  Natalia Hoshino; Phillip Vatterott; Amina Egwiekhor; M William Rochlin
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7.  Epithelial-derived brain-derived neurotrophic factor is required for gustatory neuron targeting during a critical developmental period.

Authors:  Liqun Ma; Grace F Lopez; Robin F Krimm
Journal:  J Neurosci       Date:  2009-03-18       Impact factor: 6.167

8.  Distinct roles for neuropilin1 and neuropilin2 during mouse corneal innervation.

Authors:  Chelsey C McKenna; Ravi P Munjaal; Peter Y Lwigale
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Review 9.  Factors that regulate embryonic gustatory development.

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Journal:  BMC Neurosci       Date:  2007-09-18       Impact factor: 3.288

10.  The neurotrophin receptor p75 regulates gustatory axon branching and promotes innervation of the tongue during development.

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