DJ-1 promotes angiogenesis and osteogenesis by activating FGF receptor-1 signaling

Authors
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
Issue Date
2012-12
Publisher
NATURE PUBLISHING GROUP
Citation
NATURE COMMUNICATIONS, v.3
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.
Keywords
ENDOTHELIAL-GROWTH-FACTOR; BONE-FORMATION; PARKINSONS-DISEASE; PROTEIN-KINASE; CELLS; VEGF; EXPRESSION; PATHWAY; DEFECT; IDENTIFICATION; ENDOTHELIAL-GROWTH-FACTOR; BONE-FORMATION; PARKINSONS-DISEASE; PROTEIN-KINASE; CELLS; VEGF; EXPRESSION; PATHWAY; DEFECT; IDENTIFICATION; Signaling
ISSN
2041-1723
URI
https://pubs.kist.re.kr/handle/201004/128586
DOI
10.1038/ncomms2313
Appears in Collections:
KIST Article > 2012
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