Publications by authors named "P ROUAULT"

Article Synopsis
  • Under neuroinflammatory conditions, astrocytes adopt a reactive phenotype that exacerbates inflammation and contributes to neurodegeneration, with the study focusing on the role of astrocytic DLL4 and its interaction with NOTCH1 in regulating this reactivity.
  • The research found that during neuroinflammation, DLL4 is upregulated in both mice and humans, leading to increased astrocyte reactivity, blood-brain barrier permeability, and inflammatory responses through the DLL4-NOTCH1 signaling pathway.
  • Blocking DLL4 with antibodies showed promise in alleviating symptoms of experimental autoimmune encephalomyelitis in mice, suggesting a new potential therapeutic approach for treating CNS autoimmune diseases.
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Short-term fecal pollution events are a major challenge for managing microbial safety at recreational waters. Long turn-over times of current laboratory methods for analyzing fecal indicator bacteria (FIB) delay water quality assessments. Data-driven models have been shown to be valuable approaches to enable fast water quality assessments.

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Background: Heart failure with preserved ejection fraction is proposed to be caused by endothelial dysfunction in cardiac microvessels. Our goal was to identify molecular and cellular mechanisms underlying the development of cardiac microvessel disease and diastolic dysfunction in the setting of type 2 diabetes.

Methods: We used (leptin receptor-deficient) female mice as a model of type 2 diabetes and heart failure with preserved ejection fraction and identified Hhipl1 (hedgehog interacting protein-like 1), which encodes for a decoy receptor for HH (hedgehog) ligands as a gene upregulated in the cardiac vascular fraction of diseased mice.

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Background Although the critical role of pericytes in maintaining vascular integrity has been extensively demonstrated in the brain and the retina, little is known about their role in the heart. We aim to investigate structural and functional consequences of partial pericyte depletion (≈60%) in the heart of adult mice. Methods and Results To deplete pericytes in adult mice, we used platelet-derived growth factor receptor β-Cre/ERT2; Rosa mice and compared their phenotype with that of control mice (Rosa) chosen among their littermates.

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To understand the fine differential elements that can lead to or prevent acute respiratory distress syndrome (ARDS) in COVID-19 patients, it is crucial to investigate the immune response architecture. We herein dissected the multiple layers of B cell responses by flow cytometry and Ig repertoire analysis from acute phase to recovery. Flow cytometry with FlowSOM analysis showed major changes associated with COVID-19 inflammation such as an increase of double-negative B-cells and ongoing plasma cell differentiation.

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