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      Quercetin improves and protects Calu-3 airway epithelial barrier function

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          Abstract

          Introduction: In light of the impact of airway barrier leaks in COVID-19 and the significance of vitamin D in COVID-19 outcomes, including airway barrier protection, we investigated whether the very common dietary flavonoid quercetin could also be efficacious in supporting airway barrier function.

          Methods: To address this question, we utilized the widely used airway epithelial cell culture model, Calu-3.

          Results: We observed that treating Calu-3 cell layers with quercetin increased transepithelial electrical resistance while simultaneously reducing transepithelial leaks of 14C-D-mannitol (Jm) and 14C-inulin. The effects of quercetin were concentration-dependent and exhibited a biphasic time course. These effects of quercetin occurred with changes in tight junctional protein composition as well as a partial inhibition of cell replication that resulted in decreased linear junctional density. Both of these effects potentially contribute to improved barrier function. Quercetin was equally effective in reducing the barrier compromise caused by the pro-inflammatory cytokine TNF-α, an action that seemed to derive, in part, from reducing the elevation of ERK 1/2 caused by TNF-α.

          Discussion: Quercetin improved Calu-3 barrier function and reduced TNF-α-induced barrier compromise, mediated in part by changes in the tight junctional complex.

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          Review of the biology of quercetin and related bioflavonoids

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            Der p 1 facilitates transepithelial allergen delivery by disruption of tight junctions.

            House dust mite (HDM) allergens are important factors in the increasing prevalence of asthma. The lung epithelium forms a barrier that allergens must cross before they can cause sensitization. However, the mechanisms involved are unknown. Here we show that the cysteine proteinase allergen Der p 1 from fecal pellets of the HDM Dermatophagoides pteronyssinus causes disruption of intercellular tight junctions (TJs), which are the principal components of the epithelial paracellular permeability barrier. In confluent airway epithelial cells, Der p 1 led to cleavage of the TJ adhesion protein occludin. Cleavage was attenuated by antipain, but not by inhibitors of serine, aspartic, or matrix metalloproteinases. Putative Der p 1 cleavage sites were found in peptides from an extracellular domain of occludin and in the TJ adhesion protein claudin-1. TJ breakdown nonspecifically increased epithelial permeability, allowing Der p 1 to cross the epithelial barrier. Thus, transepithelial movement of Der p 1 to dendritic antigen-presenting cells via the paracellular pathway may be promoted by the allergen's own proteolytic activity. These results suggest that opening of TJs by environmental proteinases may be the initial step in the development of asthma to a variety of allergens.
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              Short term, high-dose vitamin D supplementation for COVID-19 disease: a randomised, placebo-controlled, study (SHADE study)

              Vitamin D has an immunomodulatory role but the effect of therapeutic vitamin D supplementation in SARS-CoV-2 infection is not known. Effect of high dose, oral cholecalciferol supplementation on SARS-CoV-2 viral clearance. Randomised, placebo-controlled. Asymptomatic or mildly symptomatic SARS-CoV-2 RNA positive vitamin D deficient (25(OH)D 50 ng/ml (intervention group) or placebo (control group). Patients requiring invasive ventilation or with significant comorbidities were excluded. 25(OH)D levels were assessed at day 7, and cholecalciferol supplementation was continued for those with 25(OH)D 50 ng/ml by day-7 and another two by day-14 [day-14 25(OH)D levels 51.7 (48.9 to 59.5) ng/ml and 15.2 (12.7 to 19.5) ng/ml (p<0.001) in intervention and control group, respectively]. 10 (62.5%) participants in the intervention group and 5 (20.8%) participants in the control arm (p<0.018) became SARS-CoV-2 RNA negative. Fibrinogen levels significantly decreased with cholecalciferol supplementation (intergroup difference 0.70 ng/ml; P=0.007) unlike other inflammatory biomarkers. Greater proportion of vitamin D-deficient individuals with SARS-CoV-2 infection turned SARS-CoV-2 RNA negative with a significant decrease in fibrinogen on high-dose cholecalciferol supplementation. NCT04459247.
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                Author and article information

                Contributors
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                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                23 November 2023
                2023
                : 11
                : 1271201
                Affiliations
                [1] 1 The Lankenau Institute for Medical Research , Wynnewood, PA, United States
                [2] 2 The Departments of Biology and Chemistry, Drexel University , Philadelphia, PA, United States
                [3] 3 The Division of Gastroenterology , The Lankenau Medical Center , Wynnewood, PA, United States
                Author notes

                Edited by: Kapila Seneviratne, University of Kelaniya, Sri Lanka

                Reviewed by: Geetha Samak, DVS College of Arts and Science, India

                Seyedeh Roya Alizadeh, Mazandaran University of Medical Sciences, Iran

                *Correspondence: J. M. Mullin, mullinj@ 123456mlhs.org
                Article
                1271201
                10.3389/fcell.2023.1271201
                10701405
                38078004
                50880e28-cf5b-426b-b511-0ce61e5e3b3c
                Copyright © 2023 DiGuilio, Rybakovsky, Valenzano, Nguyen, Del Rio, Newberry, Spadea and Mullin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 August 2023
                : 07 November 2023
                Funding
                The authors declare that financial support was received for the research, authorship, and/or publication of this article. Funding from the Sharpe Strumia Research Foundation (JMM) supported these studies.
                Categories
                Cell and Developmental Biology
                Original Research
                Custom metadata
                Cell Adhesion and Migration

                quercetin,flavonoid,tight junction,claudin,barrier function,tumor necrosis factor,cell division,calu-3

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