7 results match your criteria: "CNRS-Université de Montpellier UMR9002[Affiliation]"

Objective: CCR5, a G protein-coupled receptor (GPCR), is used by most HIV strains as a coreceptor. In this study, we looked for other GPCR able to modify HIV-1 infection.

Design: We analyzed the effects of one GPCR coexpressed with CCR5, EBI2, on HIV-1 replicative cycle.

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Adenomyotic Lesions Are Induced in the Mouse Uterus after Exposure to NSAID and EE2 Mixtures at Environmental Doses.

Int J Mol Sci

February 2024

Développement et Pathologie de la Gonade, Institut de Génétique Humaine, Centre National de la Recherche Scientifique, Université de Montpellier UMR9002, 34090 Montpellier, France.

The aim of this study was to assess the long-term effect of exposure to environmentally relevant doses of non-steroidal anti-inflammatory drugs (NSAIDs; ibuprofen, and diclofenac) and 17β-ethinylestradiol (EE2) on the mouse uterus. NSAID-EE2 mixtures were administered in the drinking water from gestational day 8 until 8 weeks post-birth (i.e.

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Intergenerational effects on fertility in male and female mice after chronic exposure to environmental doses of NSAIDs and 17α-ethinylestradiol mixtures.

Food Chem Toxicol

December 2023

Développement et Pathologie de La Gonade, Institut de Génétique Humaine, Centre National de La Recherche Scientifique, Université de Montpellier UMR9002, Montpellier, France. Electronic address:

Non-steroidal anti-inflammatory drugs (NSAIDs) and 17α-ethinylestradiol (EE2) are extensively used in human and veterinary medicine. Due to their partial removal by wastewater treatment plants, they are frequent environmental contaminants, particularly in drinking water. Here, we investigated the adverse outcomes of chronic exposure to mixtures of NSAIDs (ibuprofen, 2hydroxy-ibuprofen, diclofenac) and EE2 at two environmentally relevant doses in drinking water, on the reproductive organ development and fertility in F1-exposed male and female mice and in their F2 offspring.

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Condensates, the place to hide self-immunostimulatory RNA.

Mol Cell

October 2022

Laboratoire de virologie Moléculaire. Institut de Génétique Humaine, CNRS-Université de Montpellier UMR9002, 141 Rue de la Cardonille, 34296 Montpellier cedex 5, France. Electronic address:

Distinguishing the self from the non-self by the immune system is essential to avoid inflammatory and autoimmune diseases. Maharana et al. (2022) reveal a mechanism for hiding self-immunostimulatory RNA involving a three-variable equation: SAMHD1 and its exonuclease activity, single-stranded RNA, and RNA-protein condensate.

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Regulatory T cell/Th17 balance in the pathogenesis of paediatric Behçet disease.

Rheumatology (Oxford)

December 2021

Département de Biothérapies (CIC-BTi) et Inflammation-Immunopathologie-Biothérapie (I2B), AP-HP, Hôpital La Pitié-Salpêtrière, F-75561, Paris, France.

Objectives: Behçet disease (BD) is a chronic systemic inflammatory disorder of unknown aetiology. The aim of this study was to determine the orientation of T cell subpopulations in paediatric BD and more precisely to look for a regulatory T lymphocyte (Treg)/Th17 imbalance.

Methods: T cell subpopulations were analysed by flow cytometry in the peripheral blood of paediatric patients with acute BD (aBD; n = 24), remitting BD (rBD; n = 12) and in healthy controls (HCs; n = 24).

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The Mouse Microbiome Is Required for Sex-Specific Diurnal Rhythms of Gene Expression and Metabolism.

Cell Metab

February 2019

Department of Diabetes and Circadian Rhythms, Nestlé Institute of Health Sciences, 1015 Lausanne, Switzerland; School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland. Electronic address:

The circadian clock and associated feeding rhythms have a profound impact on metabolism and the gut microbiome. To what extent microbiota reciprocally affect daily rhythms of physiology in the host remains elusive. Here, we analyzed transcriptome and metabolome profiles of male and female germ-free mice.

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Reversing HIV latency via sphingosine-1-phosphate receptor 1 signaling.

AIDS

November 2017

aInstitut de Génétique Humaine, CNRS-Université de Montpellier UMR9002 bARPEGE Pharmacology Screening Interactome platform facility, Institut de Génomique Fonctionnelle, Montpellier cLaboratoire coopératif SPLICOS SAS, IGMM-CNRS-UMR5535, Montpellier dInstitut de Génomique Fonctionnelle, CNRS-UMR5203, INSERM-U661, Université de Montpellier eInstitut de Génétique Moléculaire de Montpellier, CNRS-UMR 5535, Université de Montpellier fUniversité de Montpellier, Montpellier gCentre Hospitalier Universitaire Carémeau, UF d'Immunologie, Nîmes, France.

Objective: In this study, we looked for a new family of latency reversing agents.

Design: We searched for G-protein-coupled receptors (GPCR) coexpressed with the C-C chemokine receptor type 5 (CCR5) in primary CD4 T cells that activate infected cells and boost HIV production.

Methods: GPCR coexpression was unveiled by reverse transcriptase-PCR.

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