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Grant: Discovery Grants Program - Individual

Université du Québec à Trois-Rivières

$42,809.00

Regulation of cell survival in the rat uterus

EF 2009-10

Résumé
Recognition, maintenance and termination of pregnancy are complex processes involving both maternal and embryonic signals. In the rodents during early implantation, endometrial epithelial cells undergo apoptosis. Later, the stromal cells undergo decidualization, which is followed by decidua basalis (DB) regression, involving apoptosis of decidual cells. At the end of pregnancy, a tightly controlled production of prostaglandins is necessary to induce parturition. However, the molecular mechanisms governing endometrial cell apoptosis are not yet defined. Interestingly, our laboratory has showed that individual TGF-b isoforms (TGF-b1, TGF-b2 and TGF-b3) are differently expressed in the uterus during rat pregnancy: TGF-b1 and TGF-b2 are present during implantation and DB regression, whereas TGF-b3 isoform is only present during DB and parturition. We have also provided evidence that distinct TGF-b isoforms can activate distinct signaling pathways in endometrial cells, since only TGF-b3 induces phosphorylation/activation of Akt in endometrial epithelial cells. In the pregnant rat uterus, multiple TGF-b isoforms are often co-expressed: how distinct TGF-b isoform-activated pathways integrate, and shift the balance towards cell survival or cell death in the pregnant uterus, is poorly understood. The overall and long term objective of the proposed research program is to examine and understand the regulation of expression as well as the endocrine, paracrine and autocrine activity of the TGF-b isoforms in the endometrium during the three important phases of pregnancy: 1) implantation, 2) DB regression, and 3) parturition. The short term objectives of the current proposal are to characterize the involvement, the mechanisms of action and interactions of TGF-b isoforms in the (i) regulation of endometrial epithelial cell death at the time of embryo implantation, (ii) stromal cell-induced apoptosis during decidua DB and (iii) prostaglandins regulation and secretion at the time of parturition. Information gained from these studies will help to understand the importance of TGF-b isoforms during these critical reproductive situations and will provide important clues for successful establishment, maintenance and termination of pregnancy.
Programme
Discovery Grants Program - Individual
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
238501-2008
Name nom
Asselin, Eric
Department département
Chimie-biologie
Organization id
59
Institution établissement
Université du Québec à Trois-Rivières
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2009
Competition year année de concours
2008
Award amount
42809
Program id
RGPIN
Program nane en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1011
Committee name en
Integrative Animal Biology
Committee name fr
Biologie Animale Intégrative
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
5505
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Animal reproduction
Research subject fr
Reproduction animale
Partie
2
Nb partie
5
Application title
Regulation of cell survival in the rat uterus
Keyword
NA
Application summary
Recognition, maintenance and termination of pregnancy are complex processes involving both maternal and embryonic signals. In the rodents during early implantation, endometrial epithelial cells undergo apoptosis. Later, the stromal cells undergo decidualization, which is followed by decidua basalis (DB) regression, involving apoptosis of decidual cells. At the end of pregnancy, a tightly controlled production of prostaglandins is necessary to induce parturition. However, the molecular mechanisms governing endometrial cell apoptosis are not yet defined. Interestingly, our laboratory has showed that individual TGF-b isoforms (TGF-b1, TGF-b2 and TGF-b3) are differently expressed in the uterus during rat pregnancy: TGF-b1 and TGF-b2 are present during implantation and DB regression, whereas TGF-b3 isoform is only present during DB and parturition. We have also provided evidence that distinct TGF-b isoforms can activate distinct signaling pathways in endometrial cells, since only TGF-b3 induces phosphorylation/activation of Akt in endometrial epithelial cells. In the pregnant rat uterus, multiple TGF-b isoforms are often co-expressed: how distinct TGF-b isoform-activated pathways integrate, and shift the balance towards cell survival or cell death in the pregnant uterus, is poorly understood. The overall and long term objective of the proposed research program is to examine and understand the regulation of expression as well as the endocrine, paracrine and autocrine activity of the TGF-b isoforms in the endometrium during the three important phases of pregnancy: 1) implantation, 2) DB regression, and 3) parturition. The short term objectives of the current proposal are to characterize the involvement, the mechanisms of action and interactions of TGF-b isoforms in the (i) regulation of endometrial epithelial cell death at the time of embryo implantation, (ii) stromal cell-induced apoptosis during decidua DB and (iii) prostaglandins regulation and secretion at the time of parturition. Information gained from these studies will help to understand the importance of TGF-b isoforms during these critical reproductive situations and will provide important clues for successful establishment, maintenance and termination of pregnancy.