Genetic Analysis of the Organization, Development, and Plasticity of Corneal Innervation in Mice.


Journal

The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN: 1529-2401
Titre abrégé: J Neurosci
Pays: United States
ID NLM: 8102140

Informations de publication

Date de publication:
13 02 2019
Historique:
received: 02 06 2018
revised: 05 10 2018
accepted: 24 11 2018
pubmed: 28 12 2018
medline: 18 12 2019
entrez: 28 12 2018
Statut: ppublish

Résumé

The cornea has the densest sensory innervation of the body, originating primarily from neurons in the trigeminal ganglion. The basic principles of cornea nerve patterning have been established many years ago using classic neuroanatomical methods, such as immunocytochemistry and electrophysiology. Our understanding of the morphology and distribution of the sensory nerves in the skin has considerably progressed over the past few years through the generation and analysis of a variety of genetically modified mouse lines. Surprisingly, these lines were not used to study corneal axons. Here, we have screened a collection of transgenic and knockin mice (of both sexes) to select lines allowing the visualization and genetic manipulation of corneal nerves. We identified multiple lines, including some in which different types of corneal axons can be simultaneously observed with fluorescent proteins expressed in a combinatorial manner. We also provide the first description of the morphology and arborization of single corneal axons and identify three main types of branching pattern. We applied this genetic strategy to the analysis of corneal nerve development and plasticity. We provide direct evidence for a progressive reduction of the density of corneal innervation during aging. We also show that the semaphorin receptor neuropilin-1 acts cell-autonomously to control the development of corneal axons and that early axon guidance defects have long-term consequences on corneal innervation.

Identifiants

pubmed: 30587537
pii: JNEUROSCI.1401-18.2018
doi: 10.1523/JNEUROSCI.1401-18.2018
pmc: PMC6381234
doi:

Substances chimiques

Tamoxifen 094ZI81Y45
Neuropilin-1 144713-63-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1150-1168

Informations de copyright

Copyright © 2019 the authors 0270-6474/19/391150-19$15.00/0.

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Auteurs

Nacim Bouheraoua (N)

Institut de la Vision, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, F-75012 Paris, France, alain.chedotal@inserm.fr nacim.bouheraoua@gmail.com.
Quinze-Vingts National Ophthalmology Hospital, Sorbonne Université, DHU Sight Restore, Institut National de la Santé et de la Recherche Médicale-DGOS CIC 1423, F-75012 Paris, France, and.

Stéphane Fouquet (S)

Institut de la Vision, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, F-75012 Paris, France.

Maria Teresa Marcos-Almaraz (MT)

Institut de la Vision, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, F-75012 Paris, France.

Domna Karagogeos (D)

Department of Basic Science, Faculty of Medicine, University of Crete, Vassilika Vouton, Crete 71110, Greece.

Laurent Laroche (L)

Institut de la Vision, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, F-75012 Paris, France.
Quinze-Vingts National Ophthalmology Hospital, Sorbonne Université, DHU Sight Restore, Institut National de la Santé et de la Recherche Médicale-DGOS CIC 1423, F-75012 Paris, France, and.

Alain Chédotal (A)

Institut de la Vision, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, F-75012 Paris, France, alain.chedotal@inserm.fr nacim.bouheraoua@gmail.com.

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Classifications MeSH