Adipose Micro-Grafts Enhance Tendinopathy Healing in Ovine Model: An in Vivo Experimental Perspective Study

Author:

Palumbo Piccionello Angela1ORCID,Riccio Valentina1,Senesi Letizia2,Volta Antonella3,Pennasilico Luca1,Botto Riccardo1,Rossi Giacomo1,Tambella Adolfo Maria1ORCID,Galosi Livio1ORCID,Marini Carlotta1,Vullo Cecilia1,Gigante Antonio4ORCID,Zavan Barbara5ORCID,De Francesco Francesco2ORCID,Riccio Michele2ORCID

Affiliation:

1. School of Biosciences and Veterinary Medicine, University of Camerino, Matelica, Italy

2. Department of Plastic and Reconstructive Surgery-Hand Surgery Unit  Azienda ‘OspedaliRiuniti’ Ancona, Ancona, Italy

3. Department of Veterinary Medicine Science  University of Parma, Parma, Italy

4. Clinical Orthopaedics, Department of Clinical and Molecular Science  Polytechnic University of Marche, Ancona, Italy

5. Department of Morphology, Surgery and Experimental Medicine  University of Ferrara, Ferrara, Italy

Abstract

Abstract In Europe, approximatively 100 000 to 500 000 tendon repairs are performed every year. These procedures are associated with a considerable rate of postoperative complications (from 6% to 11%). Autologous micro-grafts (AAMG) and stromal vascular fraction (SVF) have been shown to improve tendon healing in 60% to 70% of treated rodents. The purpose of this study was to evaluate the effects of AAMG in a sheep model with tendinopathy. We used sheep models because, as a large animal, they are more comparable to humans. The hypothesis was that SVF injection would improve tendon healing compared with the control group, reducing inflammatory and matrix degrading, while increasing anti-inflammatory expression and collagen synthesis in the early stage of tendon injury. Sixteen Apennine sheep aged 2 to 5 years underwent 500 UI type I collagenase injection into both common calcaneal tendons (CCT) to induce tendinopathy. After 15 days (T0), one CCT in every ovine underwent randomly to 2.5 mL of AAMG obtained by mechanical disruption and the contralateral CCTs received no treatment. Clinical, ecographic, and sonographic evaluations were performed after 4 weeks (T1) and 8 weeks (T2). Histological, immunohistochemical, real-time polymerase chain reaction (RT-PCR), and biomechanical evaluations were performed at T2. At T2, the treated group showed a final tendon diameter (9.1 ± 1.4 mm) and a hardness expression (62%) that were similar to the original healthy tendon (8.1 ± 1.1 mm; 100%), with a significant recovery compared with the control group (9.5 ± 1.7 mm; 39%). Moreover, histological analysis of the treated group revealed an improvement in the fiber orientation score, fiber edema score, infiltrative-inflammatory process, and necrosis score (4.3 ± 3.3) compared with control group (8.8 ± 2.9). Immunohistochemically, the treated group showed high expression of collagen 1, Factor VIII and significantly low expression of collagen 3. These data were confirmed by RT-PCR analysis. The study findings suggested that AAMGs obtained through mechanical disruption present a safe, efficient, and reliable technique, enhancing tendon healing.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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