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Ciliary margin-derived BMP4 does not have a major role in ocular development

Heterozygous Bmp4 mutations in humans and mice cause severe ocular anterior segment dysgenesis (ASD). Abnormalities include pupil displacement, corneal opacity, iridocorneal adhesions, and variable intraocular pressure, as well as some retinal and vascular defects. It is presently not known what sou...

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Autores principales: Rausch, Rebecca L., Libby, Richard T., Kiernan, Amy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940228/
https://www.ncbi.nlm.nih.gov/pubmed/29738572
http://dx.doi.org/10.1371/journal.pone.0197048
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author Rausch, Rebecca L.
Libby, Richard T.
Kiernan, Amy E.
author_facet Rausch, Rebecca L.
Libby, Richard T.
Kiernan, Amy E.
author_sort Rausch, Rebecca L.
collection PubMed
description Heterozygous Bmp4 mutations in humans and mice cause severe ocular anterior segment dysgenesis (ASD). Abnormalities include pupil displacement, corneal opacity, iridocorneal adhesions, and variable intraocular pressure, as well as some retinal and vascular defects. It is presently not known what source of BMP4 is responsible for these defects, as BMP4 is expressed in several developing ocular and surrounding tissues. In particular, BMP4 is expressed in the ciliary margins of the optic cup which give rise to anterior segment structures such as the ciliary body and iris, making it a good candidate for the required source of BMP4 for anterior segment development. Here, we test whether ciliary margin-derived BMP4 is required for ocular development using two different conditional knockout approaches. In addition, we compared the conditional deletion phenotypes with Bmp4 heterozygous null mice. Morphological, molecular, and functional assays were performed on adult mutant mice, including histology, immunohistochemistry, in vivo imaging, and intraocular pressure measurements. Surprisingly, in contrast to Bmp4 heterozygous mutants, our analyses revealed that the anterior and posterior segments of Bmp4 conditional knockouts developed normally. These results indicate that ciliary margin-derived BMP4 does not have a major role in ocular development, although subtle alterations could not be ruled out. Furthermore, we demonstrated that the anterior and posterior phenotypes observed in Bmp4 heterozygous animals showed a strong propensity to co-occur, suggesting a common, non-cell autonomous source for these defects.
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spelling pubmed-59402282018-05-18 Ciliary margin-derived BMP4 does not have a major role in ocular development Rausch, Rebecca L. Libby, Richard T. Kiernan, Amy E. PLoS One Research Article Heterozygous Bmp4 mutations in humans and mice cause severe ocular anterior segment dysgenesis (ASD). Abnormalities include pupil displacement, corneal opacity, iridocorneal adhesions, and variable intraocular pressure, as well as some retinal and vascular defects. It is presently not known what source of BMP4 is responsible for these defects, as BMP4 is expressed in several developing ocular and surrounding tissues. In particular, BMP4 is expressed in the ciliary margins of the optic cup which give rise to anterior segment structures such as the ciliary body and iris, making it a good candidate for the required source of BMP4 for anterior segment development. Here, we test whether ciliary margin-derived BMP4 is required for ocular development using two different conditional knockout approaches. In addition, we compared the conditional deletion phenotypes with Bmp4 heterozygous null mice. Morphological, molecular, and functional assays were performed on adult mutant mice, including histology, immunohistochemistry, in vivo imaging, and intraocular pressure measurements. Surprisingly, in contrast to Bmp4 heterozygous mutants, our analyses revealed that the anterior and posterior segments of Bmp4 conditional knockouts developed normally. These results indicate that ciliary margin-derived BMP4 does not have a major role in ocular development, although subtle alterations could not be ruled out. Furthermore, we demonstrated that the anterior and posterior phenotypes observed in Bmp4 heterozygous animals showed a strong propensity to co-occur, suggesting a common, non-cell autonomous source for these defects. Public Library of Science 2018-05-08 /pmc/articles/PMC5940228/ /pubmed/29738572 http://dx.doi.org/10.1371/journal.pone.0197048 Text en © 2018 Rausch et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rausch, Rebecca L.
Libby, Richard T.
Kiernan, Amy E.
Ciliary margin-derived BMP4 does not have a major role in ocular development
title Ciliary margin-derived BMP4 does not have a major role in ocular development
title_full Ciliary margin-derived BMP4 does not have a major role in ocular development
title_fullStr Ciliary margin-derived BMP4 does not have a major role in ocular development
title_full_unstemmed Ciliary margin-derived BMP4 does not have a major role in ocular development
title_short Ciliary margin-derived BMP4 does not have a major role in ocular development
title_sort ciliary margin-derived bmp4 does not have a major role in ocular development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940228/
https://www.ncbi.nlm.nih.gov/pubmed/29738572
http://dx.doi.org/10.1371/journal.pone.0197048
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