2010 Fiscal Year Final Research Report
Targeting cryopyrin as a new therapeutic approach to control inflammation
Project/Area Number |
20591197
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
膠原病・アレルギー・感染症内科学
|
Research Institution | Department of Clinical Research, National Hospital Organization Nagasaki Medical Center |
Principal Investigator |
MIGITA Kiyoshi Department of Clinical Research, National Hospital Organization Nagasaki Medical Center, 臨床研究センター, 病因解析研究部長 (60264214)
|
Co-Investigator(Kenkyū-buntansha) |
ISHIBASHI Hiromi 独立行政法人国立病院機構長崎医療センター, 臨床研究センター, センター長 (80127969)
EGUCHI Katumi 長崎大学, 医歯薬学総合研究科, 教授 (30128160)
|
Project Period (FY) |
2008 – 2010
|
Keywords | ryopyrin / 自己炎症性疾患 / 家族性地中海熱 / 関節リウマチ / 血清アミロイドA蛋白 |
Research Abstract |
The mechanism by which inflammasome activation and following IL-1β induction in autoinflammation is not completely elucidated. We studied the role of serum amyloid A (SAA) in the regulation of IL-1β production and activation of inflammasome cascade in human rheumatoid synoviocytes. Rheumatoid synoviocytes stimulated with SAA express NLRP3 (cryopyrin) mRAN expression. MSU (modosodium urate), a ligand for NLRP3, stimulation did not induce IL-1β production in rheumatoid synoviocytes. Whereas, rheumatoid synoviocytes pretreated with low concentration (1-5μg/ml) of SAA produce IL-1β in response to MSU. These findings indicate that during systemic inflammation, SAA may promote the MSU-induced IL-1β induction through activating the NLRP3 inflammasome activation.
|
Research Products
(5 results)
-
-
-
-
[Journal Article] MEFV mutations in Japanese rheumatoid arthritis patients.2008
Author(s)
Migita K, Nakamura T, Maeda Y, Miyashita T, Koga T, Tanaka M, Nakamura M, Komori A, Ishibashi H, Origuchi T, Ida H, Kawasaki E, Yasunami M, Eguchi K.
-
Journal Title
Clin Exp Rheumatol. 26(6)
Pages: 1091-4
Peer Reviewed
-
[Remarks] ホームページ等