Project/Area Number |
10212202
|
Research Category |
Grant-in-Aid for Scientific Research on Priority Areas (B)
|
Allocation Type | Single-year Grants |
Review Section |
Biological Sciences
|
Research Institution | Teikyo University (2000-2001) The University of Tokyo (1998-1999) |
Principal Investigator |
INOUE Keizo TEIKYO UNIVERSITY, PHARMACEUTICAL SCIENCES, PROFESSOR, 薬学部, 教授 (30072937)
|
Co-Investigator(Kenkyū-buntansha) |
AOKI Junken THE TOKYO UNIVERSITY, PHARMACEUTICAL SCIENCES, ASSISTANT PROFESSOR, 大学院・薬学系研究科, 助教授 (20250219)
ARAI Hiroyuki THE TOKYO UNIVERSITY, PHARMACEUTICAL SCIENCES, PROFESSOR, 大学院・薬学系研究科, 教授 (40167987)
|
Project Period (FY) |
1998 – 2001
|
Project Status |
Completed (Fiscal Year 2001)
|
Budget Amount *help |
¥97,800,000 (Direct Cost: ¥97,800,000)
Fiscal Year 2001: ¥24,300,000 (Direct Cost: ¥24,300,000)
Fiscal Year 2000: ¥24,300,000 (Direct Cost: ¥24,300,000)
Fiscal Year 1999: ¥24,200,000 (Direct Cost: ¥24,200,000)
Fiscal Year 1998: ¥25,000,000 (Direct Cost: ¥25,000,000)
|
Keywords | platelet-activating factor / PHOSPHOLIPASE A / PHOSPHOLIPASE A1 / PHOSPHOLIPASE A2 / C.elegans / KNOCKOUT MICE / ホスホリパーゼA_1 / ホスホリパーゼA_2 / ノックアウトマウス / リゾホスファチジン酸 / EDG7 / ホスホリパーゼD / ホスファチジン酸 / PAF / PAF-AH / 酸化リン脂質 / リゾホスファチジルセリン |
Research Abstract |
Physiological roles of three novel phospholipases have been analysed by producing knockout animals. The phospholipases are type I platelet-activating factor acetylhydrolase (PAF-AH (I)), type II platelet-activating factor acetylhydrolase (PAF-AH (II)), and phosphatidylserine-specific phospholipase A1 (PS-PLA1). For PAF-AH (I) and PS-PLA1, we have made knock out mice, and for PAF-AH (II), we have made knockout C.elegans, as the organism express mammalian homologue of PAF-AH (II). The phenotype of each animal are shown in table ; Table : Phenotype of knockout animals animals phenotype PAF-AH (I) mice abnormality on sperm formation PAF-AH (II) c.elegans abnormality in epidermis formation PS-PLA1 mice abnormality in T cell development As these phenotype are not expected, novel function for each phospholipase is suggested, which should be solved in further studies.
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