Human Multipotent Mesenchymal Stromal Cells in the Treatment of Postoperative Temporal Bone Defect: An Animal Model

Author:

Skoloudik Lukas1,Chrobok Viktor1,Kalfert David1,Koci Zuzana234,Sykova Eva23,Chumak Tetyana2,Popelar Jiri2,Syka Josef2,Laco Jan5,Dedková Jana6,Dayanithi Govindan2789,Filip Stanislav10

Affiliation:

1. Department of Otorhinolaryngology and Head and Neck Surgery, University Hospital Hradec Kralové, Charles University in Prague, Faculty of Medicine in Hradec Kralové, Hradec Kralové, Czech Republic

2. Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic

3. Department of Neuroscience, 2nd Faculty of Medicine, Charles University in Prague, Prague, Czech Republic

4. Bioinova, Ltd., Prague, Czech Republic

5. The Fingerland Department of Pathology, University Hospital Hradec Kralové, Charles University in Prague, Faculty of Medicine in Hradec Kralové, Hradec Kralové, Czech Republic

6. Department of Radiology, University Hospital Hradec Kralové, Charles University in Prague, Faculty of Medicine in Hradec Kralové, Hradec Kralové, Czech Republic

7. Department of Molecular Neurophysiology, Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic

8. Institut National de la Santé et de la Recherche Médicale, Unité de recherche U1198, Université Montpellier, Montpellier, France

9. Ecole Pratique des Hautes Etudes-Sorbonne, Paris, France

10. Department of Oncology and Radiotherapy, Charles University in Prague, Faculty of Medicine in Hradec Kralové, Hradec Kralové, Czech Republic

Abstract

Canal wall down mastoidectomy is one of the most effective treatments for cholesteatoma. However, it results in anatomical changes in the external and middle ear with a negative impact on the patient's quality of life. To provide complete closure of the mastoid cavity and normalize the anatomy of the middle and external ear, we used human multipotent mesenchymal stromal cells (hMSCs), GMP grade, in a guinea pig model. A method for preparing a biomaterial composed of hMSCs, hydroxyapatite, and tissue glue was developed. Animals from the treated group were implanted with biomaterial composed of hydroxyapatite and hMSCs, while animals in the control group received hydroxyapatite alone. When compared to controls, the group implanted with hMSCs showed a significantly higher ratio of new bone formation ( p = 0.00174), as well as a significantly higher volume percentage of new immature bone ( p = 0.00166). Our results proved a beneficial effect of hMSCs on temporal bone formation and provided a promising tool to improve the quality of life of patients after canal wall down mastoidectomy by hMSC implantation.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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