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Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates

The ability of sustained treatment of a single extraocular muscle with glial cell line-derived neurotrophic factor (GDNF) to produce a strabismus in infant non-human primates was tested. Six infant non-human primates received a pellet containing GDNF, releasing 2 µg/day for 90 days, on one medial re...

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Autores principales: Fleuriet, Jérome, Willoughby, Christy L., Kueppers, Rachel B., Mustari, Michael J., McLoon, Linda K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368047/
https://www.ncbi.nlm.nih.gov/pubmed/32681083
http://dx.doi.org/10.1038/s41598-020-68743-3
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author Fleuriet, Jérome
Willoughby, Christy L.
Kueppers, Rachel B.
Mustari, Michael J.
McLoon, Linda K.
author_facet Fleuriet, Jérome
Willoughby, Christy L.
Kueppers, Rachel B.
Mustari, Michael J.
McLoon, Linda K.
author_sort Fleuriet, Jérome
collection PubMed
description The ability of sustained treatment of a single extraocular muscle with glial cell line-derived neurotrophic factor (GDNF) to produce a strabismus in infant non-human primates was tested. Six infant non-human primates received a pellet containing GDNF, releasing 2 µg/day for 90 days, on one medial rectus muscle. Eye alignment was assessed up to 6 months. Five of the six animals showed a slow decrease in eye misalignment from the significant exotropia present at birth, ending with approximately 10° of exotropia. Controls became orthotropic. Misalignment averaged 8° three months after treatment ended. After sustained GDNF treatment, few changes were seen in mean myofiber cross-sectional areas compared to age-matched naïve controls. Neuromuscular junction number was unaltered in the medial rectus muscles, but were significantly reduced in the untreated lateral recti. Neuromuscular junctions on slow fibers became multiply innervated after this sustained GDNF treatment. Pitx2-positive cells significantly decreased in treated and contralateral medial rectus muscles. Our study suggests that balanced GDNF signaling plays a role in normal development and maintenance of orthotropia. Sustained GDNF treatment of one medial rectus muscle resulted in a measurable misalignment largely maintained 3 months after treatment ended. Structural changes suggest mechanisms for producing an imbalance in muscle function.
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spelling pubmed-73680472020-07-22 Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates Fleuriet, Jérome Willoughby, Christy L. Kueppers, Rachel B. Mustari, Michael J. McLoon, Linda K. Sci Rep Article The ability of sustained treatment of a single extraocular muscle with glial cell line-derived neurotrophic factor (GDNF) to produce a strabismus in infant non-human primates was tested. Six infant non-human primates received a pellet containing GDNF, releasing 2 µg/day for 90 days, on one medial rectus muscle. Eye alignment was assessed up to 6 months. Five of the six animals showed a slow decrease in eye misalignment from the significant exotropia present at birth, ending with approximately 10° of exotropia. Controls became orthotropic. Misalignment averaged 8° three months after treatment ended. After sustained GDNF treatment, few changes were seen in mean myofiber cross-sectional areas compared to age-matched naïve controls. Neuromuscular junction number was unaltered in the medial rectus muscles, but were significantly reduced in the untreated lateral recti. Neuromuscular junctions on slow fibers became multiply innervated after this sustained GDNF treatment. Pitx2-positive cells significantly decreased in treated and contralateral medial rectus muscles. Our study suggests that balanced GDNF signaling plays a role in normal development and maintenance of orthotropia. Sustained GDNF treatment of one medial rectus muscle resulted in a measurable misalignment largely maintained 3 months after treatment ended. Structural changes suggest mechanisms for producing an imbalance in muscle function. Nature Publishing Group UK 2020-07-17 /pmc/articles/PMC7368047/ /pubmed/32681083 http://dx.doi.org/10.1038/s41598-020-68743-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fleuriet, Jérome
Willoughby, Christy L.
Kueppers, Rachel B.
Mustari, Michael J.
McLoon, Linda K.
Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title_full Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title_fullStr Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title_full_unstemmed Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title_short Eye alignment changes caused by sustained GDNF treatment of an extraocular muscle in infant non-human primates
title_sort eye alignment changes caused by sustained gdnf treatment of an extraocular muscle in infant non-human primates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368047/
https://www.ncbi.nlm.nih.gov/pubmed/32681083
http://dx.doi.org/10.1038/s41598-020-68743-3
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