Pascale Crépieux

ORCID: 0000-0002-2712-5271
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About
Contact & Profiles
Research Areas
  • Receptor Mechanisms and Signaling
  • Neuropeptides and Animal Physiology
  • Protein Kinase Regulation and GTPase Signaling
  • Reproductive Biology and Fertility
  • Hypothalamic control of reproductive hormones
  • Sperm and Testicular Function
  • Estrogen and related hormone effects
  • Computational Drug Discovery Methods
  • Monoclonal and Polyclonal Antibodies Research
  • RNA Research and Splicing
  • Gene Regulatory Network Analysis
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Nitric Oxide and Endothelin Effects
  • RNA and protein synthesis mechanisms
  • Growth Hormone and Insulin-like Growth Factors
  • Ovarian function and disorders
  • Neuroendocrine regulation and behavior
  • interferon and immune responses
  • Renin-Angiotensin System Studies
  • Birth, Development, and Health
  • Glycosylation and Glycoproteins Research
  • Autism Spectrum Disorder Research
  • Child Development and Digital Technology
  • PI3K/AKT/mTOR signaling in cancer
  • Hormonal and reproductive studies

Physiologie de la Reproduction et des Comportements
2016-2025

Université de Tours
2015-2025

Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
2020-2025

Inria Saclay - Île de France
2021-2025

Université Paris-Saclay
2021-2025

Laboratoire de Tribologie et Dynamique des Systèmes
2020-2024

École Polytechnique
2020-2024

Centre National de la Recherche Scientifique
2014-2023

Institut Français du Cheval et de l'Équitation
2015-2023

Centre Val de Loire
2019

Abstract We have established transgenic mice expressing the Cre recombinase under control of anti‐Müllerian hormone (AMH) gene promoter. activity and specificity were evaluated by different means. In AMH‐ mice, expression mRNA was confined to testis ovary. crossed with reporter lines offspring exhibited Cre‐mediated recombination only in male, histochemical analysis indicated that occured every Sertoli cells. female, restricted granulosa cells, but protein not evenly active From these...

10.1002/gene.10100 article EN genesis 2002-06-25

Classically, the FSH receptor (FSH-R) mediates its effects through coupling to guanine nucleotide-binding protein alpha S subunit (Galpha(s)) and activation of cAMP/protein kinase A (PKA) signaling pathway. beta-Arrestins are rapidly recruited FSH-activated play key roles in desensitization internalization. Here, we show that FSH-R expressed HEK 293 cells activated ERK by two temporally distinct pathways dependent, respectively, on Galpha(s)/PKA beta-arrestins. Galpha(s)/PKA-dependent was...

10.1210/me.2006-0098 article EN Molecular Endocrinology 2006-08-04

The I kappaB alpha protein is a key molecular target involved in the control of NF-kappaB/Rel transcription factors during viral infection or inflammatory reactions. This NF-kappaB-inhibitory factor regulated by posttranslational phosphorylation and ubiquitination its amino-terminal signal response domain that targets for rapid proteolysis 26S proteasome. In an attempt to identify regulators inhibitory activity, we undertook yeast two-hybrid genetic screen, using end as bait, identified 12...

10.1128/mcb.17.12.7375 article EN Molecular and Cellular Biology 1997-12-01

In addition to their role in desensitization and internalization of G protein-coupled receptors (GPCRs), β-arrestins are essential scaffolds linking GPCRs Erk1/2 signaling. However, GPCR-operated activation differs between the underlying mechanism remains poorly characterized. Here, we show that serotonin 5-HT2C receptors, which engage pathway via a β-arrestin-dependent mechanism, promotes MEK-dependent β-arrestin2 phosphorylation at Thr383, necessary step for Erk recruitment...

10.7554/elife.23777 article EN cc-by eLife 2017-02-07

Article26 June 2012Open Access Competing G protein-coupled receptor kinases balance protein and β-arrestin signaling Domitille Heitzler BIOS Group, INRA, UMR85, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France CNRS, UMR7247, Université François Rabelais, Tours, IFCE, Contraintes Team, INRIA Paris-Rocquencourt, Le Chesnay, Search for more papers by this author Guillaume Durand Nathalie Gallay Aurélien Rizk Seungkirl Ahn Department of Medicine, Duke University...

10.1038/msb.2012.22 article EN cc-by-nc-nd Molecular Systems Biology 2012-01-01

Gonadotropin receptors belong to the super family of G protein-coupled and mediate physiological effects follicle-stimulating hormone (FSHR) luteinizing (LHR). Their central role in control reproductive function has made them focus intensive studies. Upon binding their cognate hormone, they trigger complex signaling trafficking mechanisms that are tightly regulated concentration, time, space. Classical cellular assays often fail capture all these dynamics. Here, we describe use various...

10.3389/fendo.2015.00130 article EN cc-by Frontiers in Endocrinology 2015-08-27

Intracellular variable fragments from heavy-chain only antibodies of camelids (intra-VHH) have been successfully used for their stabilizing properties to solve the 3D structure active G protein-coupled receptors (GPCRs) bound cognate transducers. They also provide tools link a given conformation GPCR signalling network engaged, thus allowing extensive structure/activity studies. Recently, they instrumental in tracking GPCRs various subcellular compartments. Here, we report isolation and...

10.1101/2025.02.13.638052 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2025-02-17

Abstract β-arrestins serve as signaling scaffolds downstream of G protein-coupled receptors and thus play a crucial role in plethora cellular processes. Although it is largely accepted that the ability to interact simultaneously with many protein partners key protein-independent GPCRs, only precise knowledge these multimeric arrangements will allow full understanding dynamics interactions their functional consequences. However, current experimental procedures for determination...

10.1038/srep10760 article EN cc-by Scientific Reports 2015-06-01

The organismal roles of the ubiquitously expressed class I PI3K isoform p110β remain largely unknown. Using a new kinase-dead knockin mouse model that mimics constitutive pharmacological inactivation p110β, we document full leads to embryonic lethality in substantial fraction mice. Interestingly, homozygous mice survive into adulthood (maximum ~26% on mixed genetic background) have no apparent phenotypes, other than subfertility females and complete infertility males. Systemic inhibition...

10.1371/journal.pgen.1005304 article EN cc-by PLoS Genetics 2015-07-01

<title>Abstract</title> Autism spectrum disorders (ASD) are complex, polygenic and heterogenous neurodevelopmental conditions, imposing a substantial economic burden. ASD genetics is influenced by the environment, specifically social experience during critical period. Despite efficacy of early behavioral interventions targeting specific behaviors in some autistic children, there currently no sustainable treatment for two core symptoms: deficits interaction communication, stereotyped or...

10.21203/rs.3.rs-3759429/v1 preprint EN cc-by Research Square (Research Square) 2024-01-05

Deglycosylated FSH is known to trigger poor Galphas coupling while efficiently binding its receptor. In the present study, we tested possibility that a deglycosylated equine LH (eLHdg) might be able selectively activate beta-arrestin-dependent signaling. We compared native eLH an derivative [i.e. truncated eLHbeta (Delta121-149) combined with asparagine56-deglycosylated eLHalpha (eLHdg)] previously reported as antagonist of cAMP accumulation at receptor (FSH-R). confirmed that, when used in...

10.1210/me.2009-0347 article EN Molecular Endocrinology 2010-01-28
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