Human sclera maintains common characteristics with cartilage throughout evolution.

<h4>Background</h4>The sclera maintains and protects the eye ball, which receives visual inputs. Although the sclera does not contribute significantly to visual perception, scleral diseases such as refractory scleritis, scleral perforation and pathological myopia are considered incurable...

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Autores principales: Yuko Seko, Noriyuki Azuma, Yoriko Takahashi, Hatsune Makino, Toshiyuki Morito, Takeshi Muneta, Kenji Matsumoto, Hirohisa Saito, Ichiro Sekiya, Akihiro Umezawa
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Publicado: Public Library of Science (PLoS) 2008
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spelling oai:doaj.org-article:653d3995be674c53a112a33afe07946a2021-11-25T06:18:33ZHuman sclera maintains common characteristics with cartilage throughout evolution.1932-620310.1371/journal.pone.0003709https://doaj.org/article/653d3995be674c53a112a33afe07946a2008-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19002264/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The sclera maintains and protects the eye ball, which receives visual inputs. Although the sclera does not contribute significantly to visual perception, scleral diseases such as refractory scleritis, scleral perforation and pathological myopia are considered incurable or difficult to cure. The aim of this study is to identify characteristics of the human sclera as one of the connective tissues derived from the neural crest and mesoderm.<h4>Methodology/principal findings</h4>We have demonstrated microarray data of cultured human infant scleral cells. Hierarchical clustering was performed to group scleral cells and other mesenchymal cells into subcategories. Hierarchical clustering analysis showed similarity between scleral cells and auricular cartilage-derived cells. Cultured micromasses of scleral cells exposed to TGF-betas and BMP2 produced an abundant matrix. The expression of cartilage-associated genes, such as Indian hedge hog, type X collagen, and MMP13, was up-regulated within 3 weeks in vitro. These results suggest that human 'sclera'-derived cells can be considered chondrocytes when cultured ex vivo.<h4>Conclusions/significance</h4>Our present study shows a chondrogenic potential of human sclera. Interestingly, the sclera of certain vertebrates, such as birds and fish, is composed of hyaline cartilage. Although the human sclera is not a cartilaginous tissue, the human sclera maintains chondrogenic potential throughout evolution. In addition, our findings directly explain an enigma that the sclera and the joint cartilage are common targets of inflammatory cells in rheumatic arthritis. The present global gene expression database will contribute to the clarification of the pathogenesis of developmental diseases such as high myopia.Yuko SekoNoriyuki AzumaYoriko TakahashiHatsune MakinoToshiyuki MoritoTakeshi MunetaKenji MatsumotoHirohisa SaitoIchiro SekiyaAkihiro UmezawaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 3, Iss 11, p e3709 (2008)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yuko Seko
Noriyuki Azuma
Yoriko Takahashi
Hatsune Makino
Toshiyuki Morito
Takeshi Muneta
Kenji Matsumoto
Hirohisa Saito
Ichiro Sekiya
Akihiro Umezawa
Human sclera maintains common characteristics with cartilage throughout evolution.
description <h4>Background</h4>The sclera maintains and protects the eye ball, which receives visual inputs. Although the sclera does not contribute significantly to visual perception, scleral diseases such as refractory scleritis, scleral perforation and pathological myopia are considered incurable or difficult to cure. The aim of this study is to identify characteristics of the human sclera as one of the connective tissues derived from the neural crest and mesoderm.<h4>Methodology/principal findings</h4>We have demonstrated microarray data of cultured human infant scleral cells. Hierarchical clustering was performed to group scleral cells and other mesenchymal cells into subcategories. Hierarchical clustering analysis showed similarity between scleral cells and auricular cartilage-derived cells. Cultured micromasses of scleral cells exposed to TGF-betas and BMP2 produced an abundant matrix. The expression of cartilage-associated genes, such as Indian hedge hog, type X collagen, and MMP13, was up-regulated within 3 weeks in vitro. These results suggest that human 'sclera'-derived cells can be considered chondrocytes when cultured ex vivo.<h4>Conclusions/significance</h4>Our present study shows a chondrogenic potential of human sclera. Interestingly, the sclera of certain vertebrates, such as birds and fish, is composed of hyaline cartilage. Although the human sclera is not a cartilaginous tissue, the human sclera maintains chondrogenic potential throughout evolution. In addition, our findings directly explain an enigma that the sclera and the joint cartilage are common targets of inflammatory cells in rheumatic arthritis. The present global gene expression database will contribute to the clarification of the pathogenesis of developmental diseases such as high myopia.
format article
author Yuko Seko
Noriyuki Azuma
Yoriko Takahashi
Hatsune Makino
Toshiyuki Morito
Takeshi Muneta
Kenji Matsumoto
Hirohisa Saito
Ichiro Sekiya
Akihiro Umezawa
author_facet Yuko Seko
Noriyuki Azuma
Yoriko Takahashi
Hatsune Makino
Toshiyuki Morito
Takeshi Muneta
Kenji Matsumoto
Hirohisa Saito
Ichiro Sekiya
Akihiro Umezawa
author_sort Yuko Seko
title Human sclera maintains common characteristics with cartilage throughout evolution.
title_short Human sclera maintains common characteristics with cartilage throughout evolution.
title_full Human sclera maintains common characteristics with cartilage throughout evolution.
title_fullStr Human sclera maintains common characteristics with cartilage throughout evolution.
title_full_unstemmed Human sclera maintains common characteristics with cartilage throughout evolution.
title_sort human sclera maintains common characteristics with cartilage throughout evolution.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/653d3995be674c53a112a33afe07946a
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