Epithelial wound healing in a model of porcine corneas stored in an innovative bioreactor

Purpose Experimental models of corneal epithelial healing are critically important to study cellular mechanisms and new therapeutics. We designed a bioreactor (BR) for exvivo corneal storage. It restores a pressure equivalent to the intraocular pressure in the endothelial chamber while allowing cont...

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Veröffentlicht in:Acta ophthalmologica (Oxford, England) England), 2015-10, Vol.93 (S255), p.n/a
Hauptverfasser: Guindolet, D., He, Z., Bernard, A., Regeade, D., Piselli, S., Perrache, C., Forest, F., Peoch, M., Gain, P., Gabison, E., Thuret, G.
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container_issue S255
container_start_page
container_title Acta ophthalmologica (Oxford, England)
container_volume 93
creator Guindolet, D.
He, Z.
Bernard, A.
Regeade, D.
Piselli, S.
Perrache, C.
Forest, F.
Peoch, M.
Gain, P.
Gabison, E.
Thuret, G.
description Purpose Experimental models of corneal epithelial healing are critically important to study cellular mechanisms and new therapeutics. We designed a bioreactor (BR) for exvivo corneal storage. It restores a pressure equivalent to the intraocular pressure in the endothelial chamber while allowing continuous renewing of media in both epithelial and endothelial chambers. It comprised 2 transparent windows for direct observation of epi and endo layers. Initially designed for human corneas, we adapted a prototype for porcine corneas to develop a new experimental platform. Aim: to study epithelial wound healing in the BR compared to a standard ex‐vivo model of porcine corneas. Methods Porcine eyeballs were obtained from a local slaughterhouse within 4 hours after death. Excised corneas were stored either in a BR or in a Petri dish with culture medium and agar for 4 weeks. A 5 mm epithelial debridmentulcer was performed. Exposition of the epithelium to various conditions was assessed in parallel: air‐lifting, immersion in different media, alternating media and air. Experiments were done in triplicate. Healing rate was monitored with fluorescein staining, digital pictures, and image analysis with ImageJ. After complete healing, corneas were processed for histology and immunolabelling with K3‐K12, laminin‐5, 5‐ethynyl‐2′‐deoxyuridine (EdU), ABCB5, and PAX6. Results Faster epithelial healing was observed for cornea stored in bioreactor. In bioreactor epithelial layer was mature (K3‐K12 immunostaining) and multi‐layered. Basement membrane was also restored (laminin‐5 immunostaining). Repeated epithelial debridement successfully healed indicating adequate survival of progenitors Conclusions This innovative porcine bioreactor could be a new ex‐vivo assay to study corneal wound healing and to assess efficacy or toxicity of new therapeutics. Grant: UJM, ANSM.
doi_str_mv 10.1111/j.1755-3768.2015.0343
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We designed a bioreactor (BR) for exvivo corneal storage. It restores a pressure equivalent to the intraocular pressure in the endothelial chamber while allowing continuous renewing of media in both epithelial and endothelial chambers. It comprised 2 transparent windows for direct observation of epi and endo layers. Initially designed for human corneas, we adapted a prototype for porcine corneas to develop a new experimental platform. Aim: to study epithelial wound healing in the BR compared to a standard ex‐vivo model of porcine corneas. Methods Porcine eyeballs were obtained from a local slaughterhouse within 4 hours after death. Excised corneas were stored either in a BR or in a Petri dish with culture medium and agar for 4 weeks. A 5 mm epithelial debridmentulcer was performed. Exposition of the epithelium to various conditions was assessed in parallel: air‐lifting, immersion in different media, alternating media and air. Experiments were done in triplicate. Healing rate was monitored with fluorescein staining, digital pictures, and image analysis with ImageJ. After complete healing, corneas were processed for histology and immunolabelling with K3‐K12, laminin‐5, 5‐ethynyl‐2′‐deoxyuridine (EdU), ABCB5, and PAX6. Results Faster epithelial healing was observed for cornea stored in bioreactor. In bioreactor epithelial layer was mature (K3‐K12 immunostaining) and multi‐layered. Basement membrane was also restored (laminin‐5 immunostaining). Repeated epithelial debridement successfully healed indicating adequate survival of progenitors Conclusions This innovative porcine bioreactor could be a new ex‐vivo assay to study corneal wound healing and to assess efficacy or toxicity of new therapeutics. 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We designed a bioreactor (BR) for exvivo corneal storage. It restores a pressure equivalent to the intraocular pressure in the endothelial chamber while allowing continuous renewing of media in both epithelial and endothelial chambers. It comprised 2 transparent windows for direct observation of epi and endo layers. Initially designed for human corneas, we adapted a prototype for porcine corneas to develop a new experimental platform. Aim: to study epithelial wound healing in the BR compared to a standard ex‐vivo model of porcine corneas. Methods Porcine eyeballs were obtained from a local slaughterhouse within 4 hours after death. Excised corneas were stored either in a BR or in a Petri dish with culture medium and agar for 4 weeks. A 5 mm epithelial debridmentulcer was performed. Exposition of the epithelium to various conditions was assessed in parallel: air‐lifting, immersion in different media, alternating media and air. Experiments were done in triplicate. Healing rate was monitored with fluorescein staining, digital pictures, and image analysis with ImageJ. After complete healing, corneas were processed for histology and immunolabelling with K3‐K12, laminin‐5, 5‐ethynyl‐2′‐deoxyuridine (EdU), ABCB5, and PAX6. Results Faster epithelial healing was observed for cornea stored in bioreactor. In bioreactor epithelial layer was mature (K3‐K12 immunostaining) and multi‐layered. Basement membrane was also restored (laminin‐5 immunostaining). Repeated epithelial debridement successfully healed indicating adequate survival of progenitors Conclusions This innovative porcine bioreactor could be a new ex‐vivo assay to study corneal wound healing and to assess efficacy or toxicity of new therapeutics. 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title Epithelial wound healing in a model of porcine corneas stored in an innovative bioreactor
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