Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats

Tankyrases are physiological regulators of Axin, a protein involved in several cellular processes, including Wnt signaling. Here, we investigated the effect of a specific Tankyrase inhibitor (XAV939) in follicular-luteal dynamics, and its possible relationship with ovarian vascular development. Stud...

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Publicado: 2017
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1040452X_v84_n8_p719_Accialini
http://hdl.handle.net/20.500.12110/paper_1040452X_v84_n8_p719_Accialini
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spelling paper:paper_1040452X_v84_n8_p719_Accialini2023-06-08T16:00:47Z Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats luteinization progesterone steroidogenesis Tankyrase inhibitor Wnt/β-catenin 7,8 dihydro 2 [4 (trifluoromethyl)phenyl] 5h thiopyrano[4,3 d]pyrimidin 4 ol beta catenin gonadotropin mitogen activated protein kinase progesterone protein kinase B steroidogenic acute regulatory protein tankyrase vasculotropin Wnt protein beta catenin gonadotropin progesterone tankyrase Wnt protein angiogenesis animal experiment animal tissue antral follicle apoptosis Article cell proliferation controlled study corpus luteum enzyme inhibition enzyme phosphorylation female in vivo study luteal cell nonhuman ovary follicle development priority journal progesterone blood level rat steroidogenesis Wnt signaling pathway animal antagonists and inhibitors corpus luteum metabolism physiology signal transduction Animals beta Catenin Corpus Luteum Female Gonadotropins Progesterone Rats Signal Transduction Tankyrases Wnt Proteins Tankyrases are physiological regulators of Axin, a protein involved in several cellular processes, including Wnt signaling. Here, we investigated the effect of a specific Tankyrase inhibitor (XAV939) in follicular-luteal dynamics, and its possible relationship with ovarian vascular development. Studies were designed to analyze the effect of intrabursa administration of XAV939 in gonadotropin-treated prepubertal rats. In particular, we examined follicle and corpus luteum development, steroidogenesis, angiogenic markers, and apoptotic parameters. We found that in vivo inhibition of Wnt signaling impaired corpus luteum development, with a decrease in the number of corpora lutea balanced by a high number of cysts; decreased circulating progesterone levels, likely due to a decrease in Steroidogenic acute regulatory protein content in the corpus luteum; and increased pro-apoptotic parameters. In addition, Extracellular signal-regulated kinase phosphorylation, Vascular endothelium growth factor 120 content, and endothelial cell area were diminished in corpora lutea of inhibitor-treated ovaries. Thus, Wnt/β-catenin signaling appears to participate in the regulation of corpus luteum development and luteal cell function. © 2017 Wiley Periodicals, Inc. 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1040452X_v84_n8_p719_Accialini http://hdl.handle.net/20.500.12110/paper_1040452X_v84_n8_p719_Accialini
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic luteinization
progesterone
steroidogenesis
Tankyrase inhibitor
Wnt/β-catenin
7,8 dihydro 2 [4 (trifluoromethyl)phenyl] 5h thiopyrano[4,3 d]pyrimidin 4 ol
beta catenin
gonadotropin
mitogen activated protein kinase
progesterone
protein kinase B
steroidogenic acute regulatory protein
tankyrase
vasculotropin
Wnt protein
beta catenin
gonadotropin
progesterone
tankyrase
Wnt protein
angiogenesis
animal experiment
animal tissue
antral follicle
apoptosis
Article
cell proliferation
controlled study
corpus luteum
enzyme inhibition
enzyme phosphorylation
female
in vivo study
luteal cell
nonhuman
ovary follicle development
priority journal
progesterone blood level
rat
steroidogenesis
Wnt signaling pathway
animal
antagonists and inhibitors
corpus luteum
metabolism
physiology
signal transduction
Animals
beta Catenin
Corpus Luteum
Female
Gonadotropins
Progesterone
Rats
Signal Transduction
Tankyrases
Wnt Proteins
spellingShingle luteinization
progesterone
steroidogenesis
Tankyrase inhibitor
Wnt/β-catenin
7,8 dihydro 2 [4 (trifluoromethyl)phenyl] 5h thiopyrano[4,3 d]pyrimidin 4 ol
beta catenin
gonadotropin
mitogen activated protein kinase
progesterone
protein kinase B
steroidogenic acute regulatory protein
tankyrase
vasculotropin
Wnt protein
beta catenin
gonadotropin
progesterone
tankyrase
Wnt protein
angiogenesis
animal experiment
animal tissue
antral follicle
apoptosis
Article
cell proliferation
controlled study
corpus luteum
enzyme inhibition
enzyme phosphorylation
female
in vivo study
luteal cell
nonhuman
ovary follicle development
priority journal
progesterone blood level
rat
steroidogenesis
Wnt signaling pathway
animal
antagonists and inhibitors
corpus luteum
metabolism
physiology
signal transduction
Animals
beta Catenin
Corpus Luteum
Female
Gonadotropins
Progesterone
Rats
Signal Transduction
Tankyrases
Wnt Proteins
Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
topic_facet luteinization
progesterone
steroidogenesis
Tankyrase inhibitor
Wnt/β-catenin
7,8 dihydro 2 [4 (trifluoromethyl)phenyl] 5h thiopyrano[4,3 d]pyrimidin 4 ol
beta catenin
gonadotropin
mitogen activated protein kinase
progesterone
protein kinase B
steroidogenic acute regulatory protein
tankyrase
vasculotropin
Wnt protein
beta catenin
gonadotropin
progesterone
tankyrase
Wnt protein
angiogenesis
animal experiment
animal tissue
antral follicle
apoptosis
Article
cell proliferation
controlled study
corpus luteum
enzyme inhibition
enzyme phosphorylation
female
in vivo study
luteal cell
nonhuman
ovary follicle development
priority journal
progesterone blood level
rat
steroidogenesis
Wnt signaling pathway
animal
antagonists and inhibitors
corpus luteum
metabolism
physiology
signal transduction
Animals
beta Catenin
Corpus Luteum
Female
Gonadotropins
Progesterone
Rats
Signal Transduction
Tankyrases
Wnt Proteins
description Tankyrases are physiological regulators of Axin, a protein involved in several cellular processes, including Wnt signaling. Here, we investigated the effect of a specific Tankyrase inhibitor (XAV939) in follicular-luteal dynamics, and its possible relationship with ovarian vascular development. Studies were designed to analyze the effect of intrabursa administration of XAV939 in gonadotropin-treated prepubertal rats. In particular, we examined follicle and corpus luteum development, steroidogenesis, angiogenic markers, and apoptotic parameters. We found that in vivo inhibition of Wnt signaling impaired corpus luteum development, with a decrease in the number of corpora lutea balanced by a high number of cysts; decreased circulating progesterone levels, likely due to a decrease in Steroidogenic acute regulatory protein content in the corpus luteum; and increased pro-apoptotic parameters. In addition, Extracellular signal-regulated kinase phosphorylation, Vascular endothelium growth factor 120 content, and endothelial cell area were diminished in corpora lutea of inhibitor-treated ovaries. Thus, Wnt/β-catenin signaling appears to participate in the regulation of corpus luteum development and luteal cell function. © 2017 Wiley Periodicals, Inc.
title Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
title_short Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
title_full Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
title_fullStr Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
title_full_unstemmed Tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
title_sort tankyrase inhibition regulates corpus luteum development and luteal function in gonadotropin-treated rats
publishDate 2017
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1040452X_v84_n8_p719_Accialini
http://hdl.handle.net/20.500.12110/paper_1040452X_v84_n8_p719_Accialini
_version_ 1768545796841537536