Objective: Articular cartilage damage after joint trauma seldom heals and often leads to osteoarthritis (OA). We previously identified a migratory chondrogenic progenitor cell (CPC) population that responded chemotactically to cell death and rapidly repopulated the injured cartilage matrix, which suggested their potential for articular cartilage repair. To test that potential we determined whether SDF-1α, a potent CPC chemoattractant, would improve the quality of cartilage regeneration. We hypothesized that increased recruitment of CPCs by rhSDF-1α would promote the formation of cartilage matrix upon chondrogenic induction. Methods: Full-thickness bovine chondral defects were filled with hydrogel comprised of fibrin and hyaluronic acid and containing rhSDF-1α. Cell migration was monitored, followed by chondrogenic induction. Regenerated tissue was evaluated by histology, immunohistochemistry, and scanning electron microscopy. Push-out tests and unconfined compression tests were performed to assess the strength of tissue integration and the mechanical properties of regenerated cartilage. Results: rhSDF-1α dramatically improved CPCs recruitment to defects at 12 days. After 6 weeks under chondrogenic conditions, cell morphology, proteoglycan density, and ultrastructure of repair tissue, were similar to native cartilage. Neocartilage generated in rhSDF-1α-containing defects showed significantly greater interfacial strength than controls, and acquired mechanical properties comparable to native cartilage. Conclusion: This study showed that stimulating local CPCs recruitment prior to treatment with chondrogenic factors significantly improves the biochemical and mechanical properties of tissues formed in chondral defects. This simple approach may be implemented in vivo as a one-step procedure by staging the release of chemokine and chondrogenic factors from within the hydrogel using smart drug delivery systems. This article is protected by copyright. All rights reserved.