Abstract

ObjectiveHyaluronic acid–transglutaminase (HA-TG) is an enzymatically crosslinkable adhesive hydrogel with chondrogenic properties demonstrated in vitro and in an ectopic mouse model. In this study, we investigated the feasibility of using HA-TG in a collagen scaffold to treat chondral lesions in an ovine model, to evaluate cartilage regeneration in a mechanically and biologically challenging joint environment, and the influence of the surgical procedure on the repair process.DesignChondral defects of 6-mm diameter were created in the stifle joint of skeletally mature sheep. In a 3-month study, 6 defects were treated with HA-TG in a collagen scaffold to test the stability and biocompatibility of the defect filling. In a 6-month study, 6 sheep had 12 defects treated with HA-TG and collagen and 2 sheep had 4 untreated defects. Histologically observed quality of repair tissue and adjacent cartilage was semiquantitatively assessed.ResultsHA-TG adhered to the native tissue and did not cause any detectable negative reaction in the surrounding tissue. HA-TG in a collagen scaffold supported infiltration and chondrogenic differentiation of mesenchymal cells, which migrated from the subchondral bone through the calcified cartilage layer. Additionally, HA-TG and collagen treatment led to better adjacent cartilage preservation compared with empty defects (P < 0.05).ConclusionsThis study demonstrates that the adhesive HA-TG hydrogel in a collagen scaffold shows good biocompatibility, supports in situ cartilage regeneration and preserves the surrounding cartilage. This proof-of-concept study shows the potential of this approach, which should be further considered in the treatment of cartilage lesions using a single-step procedure.

Highlights

  • Articular cartilage has a limited ability to self-repair after injuries

  • The limited capability of cartilage to heal has driven the development of tissue engineering strategies such as microfracture, autologous chondrocyte implantation (ACI), and matrix-assisted autologous chondrocyte implantation (MACI).[4,5]

  • When repair tissue was present in the cartilage defect, the structural cell organization resembled the one in native articular cartilage, with elongated cells in the superficial layer and more round cells in the deeper zones (Fig. 2D)

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Summary

Introduction

Articular cartilage has a limited ability to self-repair after injuries. This is partly due to its avascular nature that prevents progenitor cells in blood to migrate to the site of the lesion and the limited number of resident cells.[1]. Cell-free approaches, using smart biomaterials able to recruit chondrogenic cells and support their differentiation, hold great promises for the development

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