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Suh, Pann-Ghill
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DJ-1 promotes angiogenesis and osteogenesis by activating FGF receptor-1 signaling

Author(s)
Kim, Jung-MinShin, Hong-InCha, Sun-ShinLee, Chang SupHong, Bok SilLim, SeyoungJang, Hyun-JunKim, JaeyoonYang, Yong RyoulKim, Yun-HeeYun, SangukRijal, GirdhariLee-Kwon, WhaseonSeo, Jeong KonGho, Yong SongRyu, Sung HoHur, Eun-MiSuh, Pann-Ghill
Issued Date
2012-12
DOI
10.1038/ncomms2313
URI
https://scholarworks.unist.ac.kr/handle/201301/3402
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84871775091
Citation
NATURE COMMUNICATIONS, v.3, pp.1 - 11
Abstract
Communication between osteoblasts and endothelial cells is essential for bone fracture repair, but the molecular identities of such communicating factors are not well defined. Here we identify DJ-1 as a novel mediator of the cross-talk between osteoblasts and endothelial cells through an unbiased screening of molecules secreted from human mesenchymal stem cells during osteogenesis. We show that DJ-1 stimulates the differentiation of human mesenchymal stem cells to osteoblasts and that DJ-1 induces angiogenesis in endothelial cells through activation of fibroblast growth factor receptor-1 signalling. In a rodent model of bone fracture repair, extracellular application of DJ-1 enhances bone regeneration in vivo by stimulating the formation of blood vessels and new bones. Both these effects are blocked by antagonizing fibroblast growth factor receptor-1 signalling. These findings uncover previously undefined extracellular roles of DJ-1 to promote angiogenesis and osteogenesis, suggesting DJ-1 may have therapeutic potential to stimulate bone regeneration.
Publisher
NATURE PUBLISHING GROUP
ISSN
2041-1723
Keyword
ENDOTHELIAL-GROWTH-FACTORBONE MORPHOGENETIC PROTEIN-4PARKINSONS-DISEASEOXIDATIVE STRESSDEFECT MODELCELLSVEGFREGENERATIONEXPRESSIONPATHWAYS

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