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The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane.

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The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane. / Nakamura, Takahiro; Endo, Ken-Ichi; Cooper, Leanne J. et al.
In: Investigative Ophthalmology and Visual Science, Vol. 44, 2003, p. 106-116.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Nakamura, T, Endo, K-I, Cooper, LJ, Fullwood, NJ, Tanifuji, N, Tsuzuki, M, Koizumi, N, Inatomi, T, Sano, Y & Kinoshita, S 2003, 'The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane.', Investigative Ophthalmology and Visual Science, vol. 44, pp. 106-116. https://doi.org/10.1167/iovs.02-0195

APA

Nakamura, T., Endo, K.-I., Cooper, L. J., Fullwood, N. J., Tanifuji, N., Tsuzuki, M., Koizumi, N., Inatomi, T., Sano, Y., & Kinoshita, S. (2003). The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane. Investigative Ophthalmology and Visual Science, 44, 106-116. https://doi.org/10.1167/iovs.02-0195

Vancouver

Nakamura T, Endo KI, Cooper LJ, Fullwood NJ, Tanifuji N, Tsuzuki M et al. The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane. Investigative Ophthalmology and Visual Science. 2003;44:106-116. doi: 10.1167/iovs.02-0195

Author

Nakamura, Takahiro ; Endo, Ken-Ichi ; Cooper, Leanne J. et al. / The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane. In: Investigative Ophthalmology and Visual Science. 2003 ; Vol. 44. pp. 106-116.

Bibtex

@article{7bb9b5c359e04a418131c73c3e22c8c6,
title = "The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane.",
abstract = "PURPOSE. To determine the feasibility of using human amniotic membrane (AM) as a substrate for culturing oral epithelial cells and to investigate the possibility of using autologous cultivated oral epithelial cells in ocular surface reconstruction. METHODS. An ocular surface injury was created in one eye of each of eight adult albino rabbits by a lamellar keratectomy, and a conjunctival excision was performed, including and extending 5 mm outside the limbus. Oral mucosal biopsy specimens were obtained from these eight adult albino rabbits and cultivated for 3 weeks on a denuded AM carrier. The cultivated epithelium was examined by electron microscopy (EM) and immunohistochemically labeled for several keratins. At 3 to 4 weeks after the ocular surface injury, the conjunctivalized corneal surfaces of the eight rabbits were surgically reconstructed by transplanting the autologous cultivated oral epithelial cells on the AM carrier. RESULTS. The cultivated oral epithelial sheet had four to five layers of stratified, well-differentiated cells. EM revealed that the epithelial cells were very similar in appearance to those of normal corneal epithelium, had numerous desmosomal junctions, and were attached to a basement membrane with hemidesmosomes. Immunohistochemistry confirmed the presence of the keratin pair 4 and 13 and keratin-3 in the cultivated oral epithelial cells. Corneas that were grafted with the cultivated oral epithelial cells on an AM carrier were clear and were all epithelialized 10 days after surgery. CONCLUSIONS. Cultures of oral epithelial cells can be generated to confluence on AM expanded ex vivo from biopsy-derived oral mucosal tissue. Autologous transplantation was performed with these cultivated oral epithelial cells onto the ocular surfaces of keratectomized rabbit eyes. Autologous transplantation of cultivated oral epithelium is a feasible method for ocular surface reconstruction. The long-term outcome of such transplantation is not yet clear, and its feasibility in clinical use should be evaluated further.",
author = "Takahiro Nakamura and Ken-Ichi Endo and Cooper, {Leanne J.} and Fullwood, {Nigel J.} and Noriko Tanifuji and Masakatsu Tsuzuki and Noriko Koizumi and Tsutomu Inatomi and Yoichiro Sano and Shigeru Kinoshita",
year = "2003",
doi = "10.1167/iovs.02-0195",
language = "English",
volume = "44",
pages = "106--116",
journal = "Investigative Ophthalmology and Visual Science",
issn = "1552-5783",
publisher = "ASSOC RESEARCH VISION OPHTHALMOLOGY INC",

}

RIS

TY - JOUR

T1 - The successful culture and autologous transplantation of rabbit oral mucosal epithelial cells on amniotic membrane.

AU - Nakamura, Takahiro

AU - Endo, Ken-Ichi

AU - Cooper, Leanne J.

