TY - JOUR
T1 - Remodeling of epithelial cells and basement membranes in a corneal deficiency model with long-term follow-up
AU - Kameishi, Sumako
AU - Sugiyama, Hiroaki
AU - Yamato, Masayuki
AU - Sado, Yoshikazu
AU - Namiki, Hideo
AU - Kato, Takashi
AU - Okano, Teruo
N1 - Funding Information:
Dr Teruo Okano is a founder and director of the board of CellSeed Inc., licensing technologies and patents from Tokyo Women’s Medical University. Dr Teruo Okano and Dr Masayuki Yamato are shareholders of CellSeed Inc. Tokyo Women’s Medical University receives research funding from CellSeed Inc.
Funding Information:
We thank Dr Norio Ueno, Dr Ryo Takagi, Mr Daisuke Murakami, and Dr Makoto Kondo (Tokyo Women’s Medical University) for their useful comments and technical criticism. This study was partially supported by a Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Fellows, Creation of innovation centers for advanced interdisciplinary research areas Program in the Project for Developing Innovation Systems ‘Cell Sheet Tissue Engineering Center (CSTEC)’ from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan and the Global COE program, the Multidisciplinary Education and Research Center for Regenerative Medicine (MERCREM) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan and Grant-in-Aid for Scientific Research on Innovative Areas ‘Hyper Bio Assembler for 3D Cellular Innovation’, Japan.
Publisher Copyright:
© 2015 USCAP, Inc All rights reserved.
PY - 2015/3/3
Y1 - 2015/3/3
N2 - The ocular surface consists of the cornea, conjunctiva, and the limbus that is located in the transitional zone between the cornea and conjunctiva. The corneal epithelial cells are generated through the mitosis of corneal epithelial stem cells in the limbus. This study investigated a rabbit corneal deficiency model prepared by the surgical removal of the corneal and limbal epithelia, which express cytokeratin 12 (K12). After the surgery, K13-expressing conjunctival epithelium migrated onto the corneal surface and completely covered the surface, leading to neovascularization and corneal opacification. However, at 24 and 48 weeks after the surgery, K12-expressing cornea-like cells reappeared on the model ocular surface. These cells formed an island surrounded by invaded conjunctiva and were isolated from the limbus. Interestingly, in the 24-week model surface, α1(IV) and α2(IV) collagen chains, which are normally found in the basement membrane of the native limbus and conjunctiva, and not in the cornea, were continuously deposited throughout the entire basement membrane, including the basement membrane under cornea-like cells. By contrast, in the 48-week model surface, α1(IV) and α2(IV) collagen chains were absent from the basement membrane beneath the central part of cornea-like cells and were localized below the invaded conjunctiva and the transitional zone between cornea-like cells and the invaded conjunctiva, which had similar distribution to the native ocular basement membrane. Moreover, K12, K14, p63, vimentin, and α1(IV) and α2(IV) collagen chains, which are colocalized in the native limbus, were all present at the transitional zone of the 48-week model surface. Therefore, a limbus-like structure appeared to be reconstructed on the surface of the 48-week model as a stem cell niche. This study should aid in the understanding of human corneal deficiency, the correlation between the epithelial cell phenotype and the composition of the basement membrane, and the epithelial stem cell niche.
AB - The ocular surface consists of the cornea, conjunctiva, and the limbus that is located in the transitional zone between the cornea and conjunctiva. The corneal epithelial cells are generated through the mitosis of corneal epithelial stem cells in the limbus. This study investigated a rabbit corneal deficiency model prepared by the surgical removal of the corneal and limbal epithelia, which express cytokeratin 12 (K12). After the surgery, K13-expressing conjunctival epithelium migrated onto the corneal surface and completely covered the surface, leading to neovascularization and corneal opacification. However, at 24 and 48 weeks after the surgery, K12-expressing cornea-like cells reappeared on the model ocular surface. These cells formed an island surrounded by invaded conjunctiva and were isolated from the limbus. Interestingly, in the 24-week model surface, α1(IV) and α2(IV) collagen chains, which are normally found in the basement membrane of the native limbus and conjunctiva, and not in the cornea, were continuously deposited throughout the entire basement membrane, including the basement membrane under cornea-like cells. By contrast, in the 48-week model surface, α1(IV) and α2(IV) collagen chains were absent from the basement membrane beneath the central part of cornea-like cells and were localized below the invaded conjunctiva and the transitional zone between cornea-like cells and the invaded conjunctiva, which had similar distribution to the native ocular basement membrane. Moreover, K12, K14, p63, vimentin, and α1(IV) and α2(IV) collagen chains, which are colocalized in the native limbus, were all present at the transitional zone of the 48-week model surface. Therefore, a limbus-like structure appeared to be reconstructed on the surface of the 48-week model as a stem cell niche. This study should aid in the understanding of human corneal deficiency, the correlation between the epithelial cell phenotype and the composition of the basement membrane, and the epithelial stem cell niche.
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U2 - 10.1038/labinvest.2014.146
DO - 10.1038/labinvest.2014.146
M3 - Article
C2 - 25531563
AN - SCOPUS:84921892723
SN - 0023-6837
VL - 95
SP - 168
EP - 179
JO - Laboratory Investigation
JF - Laboratory Investigation
IS - 2
ER -