Honeycomb porous films as permeable scaffold materials for human embryonic stem cell-derived retinal pigment epithelium
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Honeycomb porous films as permeable scaffold materials for human embryonic stem cell-derived retinal pigment epithelium. / Calejo, Maria Teresa; Ilmarinen, Tanja; Jongprasitkul, Hatai; Skottman, Heli; Kellomäki, Minna.
In: Journal of Biomedical Materials Research. Part A, Vol. 104, No. 7, 01.07.2016, p. 1646-1656.Research output: Contribution to journal › Article › Scientific › peer-review
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TY - JOUR
T1 - Honeycomb porous films as permeable scaffold materials for human embryonic stem cell-derived retinal pigment epithelium
AU - Calejo, Maria Teresa
AU - Ilmarinen, Tanja
AU - Jongprasitkul, Hatai
AU - Skottman, Heli
AU - Kellomäki, Minna
PY - 2016/7/1
Y1 - 2016/7/1
N2 - Age-related macular degeneration (AMD) is a leading cause of blindness in developed countries, characterised by the degeneration of the retinal pigment epithelium (RPE), a pigmented cell monolayer that closely interacts with the photoreceptors. RPE transplantation is thus considered a very promising therapeutic option to treat this disease. In this work, porous honeycomb-like films are for the first time investigated as scaffold materials for human embryonic stem cell-derived retinal pigment epithelium (hESC-RPE). By changing the conditions during film preparation, it was possible to produce films with homogeneous pore distribution and adequate pore size (3-5 μm), that is large enough to ensure high permeability but small enough to enable cell adherence and spreading. A brief dip-coating procedure with collagen type IV enabled the homogeneous adsorption of the protein to the walls and bottom of pores, increasing the hydrophilicity of the surface. hESC-RPE adhered and proliferated on all the collagen-coated materials, regardless of small differences in pore size. The differentiation of hESC-RPE was confirmed by the detection of specific RPE protein markers. These results suggest that the porous honeycomb films can be promising candidates for hESC-RPE tissue engineering, importantly enabling the free flow of ions and molecules across the material.
AB - Age-related macular degeneration (AMD) is a leading cause of blindness in developed countries, characterised by the degeneration of the retinal pigment epithelium (RPE), a pigmented cell monolayer that closely interacts with the photoreceptors. RPE transplantation is thus considered a very promising therapeutic option to treat this disease. In this work, porous honeycomb-like films are for the first time investigated as scaffold materials for human embryonic stem cell-derived retinal pigment epithelium (hESC-RPE). By changing the conditions during film preparation, it was possible to produce films with homogeneous pore distribution and adequate pore size (3-5 μm), that is large enough to ensure high permeability but small enough to enable cell adherence and spreading. A brief dip-coating procedure with collagen type IV enabled the homogeneous adsorption of the protein to the walls and bottom of pores, increasing the hydrophilicity of the surface. hESC-RPE adhered and proliferated on all the collagen-coated materials, regardless of small differences in pore size. The differentiation of hESC-RPE was confirmed by the detection of specific RPE protein markers. These results suggest that the porous honeycomb films can be promising candidates for hESC-RPE tissue engineering, importantly enabling the free flow of ions and molecules across the material.
KW - honeycomb films
KW - permeability
KW - pluripotent stem cells
KW - retinal pigment epithelium
KW - tissue engineering
U2 - 10.1002/jbm.a.35690
DO - 10.1002/jbm.a.35690
M3 - Article
VL - 104
SP - 1646
EP - 1656
JO - Journal of Biomedical Materials Research. Part A
JF - Journal of Biomedical Materials Research. Part A
SN - 1549-3296
IS - 7
ER -