软骨
骨关节炎
再生(生物学)
干细胞
医学
细胞生物学
关节软骨
病理
解剖
生物
替代医学
作者
Matthew P. Murphy,Lauren S. Koepke,Michael T. Lopez,Xinming Tong,Thomas H. Ambrosi,Gunsagar S. Gulati,Owen Marecic,Yuting Wang,Ryan C. Ransom,Malachia Hoover,Holly Steininger,Liming Zhao,Marcin P. Walkiewicz,Natalina Quarto,Benjamin Lévi,Derrick C. Wan,Irving L. Weissman,Stuart B. Goodman,Fan Yang,Michael T. Longaker,Charles K. F. Chan
出处
期刊:Nature Medicine
[Springer Nature]
日期:2020-08-17
卷期号:26 (10): 1583-1592
被引量:228
标识
DOI:10.1038/s41591-020-1013-2
摘要
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.
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