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      Overexpression of Substance P in pig airways increases MUC5AC through an NF‐kβ pathway

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          Abstract

          Substance P (SP) is a tachykinin that regulates airway mucous secretion in both health and disease. Our study aimed to determine whether overexpression of SP without pre‐existing inflammation was sufficient to induce changes in mucin secretion and transport in small airways. Utilizing porcine precision‐cut lung slices, we measured the impact of AAV‐mediated overexpression of SP on airway physiology ex vivo. Immunofluorescence signal intensity for MUC5AC was significantly increased in SP‐overexpressed precision‐cut lung slices compared to GFP controls. No difference in MUC5B signal intensity between treatments was detected. SP‐overexpressed precision‐cut lung slices also exhibited decreased IL10 mRNA, an important inhibitor of mucous cell metaplasia. Overt deficits in mucociliary transport were not noted, though a trend for decreased mean transport speed was detected in methacholine‐challenged airways overexpressing SP compared to GFP controls. Pharmacologic inhibition of the NF‐kβ pathway abrogated the effects of overexpression of SP on both MUC5AC and IL10. Collectively, these data suggest that overexpression of SP in the absence of existing inflammation increases MUC5AC via activation of the NF‐kβ pathway. Thus, these data further highlight SP as a key driver of abnormal mucous secretion and underscore NF‐kβ signaling as a pathway of potential therapeutic intervention.

          Abstract

          Overexpression of Substance P increased MUC5AC in porcine small airways in the absence of inflammation. The effect was mitigated by the inhibition of the NF‐KB pathway.

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          Most cited references61

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            Airway mucus function and dysfunction.

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              Robust single particle tracking in live cell time-lapse sequences

              Single particle tracking (SPT) is often the rate-limiting step in live cell imaging studies of sub-cellular dynamics. Here we present a tracking algorithm that addresses the principal challenges of SPT, namely high particle density, particle motion heterogeneity, temporary particle disappearance, and particle merging and splitting. The algorithm first links particles between consecutive frames and then links the resulting track segments into complete trajectories. Both steps are formulated as global combinatorial optimization problems whose solution identifies the overall most likely set of particle trajectories throughout the movie. Using this approach, we show that the GTPase dynamin differentially affects the kinetics of long and short-lived endocytic structures, and that the motion of CD36 receptors along cytoskeleton-mediated linear tracks increases their aggregation probability. Both applications indicate the requirement for robust and complete tracking of dense particle fields to dissect the mechanisms of receptor organization at the level of the plasma membrane.
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                Author and article information

                Contributors
                leahreznikov@ufl.edu
                Journal
                Physiol Rep
                Physiol Rep
                10.1002/(ISSN)2051-817X
                PHY2
                physreports
                Physiological Reports
                John Wiley and Sons Inc. (Hoboken )
                2051-817X
                13 February 2021
                February 2021
                : 9
                : 3 ( doiID: 10.1002/phy2.v9.3 )
                : e14749
                Affiliations
                [ 1 ] Department of Physiological Sciences University of Florida Gainesville FL USA
                [ 2 ] Department of Medicinal Chemistry and Center for Natural Products Drug Discovery and Development University of Florida Gainesville FL USA
                Author notes
                [*] [* ] Correspondence

                Leah R. Reznikov, University of Florida, Department of Physiological Sciences, 1333 Center Drive, PO Box 100144, Gainesville, FL 32610, USA.

                Email: leahreznikov@ 123456ufl.edu

                Author information
                https://orcid.org/0000-0002-4074-9070
                Article
                PHY214749
                10.14814/phy2.14749
                7881348
                33580593
                dae5de47-72f2-447a-a238-f5480f4b3712
                © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 January 2021
                : 13 January 2021
                Page count
                Figures: 4, Tables: 0, Pages: 11, Words: 7554
                Funding
                Funded by: National Heart, Lung, and Blood Institute , open-funder-registry 10.13039/100000050;
                Award ID: HL119560
                Funded by: NIH Office of the Director , open-funder-registry 10.13039/100000052;
                Award ID: 1OT2OD026582
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                February 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.7 mode:remove_FC converted:13.02.2021

                muc5ac,muc5b,neuropeptides,tachykinins
                muc5ac, muc5b, neuropeptides, tachykinins

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