2014 Fiscal Year Final Research Report
Elucidation of pathological condition of sepsis by using iPS cells for creation of novel therapy
Project/Area Number |
25861727
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Multi-year Fund |
Research Field |
Emergency medicine
|
Research Institution | Nara Medical University |
Principal Investigator |
KASUDA Shogo 奈良県立医科大学, 医学部, 助教 (70434941)
|
Project Period (FY) |
2013-04-01 – 2015-03-31
|
Keywords | 敗血症 / sphingosine-1-phosphate / 血管内皮細胞 |
Outline of Final Research Achievements |
iPS cells differentiated into hematopoietic embryoid body (EB) in order to establish novel therapy for sepsis. We revealed that EB protected the endothelial integrity by producing Sphingosine-1-phosphate (S1P). Intravenous injection of EB into sepsis mice significantly restored their survival rates compared to saline-injected mice. Also, onset of lung edema was protected by EB injection. S1P produced from EB exerted protective effects on endothelial integrity of lungs, resulting in inhibition of sepsis progression.
|
Free Research Field |
血管生物学 血液凝固学
|