2010 Fiscal Year Final Research Report
Clarification of the function of TIMP3 in fracture healing and development of new fracture healing drug
Project/Area Number |
21792077
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Orthodontic/Pediatric dentistry
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Research Institution | The University of Tokushima |
Principal Investigator |
HIASA Masahiro The University of Tokushima, 大学院・ヘルスバイオサイエンス研究部, 助教 (90511337)
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Project Period (FY) |
2009 – 2010
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Keywords | 破骨細胞 / 樹状細胞 / 骨折治癒 |
Research Abstract |
Monocytes can give rise to osteoclasts (OCs), and dendritic cells (DCs), but these differentiation mechanism is unclear. We clarified that BMSCs up-modulate M-CSF receptor on monocytes through TIMP-3 elaborated by BMSCs to facilitate osteoclastogenesis and suppress DC differentiation, and that TIMP-3 expression is induced in OCs by themselves during osteoclastogenesis to further block TACE activity and enhance the surface expression of M-CSF receptor. This study demonstrated that the suppression of TACE-mediated shedding of M-CSF receptor by BMSCs may dysregulate monocyte differentiation towards OCs to cause bone resorption and anti-inflammatory response in bone remodeling.
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Research Products
(7 results)
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[Journal Article] GM-CSF and IL-4 induce dendritic cell differentiation and disrupt osteoclastogenesis through M-CSF receptor shedding by up-regulation of TNF-alpha converting enzyme (TACE).2009
Author(s)
Hiasa M, Abe M, Nakano A, Oda A, AmouH, Kido S, Takeuchi K, Kagawa K, YataK, Hashimoto T, Ozaki S, Asaoka K,Tanaka E, Moriyama K, Matsumoto T.
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Journal Title
Blood. 114(20)
Pages: 4517-4526
Peer Reviewed
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[Remarks] ホームページ等