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Co-Culturing Improves Induction of Human Amniotic Epithelial Cells into Corneal Epithelial-Like Cells in Vitro
Co-culture system has the feasibility of trans differentiating multipotential cells into specific cells, which plays an important role in tissue engineering. Corneal alkali burn is a common type of ocular injury, which often results in extensive damage and permanent visual impairment. Recently, human amniotic epithelial cells (hAECs), a type of multipotent cells originally isolated from amnion tissues, have become a promising source for the treatment of corneal chemical burn. Accumulating evidence has indicated that hAECs possess multi-differentiational properties for tissue repair and regeneration. Here, we present evidence that hAECs possess immunophenotypic features of corneal epithelial cells and ultrastructure changes, indicating that these cells have the potential to differentiate into corneal epithelial-like cells. Our findings therefore suggest that hAECs could be a promising substitute for corneal epithelial cells which are widely damaged by alkali burns.
Keywords
Corneal Epithelial-Like Cells, Co-Culture, Corneal Alkali Burn, Human Amniotic Epithelial Cells.
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- Saika, S. et al., Effect of overexpression of PPAR on the healing process of corneal alkali burn in mice. Am. J. Physiol., 2007, 293, 75–86.
- Arentsen, J. J., Corneal transplant allograft reaction: possible predisposing factors. Trans. Am. Ophthalmol. Soc., 1983, 81, 361– 402.
- Volker-Dieben, H. J., D’Amaro, J. and Kok-van Alphen, C. C., Hierarchy of prognostic factors for corneal allograft survival. Aust. N.Z. J. Ophthalmal., 1987, 15, 11–18.
- Atkinson, T. J., Cystic fibrosis, vector-mediated gene therapy, and relevance of toll-like receptors: a review of problems, progress, and possibilities. Curr. Gene Ther., 2008, 8, 201–207.
- Niknejad, H., Deihim, T., Peirovi, H. and Abolghasemi, H., Serum-free cryopreservation of human amniotic epithelial cells before and after isolation from their natural scaffold. Cryobiology, 2013, 67, 56–63.
- Ilancheran, S., Michalska, A., Peh, G., Wallace, E. M., Pera, M. and Manuelpillai, U., Stem cells derived from human fetal membranes display multilineage differentiation potential. Biol. Reprod., 2007, 77, 577–588.
- Zuk, P. A. et al., Multilineage cells from human adipose tissue: implications for cell-based therapies. Tissue Eng. Tissue Eng., 2001, 7, 211–228.
- Miki, T., Lehmann, T., Cai, H., Stolz, D. B. and Strom, S. C., Stem cell characteristics of amniotic epithelial cells. Stem Cells, 2005, 23, 1549–1559.
- Hou, Y., Huang, Q., Liu, T. and Guo, L., Human amnion epithelial cells can be induced to differentiate into functional insulinproducing cells. Acta Biochim. Biophys. Sci., 2008, 40, 830– 839.
- Evron, A., Goldman, S. and Shalev, E., Human amniotic epithelial cells differentiate into cells expressing germ cell specific markers when cultured in medium containing serum substitute supplement. Reprod. Biol. Endocrinol., 2012, 10, 108.
- Kim, J. S., Kim, J. C., Na, B. K., Jeong, J. M. and Song, C. Y., Amniotic membrane patching promotes healing and inhibits proteinase activity on wound healing following acute corneal alkali burn. Exp. Eye Res., 2000, 70, 329–337.
- Yao, L. et al., Role of mesenchymal stem cells on cornea wound healing induced by acute alkali burn. PLoS ONE, 2012, 7, 1–7.
- Jiang, T. S., Cai, L., Ji, W. Y., Hui, Y. N., Wang, Y. S., Hu, D. and Zhu, J., Reconstruction of the corneal epithelium with induced marrow mesenchymal stem cells in rats. Mol. Vis., 2010, 16, 1304–1316.
- Hanson, C. et al., Transplantation of human embryonic stem cells onto a partially wounded human cornea in vitro. Acta Ophthalmol., 2013, 91, 127–130.
- Lin, K.-J. et al., Topical administration of orbital fat-derived stem cells promotes corneal tissue regeneration. Stem Cell Res. Ther., 2013, 4, 72.
- Parolini, O. et al., Concise review: isolation and characterization of cells from human term placenta: outcome of the first international workshop on placenta derived stem cells. Stem Cells, 2008, 26, 300–311.
- Sheppard, D. N. and Welsh, M. J., Structure and function of the CFTR chloride channel. Physiol. Rev., 1999, 79, 23–45.
- Toshio, M., Amnion-derived stem cells: in quest of clinical applications. Stem Cell Res. Ther., 2011, 2(3), 25.
- Li, H., Niederkorn, J. Y., Neelam, S., Mayhew, E., Word, R. A., McCulley, J. P. and Alizadeh, H., Immunosuppressive factors secreted by human amniotic epithelial cells. Invest. Ophthalmol. Vis. Sci., 2005, 46, 900–907.
- Lindvall, O. and Kokaia, Z., Recovery and rehabilitation in stroke: stem cells. Stroke, 2004, 35, 2691–2694.
- Meisel, C. and Meisel, A., Suppressing immunosuppression after stroke. N. Engl. J. Med., 2011, 365, 2134–2136.
- Moodley, Y. et al., Human amnion epithelial cell transplantation abrogates lung fibrosis and augments repair. Am. J. Respir. Crit. Care Med., 2010, 182, 643–651.
- Murphy, S., Lim, R., Dickinson, H., Acharya, R., Rosli, S., Jenkin, G. and Wallace, E., Human amnion epithelial cells prevent bleomycin-induced lung injury and preserve lung function. Cell Transplant., 2011, 20, 909–923.
- Broughton, B. R., Lim, R., Arumugam, T. V., Drummond, G. R., Wallace, E. M. and Sobey, C. G., Post-stroke inflammation and the potential efficacy of novel stem cell therapies: focus on amnion epithelial cells. Front Cell Neurosci., 2013, 6, 66.
- Meng, X. T., Chen, D., Dong, Z. Y. and Liu, J. M., Enhanced neural differentiation of neural stem cells and neurite growth by amniotic epithelial cell co-culture. Cell Biol. Int., 2007, 31, 691–698.
- Venkatachalam, S., Palaniappan, T., Jayapal, P. K., Neelamegan, S., Rajan, S. S. and Muthiah, V. P., Novel neurotrophic factor secreted by amniotic epithelial cells. Biocell, 2009, 33, 81– 89.
- Chen, Y. T. et al., Human amniotic epithelial cells as novel feeder layers for promoting ex vivo expansion of limbal epithelial progenitor cells. Stem Cells, 2007, 25, 1995–2005.
- Kinoshita, S., Adachi, W., Sotozono, C., Nishida, K., Yokoi, N., Quantock, A. J. and Okubo, K., Characteristics of the human ocular surface epithelium. Prog. Retin. Eye Res., 2001, 20, 639– 673.
- Ghoubay-Benallaoua, D., Basli, E., Goldschmidt, P., Pecha, F., Chaumeil, C., Laroche, L. and Borderie, V., Human epithelial cell cultures from superficial limbal explants. Mol. Vis., 2011, 17, 341–354.
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