| Literature DB >> 32807933 |
Matthew P Murphy1,2,3, Lauren S Koepke2, Michael T Lopez2, Xinming Tong4, Thomas H Ambrosi2, Gunsagar S Gulati1, Owen Marecic1, Yuting Wang2,5, Ryan C Ransom1,2, Malachia Y Hoover1, Holly Steininger2, Liming Zhao2,5, Marcin P Walkiewicz6, Natalina Quarto2, Benjamin Levi7, Derrick C Wan2, Irving L Weissman1, Stuart B Goodman4,8, Fan Yang4,8, Michael T Longaker9,10, Charles K F Chan11,12.
Abstract
Osteoarthritis (OA) is a degenerative disease resulting in irreversible, progressive destruction of articular cartilage1. The etiology of OA is complex and involves a variety of factors, including genetic predisposition, acute injury and chronic inflammation2-4. Here we investigate the ability of resident skeletal stem-cell (SSC) populations to regenerate cartilage in relation to age, a possible contributor to the development of osteoarthritis5-7. We demonstrate that aging is associated with progressive loss of SSCs and diminished chondrogenesis in the joints of both mice and humans. However, a local expansion of SSCs could still be triggered in the chondral surface of adult limb joints in mice by stimulating a regenerative response using microfracture (MF) surgery. Although MF-activated SSCs tended to form fibrous tissues, localized co-delivery of BMP2 and soluble VEGFR1 (sVEGFR1), a VEGF receptor antagonist, in a hydrogel skewed differentiation of MF-activated SSCs toward articular cartilage. These data indicate that following MF, a resident stem-cell population can be induced to generate cartilage for treatment of localized chondral disease in OA.Entities:
Mesh:
Year: 2020 PMID: 32807933 PMCID: PMC7704061 DOI: 10.1038/s41591-020-1013-2
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440