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      Paracellular bicarbonate flux across human cystic fibrosis airway epithelia tempers changes in airway surface liquid pH

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          Abstract

          Key points

          • Cl and HCO 3 had similar paracellular permeabilities in human airway epithelia.

          • P Cl/P Na of airway epithelia was unaltered by pH 7.4  vs. pH 6.0 solutions.

          • Under basal conditions, calculated paracellular HCO 3 flux was secretory.

          • Cytokines that increased airway surface liquid pH decreased or reversed paracellular HCO 3 flux.

          • HCO 3 flux through the paracellular pathway may counterbalance effects of cellular H + and HCO 3 secretion.

          Abstract

          Airway epithelia control the pH of airway surface liquid (ASL), thereby optimizing respiratory defences. Active H + and HCO 3 secretion by airway epithelial cells produce an ASL that is acidic compared with the interstitial space. The paracellular pathway could provide a route for passive HCO 3 flux that also modifies ASL pH. However, there is limited information about paracellular HCO 3 flux, and it remains uncertain whether an acidic pH produced by loss of cystic fibrosis transmembrane conductance regulator anion channels or proinflammatory cytokines might alter the paracellular pathway function. To investigate paracellular HCO 3 transport, we studied differentiated primary cultures of human cystic fibrosis (CF) and non‐CF airway epithelia. The paracellular pathway was pH‐insensitive at pH 6.0 vs. pH 7.4 and was equally permeable to Cl and HCO 3 . Under basal conditions at pH ∼6.6, calculated paracellular HCO 3 flux was weakly secretory. Treating epithelia with IL‐17 plus TNFα alkalinized ASL pH to ∼7.0, increased paracellular HCO 3 permeability, and paracellular HCO 3 flux was negligible. Applying IL‐13 increased ASL pH to ∼7.4 without altering paracellular HCO 3 permeability, and calculated paracellular HCO 3 flux was absorptive. These results suggest that HCO 3 flux through the paracellular pathway counterbalances, in part, changes in the ASL pH produced via cellular mechanisms. As the pH of ASL increases towards that of basolateral liquid, paracellular HCO 3 flux becomes absorptive, tempering the alkaline pH generated by transcellular HCO 3 secretion.

          Key points

          • Cl and HCO 3 had similar paracellular permeabilities in human airway epithelia.

          • P Cl/P Na of airway epithelia was unaltered by pH 7.4  vs. pH 6.0 solutions.

          • Under basal conditions, calculated paracellular HCO 3 flux was secretory.

          • Cytokines that increased airway surface liquid pH decreased or reversed paracellular HCO 3 flux.

          • HCO 3 flux through the paracellular pathway may counterbalance effects of cellular H + and HCO 3 secretion.

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          Most cited references80

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          G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences

          G*Power (Erdfelder, Faul, & Buchner, 1996) was designed as a general stand-alone power analysis program for statistical tests commonly used in social and behavioral research. G*Power 3 is a major extension of, and improvement over, the previous versions. It runs on widely used computer platforms (i.e., Windows XP, Windows Vista, and Mac OS X 10.4) and covers many different statistical tests of the t, F, and chi2 test families. In addition, it includes power analyses for z tests and some exact tests. G*Power 3 provides improved effect size calculators and graphic options, supports both distribution-based and design-based input modes, and offers all types of power analyses in which users might be interested. Like its predecessors, G*Power 3 is free.
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            Principles and standards for reporting animal experiments in The Journal of Physiology and Experimental Physiology.

            The Journal of Physiology and Experimental Physiology have always used UK legislation as the basis of their policy on ethical standards in experiments on non-human animals. However, for international journals with authors, editors and referees from outside the UK the policy can lack transparency and is sometimes cumbersome, requiring the intervention of a Senior Ethics Reviewer or advice from external experts familiar with UK legislation. The journals have therefore decided to set out detailed guidelines for how authors should report experimental procedures that involve animals. As well as helping authors, this new clarity will facilitate the review process and decision making where there are questions regarding animal ethics.
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              Inflammation in cystic fibrosis lung disease: Pathogenesis and therapy.

              Lung disease is the major cause of morbidity and mortality in patients with cystic fibrosis (CF). Although CF lung disease is primarily an infectious disorder, the associated inflammation is both intense and ineffective at clearing pathogens. Persistent high-intensity inflammation leads to permanent structural damage of the CF airways and impaired lung function that eventually results in respiratory failure and death. Several defective inflammatory responses have been linked to cystic fibrosis transmembrane conductance regulator (CFTR) deficiency including innate and acquired immunity dysregulation, cell membrane lipid abnormalities, various transcription factor signaling defects, as well as altered kinase and toll-like receptor responses. The inflammation of the CF lung is dominated by neutrophils that release oxidants and proteases, particularly elastase. Neutrophil elastase in the CF airway secretions precedes the appearance of bronchiectasis, and correlates with lung function deterioration and respiratory exacerbations. Anti-inflammatory therapies are therefore of particular interest for CF lung disease but must be carefully studied to avoid suppressing critical elements of the inflammatory response and thus worsening infection. This review examines the role of inflammation in the pathogenesis of CF lung disease, summarizes the results of past clinical trials and explores promising new anti-inflammatory options.
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                Author and article information

                Contributors
                ian-thornell@uiowa.edu
                michael-welsh@uiowa.edu
                Journal
                J Physiol
                J Physiol
                10.1111/(ISSN)1469-7793
                TJP
                jphysiol
                The Journal of Physiology
                John Wiley and Sons Inc. (Hoboken )
                0022-3751
                1469-7793
                24 July 2020
                01 October 2020
                24 July 2020
                : 598
                : 19 ( doiID: 10.1113/tjp.v598.19 )
                : 4307-4320
                Affiliations
                [ 1 ] Department of Internal Medicine Pappajohn Biomedical Institute Roy J. and Lucille A. Carver College of Medicine University of Iowa Iowa City IA USA
                [ 2 ] Department of Molecular Physiology and Biophysics Pappajohn Biomedical Institute Roy J. and Lucille A. Carver College of Medicine University of Iowa Iowa City IA USA
                [ 3 ] Howard Hughes Medical Institute University of Iowa Iowa City IA USA
                Author notes
                [*] [* ] Correspondence author I. M. Thornell: Department of Internal Medicine, Iowa City, IA 52242 USA. Email:  ian-thornell@ 123456uiowa.edu

                M. J. Welsh: Department of Internal Medicine, Iowa City, IA 52242 USA. Email:  michael-welsh@ 123456uiowa.edu

                Author information
                https://orcid.org/0000-0001-5535-2925
                https://orcid.org/0000-0002-1646-6206
                Article
                TJP14249
                10.1113/JP280120
                7589346
                32627187
                c74cc9af-b5e1-4b55-bffe-d6f1b7ba8752
                © 2020 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 06 May 2020
                : 22 June 2020
                Page count
                Figures: 5, Tables: 3, Pages: 14, Words: 9009
                Categories
                Research Paper
                Molecular and Cellular
                Custom metadata
                2.0
                1 October 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.3 mode:remove_FC converted:27.10.2020

                Human biology
                airway,bicarbonate,epithelia,ion transport
                Human biology
                airway, bicarbonate, epithelia, ion transport

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