Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.

Simple limbal epithelial transplantation (SLET) and cultivated limbal epithelial transplantation (CLET) are proven clinical techniques for treating limbal stem cell deficiency (LSCD). However, the ideal size and number of the limbal explants required for transplantation has not been clearly elucidat...

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Main Authors: Abhinav Reddy Kethiri, Sayan Basu, Sachin Shukla, Virender Singh Sangwan, Vivek Singh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5619808?pdf=render
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spelling doaj-5a8ff2432592496d9d043688a35cd3db2020-11-24T21:45:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01129e018562310.1371/journal.pone.0185623Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.Abhinav Reddy KethiriSayan BasuSachin ShuklaVirender Singh SangwanVivek SinghSimple limbal epithelial transplantation (SLET) and cultivated limbal epithelial transplantation (CLET) are proven clinical techniques for treating limbal stem cell deficiency (LSCD). However, the ideal size and number of the limbal explants required for transplantation has not been clearly elucidated. This in vitro study aimed to determine the optimal limbal explant size required for complete corneal epithelialization by characterizing the cell expansion.Limbal explants obtained from both live and cadaveric biopsies were cultured on the denuded amniotic membrane. Explant size and the explant cell outgrowth (expansion) were measured using ImageJ software with respect to days. Cultures were characterized by assessing the rate of proliferation of cells with 5-bromo-2'-deoxyuridine (BrdU) assay along with the expression of different stem cell markers (ABCG2, p63α), corneal epithelial (CK3+12) and adherens junction molecules (E-Cadherin) by immunofluorescence.Explants from live biopsies had 80% growth potential in vitro whereas 40% of the cadaveric tissue failed to grow. Minimum explant sizes of 0.3 mm2 for live and ≥0.5 mm2 for cadaveric tissue had a mean expansion areas of 182.39±17.06 mm2 and 217.59±16.91 mm2 respectively suggesting adequate growth potential of the explants. Mean total percentage of proliferative cells was 31.80±3.81 in live and 33.49±4.25 in cadaveric tissue expansion. The expression was noted to be similar in cells cultured from cadaveric compared to cells cultured from live limbal tissue with respect to ABCG2, p63α, CK(3+12) and E-cadherin.Our findings show that a minimal amount of 0.3 mm2 live tissue would be sufficient for ample limbal cell expansion in vitro. Cadaveric explants <0.5 mm2 had poor growth potential. However, larger explants (≥ 0.5 mm2) had growth rate and proliferative potential similar to the live tissue. These findings could prove to be critical for clinical success especially while attempting cadaveric limbal transplantation. This study provides a novel clinical strategy for enhancing efficacy of the limbal transplantation surgery and opens the probability of even using the cadaveric tissue by considering the size of explant.http://europepmc.org/articles/PMC5619808?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Abhinav Reddy Kethiri
Sayan Basu
Sachin Shukla
Virender Singh Sangwan
Vivek Singh
spellingShingle Abhinav Reddy Kethiri
Sayan Basu
Sachin Shukla
Virender Singh Sangwan
Vivek Singh
Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
PLoS ONE
author_facet Abhinav Reddy Kethiri
Sayan Basu
Sachin Shukla
Virender Singh Sangwan
Vivek Singh
author_sort Abhinav Reddy Kethiri
title Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
title_short Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
title_full Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
title_fullStr Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
title_full_unstemmed Optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: An in vitro study.
title_sort optimizing the role of limbal explant size and source in determining the outcomes of limbal transplantation: an in vitro study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Simple limbal epithelial transplantation (SLET) and cultivated limbal epithelial transplantation (CLET) are proven clinical techniques for treating limbal stem cell deficiency (LSCD). However, the ideal size and number of the limbal explants required for transplantation has not been clearly elucidated. This in vitro study aimed to determine the optimal limbal explant size required for complete corneal epithelialization by characterizing the cell expansion.Limbal explants obtained from both live and cadaveric biopsies were cultured on the denuded amniotic membrane. Explant size and the explant cell outgrowth (expansion) were measured using ImageJ software with respect to days. Cultures were characterized by assessing the rate of proliferation of cells with 5-bromo-2'-deoxyuridine (BrdU) assay along with the expression of different stem cell markers (ABCG2, p63α), corneal epithelial (CK3+12) and adherens junction molecules (E-Cadherin) by immunofluorescence.Explants from live biopsies had 80% growth potential in vitro whereas 40% of the cadaveric tissue failed to grow. Minimum explant sizes of 0.3 mm2 for live and ≥0.5 mm2 for cadaveric tissue had a mean expansion areas of 182.39±17.06 mm2 and 217.59±16.91 mm2 respectively suggesting adequate growth potential of the explants. Mean total percentage of proliferative cells was 31.80±3.81 in live and 33.49±4.25 in cadaveric tissue expansion. The expression was noted to be similar in cells cultured from cadaveric compared to cells cultured from live limbal tissue with respect to ABCG2, p63α, CK(3+12) and E-cadherin.Our findings show that a minimal amount of 0.3 mm2 live tissue would be sufficient for ample limbal cell expansion in vitro. Cadaveric explants <0.5 mm2 had poor growth potential. However, larger explants (≥ 0.5 mm2) had growth rate and proliferative potential similar to the live tissue. These findings could prove to be critical for clinical success especially while attempting cadaveric limbal transplantation. This study provides a novel clinical strategy for enhancing efficacy of the limbal transplantation surgery and opens the probability of even using the cadaveric tissue by considering the size of explant.
url http://europepmc.org/articles/PMC5619808?pdf=render
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