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Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm

PURPOSE: Regeneration of optic nerve axons after injury can be facilitated by several approaches, but misguidance at the optic chiasm is often observed. We characterized guidance cues in the embryonic visual system and adult optic chiasm before and after optic nerve crush (ONC) injury to better unde...

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Autores principales: Conceição, Raquel, Evans, Rachel S., Pearson, Craig S., Hänzi, Barbara, Osborne, Andrew, Deshpande, Sarita S., Martin, Keith R., Barber, Amanda C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859889/
https://www.ncbi.nlm.nih.gov/pubmed/31731293
http://dx.doi.org/10.1167/iovs.19-26732
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author Conceição, Raquel
Evans, Rachel S.
Pearson, Craig S.
Hänzi, Barbara
Osborne, Andrew
Deshpande, Sarita S.
Martin, Keith R.
Barber, Amanda C.
author_facet Conceição, Raquel
Evans, Rachel S.
Pearson, Craig S.
Hänzi, Barbara
Osborne, Andrew
Deshpande, Sarita S.
Martin, Keith R.
Barber, Amanda C.
author_sort Conceição, Raquel
collection PubMed
description PURPOSE: Regeneration of optic nerve axons after injury can be facilitated by several approaches, but misguidance at the optic chiasm is often observed. We characterized guidance cues in the embryonic visual system and adult optic chiasm before and after optic nerve crush (ONC) injury to better understand barriers to optic nerve regeneration in adults. METHODS: Radial glial (RC2/BLBP/Slit1), developmental (Pax2) and extracellular markers (CSPG: H2B/CS-56) were assessed in C57BL/6J mice by immunohistochemistry. RC2, BLBP, Slit1, and CSPG are known inhibitory guidance cues while Pax2 is a permissive guidance cue. RESULTS: At embryonic day 15.5 (E.15.5), RC2 and BLBP were identified superior to, and extending through, the optic chiasm. The optic chiasm was BLBP(−ve) in adult uninjured mice but BLBP(+ve) in adult mice 10 days after ONC injury. The reverse was true for RC2. Both BLBP and RC2 were absent in adult mice 6 weeks post-ONC. Slit1 was present in the optic chiasm midline and optic tracts in embryonic samples but was absent in uninjured adult tissue. Slit1 was observed superior to and at the midline of the optic chiasm 10 days post-ONC but absent 6 weeks after injury. Pax2 was expressed at the junction between the optic nerve and optic chiasm in embryonic brain tissue. In embryonic sections, CS-56 was observed at the junction between the optic chiasm and optic tract, and immediately superior to the optic chiasm. Both 2H6 and CS-56 staining was absent in uninjured and ONC-injured adult brains. CONCLUSION: Differences in guidance cue expression during development, in adulthood and after injury may contribute to misguidance of regenerating RGC axons in the adult optic chiasm.
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spelling pubmed-68598892019-11-27 Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm Conceição, Raquel Evans, Rachel S. Pearson, Craig S. Hänzi, Barbara Osborne, Andrew Deshpande, Sarita S. Martin, Keith R. Barber, Amanda C. Invest Ophthalmol Vis Sci Anatomy and Pathology/Oncology PURPOSE: Regeneration of optic nerve axons after injury can be facilitated by several approaches, but misguidance at the optic chiasm is often observed. We characterized guidance cues in the embryonic visual system and adult optic chiasm before and after optic nerve crush (ONC) injury to better understand barriers to optic nerve regeneration in adults. METHODS: Radial glial (RC2/BLBP/Slit1), developmental (Pax2) and extracellular markers (CSPG: H2B/CS-56) were assessed in C57BL/6J mice by immunohistochemistry. RC2, BLBP, Slit1, and CSPG are known inhibitory guidance cues while Pax2 is a permissive guidance cue. RESULTS: At embryonic day 15.5 (E.15.5), RC2 and BLBP were identified superior to, and extending through, the optic chiasm. The optic chiasm was BLBP(−ve) in adult uninjured mice but BLBP(+ve) in adult mice 10 days after ONC injury. The reverse was true for RC2. Both BLBP and RC2 were absent in adult mice 6 weeks post-ONC. Slit1 was present in the optic chiasm midline and optic tracts in embryonic samples but was absent in uninjured adult tissue. Slit1 was observed superior to and at the midline of the optic chiasm 10 days post-ONC but absent 6 weeks after injury. Pax2 was expressed at the junction between the optic nerve and optic chiasm in embryonic brain tissue. In embryonic sections, CS-56 was observed at the junction between the optic chiasm and optic tract, and immediately superior to the optic chiasm. Both 2H6 and CS-56 staining was absent in uninjured and ONC-injured adult brains. CONCLUSION: Differences in guidance cue expression during development, in adulthood and after injury may contribute to misguidance of regenerating RGC axons in the adult optic chiasm. The Association for Research in Vision and Ophthalmology 2019-11 /pmc/articles/PMC6859889/ /pubmed/31731293 http://dx.doi.org/10.1167/iovs.19-26732 Text en Copyright 2019 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 Anatomy and Pathology/Oncology
Conceição, Raquel
Evans, Rachel S.
Pearson, Craig S.
Hänzi, Barbara
Osborne, Andrew
Deshpande, Sarita S.
Martin, Keith R.
Barber, Amanda C.
Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title_full Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title_fullStr Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title_full_unstemmed Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title_short Expression of Developmentally Important Axon Guidance Cues in the Adult Optic Chiasm
title_sort expression of developmentally important axon guidance cues in the adult optic chiasm
topic Anatomy and Pathology/Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859889/
https://www.ncbi.nlm.nih.gov/pubmed/31731293
http://dx.doi.org/10.1167/iovs.19-26732
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