| Literature DB >> 25931016 |
Aurélien Tidu1, Djida Ghoubay-Benallaoua2, Barbara Lynch3, Bernard Haye1, Corinne Illoul1, Jean-Marc Allain3, Vincent M Borderie2, Gervaise Mosser4.
Abstract
Several diseases can lead to opacification of cornea requiring transplantation of donor tissue to restore vision. In this context, transparent collagen I fibrillated matrices have been synthesized at 15, 30, 60 and 90 mg/mL. The matrices were evaluated for fibril organizations, transparency, mechanical properties and ability to support corneal epithelial cell culture. The best results were obtained with 90 mg/mL scaffolds. At this concentration, the fibril organization presented some similarities to that found in corneal stroma. Matrices had a mean Young's modulus of 570 kPa and acellular scaffolds had a transparency of 87% in the 380-780 nm wavelength range. Human corneal epithelial cells successfully colonized the surface of the scaffolds and generated an epithelium with characteristics of corneal epithelial cells (i.e. expression of cytokeratin 3 and presence of desmosomes) and maintenance of stemness during culture (i.e. expression of ΔNp63α and formation of holoclones in colony formation assay). Presence of cultured epithelium on the matrices was associated with increased transparency (89%).Entities:
Keywords: Collagen; Human corneal epithelium; Limbal stem cell; Liquid-crystal; Transparent matrices
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Year: 2015 PMID: 25931016 DOI: 10.1016/j.actbio.2015.04.018
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947