Intracorneal Implantation of 3D Bioprinted Scaffolds Containing Mesenchymal Stromal Cells Using Femtosecond‐Laser‐Assisted Intrastromal Keratoplasty

Author:

Boix‐Lemonche Gerard1ORCID,Nagymihaly Richard M.2,Niemi Essi M.34,Josifovska Natasha1ORCID,Johansen Stian5,Moe Morten C.12,Scholz Hanne46ORCID,Petrovski Goran127ORCID

Affiliation:

1. Center for Eye Research and Innovative Diagnostics Department of Ophthalmology Institute of Clinical Medicine Faculty of Medicine University of Oslo Oslo 0450 Norway

2. Department of Ophthalmology Oslo University Hospital Oslo 0450 Norway

3. Vascular Biology and Surgery Group Institute for Surgical Research and Department of Vascular Surgery Oslo University Hospital Post Box 4950 Oslo Nydalen N‐0424 Norway

4. Hybrid Technology Hub Centre of Excellence Institute of Basic Medical Sciences University of Oslo Oslo 0349 Norway

5. Alcon Nordic A/S Oslo Lisaker 1366 Norway

6. Cell Transplantation and Tissue Engineering Group Institute for Surgical Research and Section for Transplant Surgery Oslo University Hospital Post Box 4950 Oslo Nydalen N‐0424 Norway

7. Department of Ophthalmology University of Split School of Medicine and University Hospital Centre Split Croatia

Abstract

AbstractInjury of the cornea is a complex biological process. Regeneration of the corneal stroma can be facilitated by the presence of mesenchymal stromal cells (MSCs) and application of tissue equivalents. A new tissue‐engineering strategy for corneal stroma regeneration is presented using cellularized 3D bioprinted hydrogel constructs implanted into organ cultured porcine corneas using femtosecond laser‐assisted intrastromal keratoplasty. The ex vivo cultured, MSC‐loaded 3D bioprinted structures remain intact, support cell survival, and contain de novo synthesized extracellular matrix components and migrating cells throughout the observation period. At day 14 postimplantation, the cellularized tissue equivalents contain few or no cells, as demonstrated by optical coherence tomography imaging and immunofluorescent staining. This study successfully combines a laboratory‐based method with modern, patient‐care practice to produce a cell‐laden tissue equivalent for corneal implantation. Optimal bioink composition and cellularization of tissue equivalents are essential in fine‐tuning a method to promote the current technique as a future treatment modality.

Funder

H2020 Marie Skłodowska-Curie Actions

Norges Forskningsråd

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Biomaterials,Bioengineering,Biotechnology

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