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An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture.

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An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture. / Koizumi, Noriko; Cooper, Leanne J.; Fullwood, Nigel J. et al.
In: Investigative Ophthalmology and Visual Science, Vol. 43, No. 7, 2002, p. 2114-2121.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Koizumi, N, Cooper, LJ, Fullwood, NJ, Nakamura, T, Inoki, K, Tsuzuki, M & Kinoshita, S 2002, 'An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture.', Investigative Ophthalmology and Visual Science, vol. 43, no. 7, pp. 2114-2121. <http://www.iovs.org/cgi/content/abstract/43/7/2114>

APA

Koizumi, N., Cooper, L. J., Fullwood, N. J., Nakamura, T., Inoki, K., Tsuzuki, M., & Kinoshita, S. (2002). An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture. Investigative Ophthalmology and Visual Science, 43(7), 2114-2121. http://www.iovs.org/cgi/content/abstract/43/7/2114

Vancouver

Koizumi N, Cooper LJ, Fullwood NJ, Nakamura T, Inoki K, Tsuzuki M et al. An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture. Investigative Ophthalmology and Visual Science. 2002;43(7):2114-2121.

Author

Koizumi, Noriko ; Cooper, Leanne J. ; Fullwood, Nigel J. et al. / An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture. In: Investigative Ophthalmology and Visual Science. 2002 ; Vol. 43, No. 7. pp. 2114-2121.

Bibtex

@article{6b4e5b2fa3f24c71b48b4ee869888219,
title = "An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture.",
abstract = "PURPOSE. A previous report has described an ocular surface reconstruction method involving the use of cultivated corneal epithelium derived from limbal explants. In the current study, a new culture system was developed involving the in vitro propagation on amniotic membrane (AM) of epithelial cells from enzymatically dissociated limbal epithelium. The purpose of this new method is to produce a cultivated epithelial cell layer that contains stem cells and that is superior to explanted cultivated epithelium. The new cell-suspension technique was compared with the existing explant method. METHODS. Limbal epithelial cells were dissociated from donor eyes by dispase and seeded on the denuded AM. Small pieces of limbal epithelium were also cultured on denuded AM as explant cultures. The cultivated epithelium was examined by electron microscopy and immunohistochemistry for cornea-specific keratins (K3 and K12). RESULTS. Both cell-suspension and explant culture methods produced a healthy epithelial cell layer. The cell-suspension culture had significantly (P < 0.001) more desmosomal junctions between the explant-cultured basal cells. In addition, the intercellular spaces between the cell-suspension{\textquoteright}s basal cells were significantly (P < 0.001) smaller than those between the explant-cultured basal cells. Both types of cultivated epithelium showed positive expression of K3 and K12 keratins. In the cell-suspension culture, expression of K3 and K12 keratins was more prominent in the superficial cells. CONCLUSIONS. Corneal epithelial cells were successfully regenerated in vitro by a cell-suspension culture system. The suspension-cultured epithelium must include some stem cells and morphologically is significantly superior to explant-cultured epithelium. Thus, this new technique is potentially more suitable for cultivated corneal limbal epithelial transplantation.",
author = "Noriko Koizumi and Cooper, {Leanne J.} and Fullwood, {Nigel J.} and Takahiro Nakamura and Keiko Inoki and Masakatsu Tsuzuki and Shigeru Kinoshita",
year = "2002",
language = "English",
volume = "43",
pages = "2114--2121",
journal = "Investigative Ophthalmology and Visual Science",
issn = "1552-5783",
publisher = "ASSOC RESEARCH VISION OPHTHALMOLOGY INC",
number = "7",

}

RIS

TY - JOUR

T1 - An Evaluation of Cultivated Corneal Limbal Epithelial Cells, Using Cell-Suspension Culture.

AU - Koizumi, Noriko

AU - Cooper, Leanne J.

AU - Fullwood, Nigel J.

AU - Nakamura, Takahiro

AU - Inoki, Keiko

AU - Tsuzuki, Masakatsu

AU - Kinoshita, Shigeru

PY - 2002

Y1 - 2002

N2 - PURPOSE. A previous report has described an ocular surface reconstruction method involving the use of cultivated corneal epithelium derived from limbal explants. In the current study, a new culture system was developed involving the in vitro propagation on amniotic membrane (AM) of epithelial cells from enzymatically dissociated limbal epithelium. The purpose of this new method is to produce a cultivated epithelial cell layer that contains stem cells and that is superior to explanted cultivated epithelium. The new cell-suspension technique was compared with the existing explant method. METHODS. Limbal epithelial cells were dissociated from donor eyes by dispase and seeded on the denuded AM. Small pieces of limbal epithelium were also cultured on denuded AM as explant cultures. The cultivated epithelium was examined by electron microscopy and immunohistochemistry for cornea-specific keratins (K3 and K12). RESULTS. Both cell-suspension and explant culture methods produced a healthy epithelial cell layer. The cell-suspension culture had significantly (P < 0.001) more desmosomal junctions between the explant-cultured basal cells. In addition, the intercellular spaces between the cell-suspension’s basal cells were significantly (P < 0.001) smaller than those between the explant-cultured basal cells. Both types of cultivated epithelium showed positive expression of K3 and K12 keratins. In the cell-suspension culture, expression of K3 and K12 keratins was more prominent in the superficial cells. CONCLUSIONS. Corneal epithelial cells were successfully regenerated in vitro by a cell-suspension culture system. The suspension-cultured epithelium must include some stem cells and morphologically is significantly superior to explant-cultured epithelium. Thus, this new technique is potentially more suitable for cultivated corneal limbal epithelial transplantation.

AB - PURPOSE. A previous report has described an ocular surface reconstruction method involving the use of cultivated corneal epithelium derived from limbal explants. In the current study, a new culture system was developed involving the in vitro propagation on amniotic membrane (AM) of epithelial cells from enzymatically dissociated limbal epithelium. The purpose of this new method is to produce a cultivated epithelial cell layer that contains stem cells and that is superior to explanted cultivated epithelium. The new cell-suspension technique was compared with the existing explant method. METHODS. Limbal epithelial cells were dissociated from donor eyes by dispase and seeded on the denuded AM. Small pieces of limbal epithelium were also cultured on denuded AM as explant cultures. The cultivated epithelium was examined by electron microscopy and immunohistochemistry for cornea-specific keratins (K3 and K12). RESULTS. Both cell-suspension and explant culture methods produced a healthy epithelial cell layer. The cell-suspension culture had significantly (P < 0.001) more desmosomal junctions between the explant-cultured basal cells. In addition, the intercellular spaces between the cell-suspension’s basal cells were significantly (P < 0.001) smaller than those between the explant-cultured basal cells. Both types of cultivated epithelium showed positive expression of K3 and K12 keratins. In the cell-suspension culture, expression of K3 and K12 keratins was more prominent in the superficial cells. CONCLUSIONS. Corneal epithelial cells were successfully regenerated in vitro by a cell-suspension culture system. The suspension-cultured epithelium must include some stem cells and morphologically is significantly superior to explant-cultured epithelium. Thus, this new technique is potentially more suitable for cultivated corneal limbal epithelial transplantation.

M3 - Journal article

VL - 43

SP - 2114

EP - 2121

JO - Investigative Ophthalmology and Visual Science

JF - Investigative Ophthalmology and Visual Science

SN - 1552-5783

IS - 7

ER -