SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

Metformin attenuates the effect of Staphylococcus aureus on airway tight junctions by increasing PKCζ-mediated phosphorylation of occludin.

Kalsi, KK; Garnett, JP; Patkee, W; Weekes, A; Dockrell, ME; Baker, EH; Baines, DL (2018) Metformin attenuates the effect of Staphylococcus aureus on airway tight junctions by increasing PKCζ-mediated phosphorylation of occludin. J Cell Mol Med, 23 (1). pp. 317-327. ISSN 1582-4934 https://doi.org/10.1111/jcmm.13929
SGUL Authors: Baines, Deborah Baker, Emma Harriet Kalsi, Kameljit Kaur

[img]
Preview
PDF Published Version
Available under License Creative Commons Attribution.

Download (1MB) | Preview
[img]
Preview
["document_typename_cannot open `/data/SGUL/sgul/eprints3/archives/sgul/documents/disk0/00/11/01/44/01/Journal' (No such file or directory) cannot open `of' (No such file or directory) cannot open `cellular' (No such file or directory) cannot open `molecular' (No such file o" not defined] Accepted Version
Available under License Creative Commons Attribution.

Download (1MB) | Preview

Abstract

Airway epithelial tight junction (TJ) proteins form a resistive barrier to the external environment, however, during respiratory bacterial infection TJs become disrupted compromising barrier function. This promotes glucose flux/accumulation into the lumen which acts as a nutrient source for bacterial growth. Metformin used for the treatment of diabetes increases transepithelial resistance (TEER) and partially prevents the effect of bacteria but the mechanisms of action are unclear. We investigated the effect of metformin and Staphylococcus aureus on TJ proteins, zonula occludins (ZO)-1 and occludin in human airway epithelial cells (H441). We also explored the role of AMP-activated protein kinase (AMPK) and PKCζ in metformin-induced effects. Pretreatment with metformin prevented the S. aureus-induced changes in ZO-1 and occludin. Metformin also promoted increased abundance of full length over smaller cleaved occludin proteins. The nonspecific PKC inhibitor staurosporine reduced TEER but did not prevent the effect of metformin indicating that the pathway may involve atypical PKC isoforms. Investigation of TJ reassembly after calcium depletion showed that metformin increased TEER more rapidly and promoted the abundance and localization of occludin at the TJ. These effects were inhibited by the AMPK inhibitor, compound C and the PKCζ pseudosubstrate inhibitor (PSI). Metformin increased phosphorylation of occludin and acetyl-coA-carboxylase but only the former was prevented by PSI. This study demonstrates that metformin improves TJ barrier function by promoting the abundance and assembly of full length occludin at the TJ and that this process involves phosphorylation of the protein via an AMPK-PKCζ pathway.

Item Type: Article
Additional Information: © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Staphylococcus aureus, PKCζ, ZO-1, airway epithelium, metformin, occludin, respiratory infection, tight junctions, 0304 Medicinal And Biomolecular Chemistry, 0601 Biochemistry And Cell Biology, 1103 Clinical Sciences, Biochemistry & Molecular Biology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: J Cell Mol Med
ISSN: 1582-4934
Language: eng
Dates:
DateEvent
27 December 2018Published
18 November 2018Published Online
29 August 2018Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/K012770/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
PubMed ID: 30450773
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110144
Publisher's version: https://doi.org/10.1111/jcmm.13929

Actions (login required)

Edit Item Edit Item