Effects of Mesenchymal Stem Cell and Growth Factor Delivery on Cartilage Repair in a Mini-Pig Model

Author:

Fisher Matthew B.1234,Belkin Nicole S.12,Milby Andrew H.12,Henning Elizabeth A.12,Söegaard Nicole12,Kim Minwook12,Pfeifer Christian125,Saxena Vishal12,Dodge George R.12,Burdick Jason A.26,Schaer Thomas P.7,Steinberg David R.12,Mauck Robert L.126

Affiliation:

1. McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

2. Translational Musculoskeletal Research Center, Philadelphia VA Medical Center, Philadelphia, PA, USA

3. Department of Biomedical Engineering, University of North Carolina, Chapel Hill, NC, USA

4. North Carolina State University, Raleigh, NC, USA

5. Department of Trauma Surgery, Regensburg University Medical Center, Regensburg, Germany

6. Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA

7. Comparative Orthopaedic Research Laboratory, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Objective We have recently shown that mesenchymal stem cells (MSCs) embedded in a hyaluronic acid (HA) hydrogel and exposed to chondrogenic factors (transforming growth factor–β3 [TGF-β3]) produce a cartilage-like tissue in vitro. The current objective was to determine if these same factors could be combined immediately prior to implantation to induce a superior healing response in vivo relative to the hydrogel alone. Design Trochlear chondral defects were created in Yucatan mini-pigs (6 months old). Treatment groups included an HA hydrogel alone and hydrogels containing allogeneic MSCs, TGF-β3, or both. Six weeks after surgery, micro-computed tomography was used to quantitatively assess defect fill and subchondral bone remodeling. The quality of cartilage repair was assessed using the ICRS-II histological scoring system and immunohistochemistry for type II collagen. Results Treatment with TGF-β3 led to a marked increase in positive staining for collagen type II within defects ( P < 0.05), while delivery of MSCs did not ( P > 0.05). Neither condition had an impact on other histological semiquantitative scores ( P > 0.05), and inclusion of MSCs led to significantly less defect fill ( P < 0.05). For all measurements, no synergistic interaction was found between TGF-β3 and MSC treatment when they were delivered together ( P > 0.05). Conclusions At this early healing time point, treatment with TGF-β3 promoted the formation of collagen type II within the defect, while allogeneic MSCs had little benefit. Combination of TGF-β3 and MSCs at the time of surgery did not produce a synergistic effect. An in vitro precultured construct made of these components may be required to enhance in vivo repair in this model system.

Publisher

SAGE Publications

Subject

Physical Therapy, Sports Therapy and Rehabilitation,Biomedical Engineering,Immunology and Allergy

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