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Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology

Various techniques have been explored to determine the uses and limitations of techniques that enable the adult CNS to regenerate, but relatively little attention has been given to the consideration of a "reconstructed" visual system. Using this approach, one can design experiments to stud...

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Autores principales: Zanakis, Michael F., Lowe, Howard F., Jacobsen, Glenn, LaCorte, Michael, Lee, Simone P., Hallas, Brian H.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565006/
https://www.ncbi.nlm.nih.gov/pubmed/2485119
http://dx.doi.org/10.1155/NP.1989.77
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author Zanakis, Michael F.
Lowe, Howard F.
Jacobsen, Glenn
LaCorte, Michael
Lee, Simone P.
Hallas, Brian H.
author_facet Zanakis, Michael F.
Lowe, Howard F.
Jacobsen, Glenn
LaCorte, Michael
Lee, Simone P.
Hallas, Brian H.
author_sort Zanakis, Michael F.
collection PubMed
description Various techniques have been explored to determine the uses and limitations of techniques that enable the adult CNS to regenerate, but relatively little attention has been given to the consideration of a "reconstructed" visual system. Using this approach, one can design experiments to study the uses of exogenous tissues in reestablishing neuronal circuits that have been damaged. Toward this end, experiments were designed to determine whether embryonic retinal ganglion cells can project axons into a grafted PNS "bridge", and enter adult host targets that were partially deafferented. Embryonic eyes of E11, E14, E18 and E21 rats were sutured to peripheral nerve segments which served as bridges between the host eye and frontal cortex. Projections between the developing retina and the host brain could then be evaluated using HRP tracing techniques. From a methodological standpoint, the preparations are 65% effective; i.e., a viable bridge results between the embryonic eye and the host forebrain. The results presented in the accompanying paper demonstrate that the technique can yield results indicative of embryonic retinal development and axonal projection through the graft and into the host brain. This partial reconstruction of the visual system may prove a useful tool in understanding the uses and limitations of grafting in the CNS.
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spelling pubmed-25650062008-10-16 Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology Zanakis, Michael F. Lowe, Howard F. Jacobsen, Glenn LaCorte, Michael Lee, Simone P. Hallas, Brian H. J Neural Transplant Article Various techniques have been explored to determine the uses and limitations of techniques that enable the adult CNS to regenerate, but relatively little attention has been given to the consideration of a "reconstructed" visual system. Using this approach, one can design experiments to study the uses of exogenous tissues in reestablishing neuronal circuits that have been damaged. Toward this end, experiments were designed to determine whether embryonic retinal ganglion cells can project axons into a grafted PNS "bridge", and enter adult host targets that were partially deafferented. Embryonic eyes of E11, E14, E18 and E21 rats were sutured to peripheral nerve segments which served as bridges between the host eye and frontal cortex. Projections between the developing retina and the host brain could then be evaluated using HRP tracing techniques. From a methodological standpoint, the preparations are 65% effective; i.e., a viable bridge results between the embryonic eye and the host forebrain. The results presented in the accompanying paper demonstrate that the technique can yield results indicative of embryonic retinal development and axonal projection through the graft and into the host brain. This partial reconstruction of the visual system may prove a useful tool in understanding the uses and limitations of grafting in the CNS. Hindawi Publishing Corporation 1989 /pmc/articles/PMC2565006/ /pubmed/2485119 http://dx.doi.org/10.1155/NP.1989.77 Text en Copyright © 1989.
spellingShingle Article
Zanakis, Michael F.
Lowe, Howard F.
Jacobsen, Glenn
LaCorte, Michael
Lee, Simone P.
Hallas, Brian H.
Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title_full Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title_fullStr Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title_full_unstemmed Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title_short Developing Retina and PNS Segments for Transplantation Into the Adult Host Eye: Reconstruction of the Mammalian Visual System. 1. Methodology
title_sort developing retina and pns segments for transplantation into the adult host eye: reconstruction of the mammalian visual system. 1. methodology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565006/
https://www.ncbi.nlm.nih.gov/pubmed/2485119
http://dx.doi.org/10.1155/NP.1989.77
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