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Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle

PURPOSE: To spatially and temporally define ocular motor nerve development in the presence and absence of extraocular muscles (EOMs). METHODS: Myf5(cre) mice, which in the homozygous state lack EOMs, were crossed to an Isl(MN):GFP reporter line to fluorescently label motor neuron cell bodies and axo...

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Autores principales: Michalak, Suzanne M., Whitman, Mary C., Park, Jong G., Tischfield, Max A., Nguyen, Elaine H., Engle, Elizabeth C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403115/
https://www.ncbi.nlm.nih.gov/pubmed/28437527
http://dx.doi.org/10.1167/iovs.16-21268
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author Michalak, Suzanne M.
Whitman, Mary C.
Park, Jong G.
Tischfield, Max A.
Nguyen, Elaine H.
Engle, Elizabeth C.
author_facet Michalak, Suzanne M.
Whitman, Mary C.
Park, Jong G.
Tischfield, Max A.
Nguyen, Elaine H.
Engle, Elizabeth C.
author_sort Michalak, Suzanne M.
collection PubMed
description PURPOSE: To spatially and temporally define ocular motor nerve development in the presence and absence of extraocular muscles (EOMs). METHODS: Myf5(cre) mice, which in the homozygous state lack EOMs, were crossed to an Isl(MN):GFP reporter line to fluorescently label motor neuron cell bodies and axons. Embryonic day (E) 11.5 to E15.5 wild-type and Myf5(cre/cre):Isl(MN):GFP whole mount embryos and dissected orbits were imaged by confocal microscopy to visualize the developing oculomotor, trochlear, and abducens nerves in the presence and absence of EOMs. E11.5 and E18.5 brainstems were serially sectioned and stained for Islet1 to determine the fate of ocular motor neurons. RESULTS: At E11.5, all three ocular motor nerves in mutant embryos approached the orbit with a trajectory similar to that of wild-type. Subsequently, while wild-type nerves send terminal branches that contact target EOMs in a stereotypical pattern, the Myf5(cre/cre) ocular motor nerves failed to form terminal branches, regressed, and by E18.5 two-thirds of their corresponding motor neurons died. Comparisons between mutant and wild-type embryos revealed novel aspects of trochlear and oculomotor nerve development. CONCLUSIONS: We delineated mouse ocular motor nerve spatial and temporal development in unprecedented detail. Moreover, we found that EOMs are not necessary for initial outgrowth and guidance of ocular motor axons from the brainstem to the orbit but are required for their terminal branching and survival. These data suggest that intermediate targets in the mesenchyme provide cues necessary for appropriate targeting of ocular motor axons to the orbit, while EOM cues are responsible for terminal branching and motor neuron survival.
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spelling pubmed-54031152017-04-30 Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle Michalak, Suzanne M. Whitman, Mary C. Park, Jong G. Tischfield, Max A. Nguyen, Elaine H. Engle, Elizabeth C. Invest Ophthalmol Vis Sci Eye Movements, Strabismus, Amblyopia and Neuro-Ophthalmology PURPOSE: To spatially and temporally define ocular motor nerve development in the presence and absence of extraocular muscles (EOMs). METHODS: Myf5(cre) mice, which in the homozygous state lack EOMs, were crossed to an Isl(MN):GFP reporter line to fluorescently label motor neuron cell bodies and axons. Embryonic day (E) 11.5 to E15.5 wild-type and Myf5(cre/cre):Isl(MN):GFP whole mount embryos and dissected orbits were imaged by confocal microscopy to visualize the developing oculomotor, trochlear, and abducens nerves in the presence and absence of EOMs. E11.5 and E18.5 brainstems were serially sectioned and stained for Islet1 to determine the fate of ocular motor neurons. RESULTS: At E11.5, all three ocular motor nerves in mutant embryos approached the orbit with a trajectory similar to that of wild-type. Subsequently, while wild-type nerves send terminal branches that contact target EOMs in a stereotypical pattern, the Myf5(cre/cre) ocular motor nerves failed to form terminal branches, regressed, and by E18.5 two-thirds of their corresponding motor neurons died. Comparisons between mutant and wild-type embryos revealed novel aspects of trochlear and oculomotor nerve development. CONCLUSIONS: We delineated mouse ocular motor nerve spatial and temporal development in unprecedented detail. Moreover, we found that EOMs are not necessary for initial outgrowth and guidance of ocular motor axons from the brainstem to the orbit but are required for their terminal branching and survival. These data suggest that intermediate targets in the mesenchyme provide cues necessary for appropriate targeting of ocular motor axons to the orbit, while EOM cues are responsible for terminal branching and motor neuron survival. The Association for Research in Vision and Ophthalmology 2017-04 /pmc/articles/PMC5403115/ /pubmed/28437527 http://dx.doi.org/10.1167/iovs.16-21268 Text en Copyright 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Eye Movements, Strabismus, Amblyopia and Neuro-Ophthalmology
Michalak, Suzanne M.
Whitman, Mary C.
Park, Jong G.
Tischfield, Max A.
Nguyen, Elaine H.
Engle, Elizabeth C.
Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title_full Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title_fullStr Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title_full_unstemmed Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title_short Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
title_sort ocular motor nerve development in the presence and absence of extraocular muscle
topic Eye Movements, Strabismus, Amblyopia and Neuro-Ophthalmology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403115/
https://www.ncbi.nlm.nih.gov/pubmed/28437527
http://dx.doi.org/10.1167/iovs.16-21268
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