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Use of recombinant human stromal cell-derived factor 1α-loaded fibrin/hyaluronic acid hydrogel networks to achieve functional repair of full-thickness bovine articular cartilage via homing of chondrogenic progenitor cells
Journal article   Open access

Use of recombinant human stromal cell-derived factor 1α-loaded fibrin/hyaluronic acid hydrogel networks to achieve functional repair of full-thickness bovine articular cartilage via homing of chondrogenic progenitor cells

Yin Yu, Marc J Brouillette, Dongrim Seol, Hongjun Zheng, Joseph A Buckwalter and James A Martin
Arthritis & rheumatology (Hoboken, N.J.), Vol.67(5), pp.1274-1285
05/2015
DOI: 10.1002/art.39049
PMID: 25623441
url
https://www.ncbi.nlm.nih.gov/pmc/articles/11752793View
Open Access

Abstract

Articular cartilage damage after joint trauma seldom heals and often leads to osteoarthritis. We previously identified a migratory chondrogenic progenitor cell (CPC) population that responds chemotactically to cell death and rapidly repopulates the injured cartilage matrix, which suggests a potential approach for articular cartilage repair. This study was undertaken to determine whether recombinant human stromal cell-derived factor 1α (rhSDF-1α), a potent CPC chemoattractant, would improve the quality of cartilage regeneration, hypothesizing that increased recruitment of CPCs by rhSDF-1α would promote the formation of cartilage matrix upon chondrogenic induction. Full-thickness bovine chondral defects were filled with hydrogel, composed 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 the regenerated cartilage. Use of rhSDF-1α dramatically improved CPC recruitment to the chondral defects at 12 days. After 6 weeks under chondrogenic conditions, cell morphology, proteoglycan density, and the ultrastructure of the repair tissue were all similar to that found in native cartilage. Compared with empty controls, neocartilage generated in rhSDF-1α-containing defects showed significantly greater interfacial strength, and acquired mechanical properties comparable to those of native cartilage. This study showed that stimulating local CPC recruitment prior to treatment with chondrogenic factors significantly improves the biochemical and mechanical properties of the cartilage tissue 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, which can be achieved using smart drug-delivery systems.
Cell Differentiation Hydrogel, Polyethylene Glycol Dimethacrylate - therapeutic use Recombinant Proteins - therapeutic use Hyaluronic Acid - therapeutic use Chondrocytes - cytology Humans Cells, Cultured Stem Cells - cytology Cartilage, Articular - pathology Animals Cattle Guided Tissue Regeneration - methods Cartilage, Articular - injuries Chemokine CXCL12 - therapeutic use Chondrogenesis Fibrin - therapeutic use Cell Movement

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