1998 Fiscal Year Final Research Report Summary
Development of C57BL/6J-AgtKO mice
Project/Area Number |
09680826
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Laboratory animal science
|
Research Institution | University of Tsukuba |
Principal Investigator |
FUKAMIZU Akiyoshi Institute of Applied Biochemistry, University of Tsukuba, 応用生物化学系, 助教授 (60199172)
|
Co-Investigator(Kenkyū-buntansha) |
HORIGUCHI Hisashi Ibaraki Prefectural University of Health Sciences, 助手 (30238795)
YAGAMI Ken-ichi Institute of Basic Medical Sciences, University of Tsukuba, 基礎医学系, 教授 (40166476)
|
Project Period (FY) |
1997 – 1998
|
Keywords | Angiotensinogen / knockout / Renin-angiotensin system / Hydronephersis / Blood-brain barrier |
Research Abstract |
We previously developed hypotensive mice by gene-targeting technique to understand the function of angiotensinogen gene. The angiotensinogen-deficient (AgtKO) mice were maintained with mixed C57BL/6J, CBA, and ICR hybrid genetic background. Therefore development of AgtKO mice with homogeneous genetic background is needed. 1) We developed AgtKO with genetic background of C57BL/6J (C57BL/6J-AgtKO) by speedy backcrossing through in virtro fertilization, using pre-pubertal superovulation. 2) We demonstrated that C57BL/6J-AgtKO mice die before weaning. 3) We indicated that mortality in C57BL/6J-AgtKO can be reduced by hypodermic saline injection in the 7 days following birth and that C57BL/6J-AgtKO are developed hydronephrosis by day 14. 4) The apoptotic induction is involved in the development of hydronephrosis on C57BL/6J-AgtKO. 5) We also demonstrated that the hydronephrosis is prevented by genetic rescue of the angiotensinogen gene. 6) Furthermore we indicated that the Agt gene are required for functional maintenance of blood-brain barrier.
|