AU - Fullwood, Nigel J.

AU - Tanifuji, Noriko

AU - Tsuzuki, Masakatsu

AU - Koizumi, Noriko

AU - Inatomi, Tsutomu

AU - Sano, Yoichiro

AU - Kinoshita, Shigeru

PY - 2003

Y1 - 2003

N2 - PURPOSE. To determine the feasibility of using human amniotic membrane (AM) as a substrate for culturing oral epithelial cells and to investigate the possibility of using autologous cultivated oral epithelial cells in ocular surface reconstruction. METHODS. An ocular surface injury was created in one eye of each of eight adult albino rabbits by a lamellar keratectomy, and a conjunctival excision was performed, including and extending 5 mm outside the limbus. Oral mucosal biopsy specimens were obtained from these eight adult albino rabbits and cultivated for 3 weeks on a denuded AM carrier. The cultivated epithelium was examined by electron microscopy (EM) and immunohistochemically labeled for several keratins. At 3 to 4 weeks after the ocular surface injury, the conjunctivalized corneal surfaces of the eight rabbits were surgically reconstructed by transplanting the autologous cultivated oral epithelial cells on the AM carrier. RESULTS. The cultivated oral epithelial sheet had four to five layers of stratified, well-differentiated cells. EM revealed that the epithelial cells were very similar in appearance to those of normal corneal epithelium, had numerous desmosomal junctions, and were attached to a basement membrane with hemidesmosomes. Immunohistochemistry confirmed the presence of the keratin pair 4 and 13 and keratin-3 in the cultivated oral epithelial cells. Corneas that were grafted with the cultivated oral epithelial cells on an AM carrier were clear and were all epithelialized 10 days after surgery. CONCLUSIONS. Cultures of oral epithelial cells can be generated to confluence on AM expanded ex vivo from biopsy-derived oral mucosal tissue. Autologous transplantation was performed with these cultivated oral epithelial cells onto the ocular surfaces of keratectomized rabbit eyes. Autologous transplantation of cultivated oral epithelium is a feasible method for ocular surface reconstruction. The long-term outcome of such transplantation is not yet clear, and its feasibility in clinical use should be evaluated further.

AB - PURPOSE. To determine the feasibility of using human amniotic membrane (AM) as a substrate for culturing oral epithelial cells and to investigate the possibility of using autologous cultivated oral epithelial cells in ocular surface reconstruction. METHODS. An ocular surface injury was created in one eye of each of eight adult albino rabbits by a lamellar keratectomy, and a conjunctival excision was performed, including and extending 5 mm outside the limbus. Oral mucosal biopsy specimens were obtained from these eight adult albino rabbits and cultivated for 3 weeks on a denuded AM carrier. The cultivated epithelium was examined by electron microscopy (EM) and immunohistochemically labeled for several keratins. At 3 to 4 weeks after the ocular surface injury, the conjunctivalized corneal surfaces of the eight rabbits were surgically reconstructed by transplanting the autologous cultivated oral epithelial cells on the AM carrier. RESULTS. The cultivated oral epithelial sheet had four to five layers of stratified, well-differentiated cells. EM revealed that the epithelial cells were very similar in appearance to those of normal corneal epithelium, had numerous desmosomal junctions, and were attached to a basement membrane with hemidesmosomes. Immunohistochemistry confirmed the presence of the keratin pair 4 and 13 and keratin-3 in the cultivated oral epithelial cells. Corneas that were grafted with the cultivated oral epithelial cells on an AM carrier were clear and were all epithelialized 10 days after surgery. CONCLUSIONS. Cultures of oral epithelial cells can be generated to confluence on AM expanded ex vivo from biopsy-derived oral mucosal tissue. Autologous transplantation was performed with these cultivated oral epithelial cells onto the ocular surfaces of keratectomized rabbit eyes. Autologous transplantation of cultivated oral epithelium is a feasible method for ocular surface reconstruction. The long-term outcome of such transplantation is not yet clear, and its feasibility in clinical use should be evaluated further.

U2 - 10.1167/iovs.02-0195

DO - 10.1167/iovs.02-0195

M3 - Journal article

VL - 44

SP - 106

EP - 116

JO - Investigative Ophthalmology and Visual Science

JF - Investigative Ophthalmology and Visual Science

SN - 1552-5783

ER -