This research will be performed primarily in Buenos Aires, Argentina at The Institute of Experimental Medicine and Biology in collaboration with Dr. Marta Tesone as an extension of the P.l's NIH parent grant # RO1 HD20869-17. The goal of this project is to elucidate the REGULATION and ROLE OF APOPTOSIS IN LUTEAL REGRESSION during the ovarian cycle and pregnancy. Preliminary experiments have determined the dynamics of pro-apoptotic gene (e.g., caspases) expression and activation in the macaque corpus luteum (CL), pursuant to their regulation and role in controlling the functional lifespan of the CL. In the present project it is proposed to pursue further this novel research on apoptosis in the corpus luteum using a more general laboratory animal model, the rat. Accordingly, the specific aims of this project are: 1) To determine the changes in the pro-apoptotic genes (caspases -2, -3, -8 and -9) during the lifespan of rat corpus luteum in the estrous cycle and pregnancy, 2) To evaluate the regulation of these pro-apoptotic genes by the luteolytic hormone prostaglandin F2 alpha and 3) To determine whether the anti-apoptotic agent sphingosine-1-phosphate (S1P) will prevent caspase activation and luteolysis of the corpus luteum. The results of the proposed studies will facilitate the design of critical comparative studies to determine the relevance of these apoptotic pathways to the primate CL, and ultimately, clinical syndromes of luteal dysfuntion. To achieve these goals, the research design includes the study of caspases in CL obtained in different stages from cycling and pregnant rats. In addition, caspases will be studied in CL from pregnant rats treated with prostaglandin F2alpha (a luteolytic hormone) and/or sphingosine-1-phosphate (S1P: an antiapoptotic agent). The expression of caspase mRNA in CL will be analyzed by RT- Real Time PCR; and the caspase protein levels, activity and localization in the CL will be studied by Western blots, enzyme assays and ICC. Apoptosis will be measured by TUNEL and electrophoresis in agarose gels. ? ? ?

Agency
National Institute of Health (NIH)
Institute
Fogarty International Center (FIC)
Type
Small Research Grants (R03)
Project #
1R03TW007041-01A2
Application #
7069265
Study Section
International and Cooperative Projects - 1 Study Section (ICP1)
Program Officer
Michels, Kathleen M
Project Start
2006-04-15
Project End
2009-02-28
Budget Start
2006-04-15
Budget End
2007-02-28
Support Year
1
Fiscal Year
2006
Total Cost
$39,372
Indirect Cost
Name
Oregon Health and Science University
Department
Physiology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Hernandez, Fatima; Peluffo, Marina C; Stouffer, Richard L et al. (2011) Role of the DLL4-NOTCH system in PGF2alpha-induced luteolysis in the pregnant rat. Biol Reprod 84:859-65
Hernandez, Fatima; Peluffo, Marina C; Bas, Diana et al. (2009) Local effects of the sphingosine 1-phosphate on prostaglandin F2alpha-induced luteolysis in the pregnant rat. Mol Reprod Dev 76:1153-64
Peluffo, Marina C; Stouffer, Richard L; Tesone, Marta (2007) Activity and expression of different members of the caspase family in the rat corpus luteum during pregnancy and postpartum. Am J Physiol Endocrinol Metab 293:E1215-23