The effect of extracellular ATP-induced neutrophil on endotoxin hepatitis in mice
Project/Area Number |
23790436
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Multi-year Fund |
Research Field |
Experimental pathology
|
Research Institution | Niigata University of Health and Welfare (2013) Niigata University (2011-2012) |
Principal Investigator |
KAWAMURA Hiroki 新潟医療福祉大学, 医療技術学部, 講師 (20333495)
|
Project Period (FY) |
2011 – 2013
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
|
Keywords | マクロファージ / ATP / 好中球 / MIP-2 / KC / P2受容体 / LPS |
Research Abstract |
Extracellular ATP leads to immune responses in a wide spectrum of cell types (e.g., macrophages, T cells) and tissues. Our previous study shows that extracellular ATP-stimulated macrophages produce MIP-2. Thus, we investigated the role of ATP-mediated inflammatory response by macrophages in LPS-induced endotoxin shock model mouse. This study indicated that an increased production of reactive oxygen species by ATP-stimulated macrophages activates the signalling pathways that promote MIP-2 production which, in turn, induces neutrophil migration. Unfortunately, this pathway did not affect pathogenic mechanism in LPS-induced endotoxin shock model mouse.
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Report
(4 results)
Research Products
(11 results)