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  • 1.
    Mikhailova, Alexandra
    et al.
    BioMediTech, University of Tampere, Tampere, Finland.
    Ilmarinen, Tanja
    Faculty of Medicine, University of Szeged, Szeged, Hungary.
    Ratnayake, Anjula
    LinkoCare Life Sciences AB.
    Petrovski, Goran
    Faculty of Medicine, University of Szeged, Szeged, Hungary.
    Uusitalo, Hannu
    University of Tampere and Tays Eye Center, Tampere, Finland.
    Skottman, Heli
    BioMediTech, University of Tampere, Tampere, Finland.
    Rafat, Mehrdad
    Linköping University, Department of Biomedical Engineering, Biomedical Instrumentation. Linköping University, Faculty of Science & Engineering. LinkoCare Life Sciences AB.
    Human pluripotent stem cell-derived limbal epithelial stem cells on bioengineered matrices for corneal reconstruction2016In: Experimental Eye Research, ISSN 0014-4835, Vol. 146, p. 26-34Article in journal (Refereed)
    Abstract [en]

    Corneal epithelium is renewed by limbal epithelial stem cells (LESCs), a type of tissue-specific stem cells located in the limbal palisades of Vogt at the corneo-scleral junction. Acute trauma or inflammatory disorders of the ocular surface can destroy these stem cells, leading to limbal stem cell deficiency (LSCD) – a painful and vision-threatening condition. Treating these disorders is often challenging and complex, especially in bilateral cases with extensive damage. Human pluripotent stem cells (hPSCs) provide new opportunities for corneal reconstruction using cell-based therapy. Here, we investigated the use of hPSC-derived LESC-like cells on bioengineered collagen matrices in serum-free conditions, aiming for clinical applications to reconstruct the corneal epithelium and partially replace the damaged stroma. Differentiation of hPSCs towards LESC-like cells was directed using small-molecule induction followed by maturation in corneal epithelium culture medium. After four to five weeks of culture, differentiated cells were seeded onto bioengineered matrices fabricated as transparent membranes of uniform thickness, using medical-grade porcine collagen type I and a hybrid cross-linking technology. The bioengineered matrices were fully transparent, with high water content and swelling capacity, and parallel lamellar microstructure. Cell proliferation of hPSC-LESCs was significantly higher on bioengineered matrices than on collagen-coated control wells after two weeks of culture, and LESC markers p63 and cytokeratin 15, along with proliferation marker Ki67 were expressed even after 30 days in culture. Overall, hPSC-LESCs retained their capacity to self-renew and proliferate, but were also able to terminally differentiate upon stimulation, as suggested by protein expression of cytokeratins 3 and 12. We propose the use of bioengineered collagen matrices as carriers for the clinically-relevant hPSC-derived LESC-like cells, as a novel tissue engineering approach for corneal reconstruction.

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