| Literature DB >> 32878982 |
Suzanne E Eldridge1, Aida Barawi2, Hui Wang3, Anke J Roelofs3, Magdalena Kaneva2, Zeyu Guan2, Helen Lydon4, Bethan L Thomas5, Anne-Sophie Thorup2, Beatriz F Fernandez2, Sara Caxaria2, Danielle Strachan2, Ahmed Ali2, Kanatheepan Shanmuganathan2, Costantino Pitzalis2, James R Whiteford6, Frances Henson7, Andrew W McCaskie4, Cosimo De Bari3, Francesco Dell'Accio1.
Abstract
Cartilage loss leads to osteoarthritis, the most common cause of disability for which there is no cure. Cartilage regeneration, therefore, is a priority in medicine. We report that agrin is a potent chondrogenic factor and that a single intraarticular administration of agrin induced long-lasting regeneration of critical-size osteochondral defects in mice, with restoration of tissue architecture and bone-cartilage interface. Agrin attracted joint resident progenitor cells to the site of injury and, through simultaneous activation of CREB and suppression of canonical WNT signaling downstream of β-catenin, induced expression of the chondrogenic stem cell marker GDF5 and differentiation into stable articular chondrocytes, forming stable articular cartilage. In sheep, an agrin-containing collagen gel resulted in long-lasting regeneration of bone and cartilage, which promoted increased ambulatory activity. Our findings support the therapeutic use of agrin for joint surface regeneration.Entities:
Year: 2020 PMID: 32878982 DOI: 10.1126/scitranslmed.aax9086
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956