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Original Article
131 (
3
); 422-428
doi:
10.25259/IJMR_20101313_422

Culture & characterisation of limbal epithelial cells & oral mucosal cells

L & T Department of Ocular Pathology, Vision Research Foundation, Sankara Nethralaya, India
Department of Cornea Services Medical Research Foundation, Sankara Nethralaya, India

Reprint requests: Dr Subramanian Krishnakumar, Department of Ocular Pathology, Vision Research Foundation, Sankara Nethralaya 18 College Road, Chennai 600 006, India e-mail: drkrishnakumar_2000@yahoo.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background & objectives:

Sources of autologous tissue that can functionally replace the corneal epithelium have been considered as an alternative to allogenous limbal transplants for limbal stem cells deficiency (LSCD). The aim of the present study was to compare the characterization of oral mucosa with limbal epithelial cells by markers using reverse transcriptase polymerase chain reaction (RT-PCR).

Methods:

Experiments were performed using oral tissue (n=6) obtained from patients who underwent oral mucosal graft for LSCD. Confluent cultures of limbus and oral mucosa epithelial cells were characterized by the pututative stem cell markers using RT-PCR. The morphological characteristics of cultivated epithelial cells were analyzed by haematoxylin and eosin staining and phase contrast microscopy.

Results:

Confluent sheets of epithelial cells were seen at the end of 14th day resembling the morphological features of limbal epithelia. RT–PCR analysis showed that cultured oral epithelial cells expressed markers such as ABCG2, p63, delta Np63, isoforms of p63, Keratin 3 (K3), membrane protein – Mucin (MUC 1, 4 and 16) and Antimicrobial Peptide - AMP (Human β Defensin – hBD 1, 2 and 3).

Interpretation & conclusions:

Oral epithelial cultures have morphological features resembling corneal and limbal epithelial cells by expressing similar marker genes. Thus, feasibility of clinical use of oral epithelial cells need be evaluated for allogenous limbal transplants.

Keywords

Antimicrobial peptide
bilateral limbal stem cell deficiency
corneal stem cell markers
limbal stem cell markers
mucin
oral mucosa
p63 isoforms

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