A study of the innovative treatment for rheumatoid arthritis by regulating synoviocytes
Project/Area Number |
24592261
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Orthopaedic surgery
|
Research Institution | Kobe University |
Principal Investigator |
Miura Yasushi 神戸大学, 保健学研究科, 准教授 (60346244)
|
Research Collaborator |
FUKUDA Koji
MAEDA Toshihisa
|
Project Period (FY) |
2012-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
|
Keywords | 関節リウマチ / 滑膜線維芽細胞 / 滑膜 / インターロイキン12B |
Outline of Final Research Achievements |
The purpose of this study is to reveal the function of the signaling pathway with decoy receptor 3 (DR3) and its specific ligand TL1A on the synovitis of rheumatoid arthritis (RA) in order to establish a new therapy for RA. We newly found that the set of genes of which expression regulated by DcR3 on RA synovial fibroblasts by using microarray gene analysis. Further, we found that the expression of TPH1 and IL-12B(p40) was regulated by DcR3 and contributed to the pathogenesis of RA. We revealed that DcR3-TL1A signaling on RA synovial fibroblasts is a possible new treatment target of RA.
|
Report
(5 results)
Research Products
(29 results)