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Critical Care

, 16:P99 | Cite as

Corticosteroid resistance in sepsis is influenced by microRNA-124-induced downregulation of glucocorticoid receptor-α

  • P Möhnle
  • C Ledderose
  • J Briegel
  • S Kreth
Poster presentation

Keywords

Glucocorticoid Sepsis Patient Glucocorticoid Resistance Dominant Negative Inhibitor Corticosteroid Resistance 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Background

Acquired glucocorticoid resistance frequently complicates the therapy of sepsis. It leads to an exaggerated proinflammatory response and has been related to altered expression profiles of glucocorticoid receptor isoforms glucocorticoid receptor-α (mediating anti-inflammatory effects) and glucocorticoid receptor-β (acting as a dominant negative inhibitor). We investigated the impact of glucocorticoid receptor isoforms on glucocorticoid effects in human T cells. We hypothesized that changes of the ratio of glucocorticoid receptor isoforms impact glucocorticoid resistance and that glucocorticoid receptor-α expression is controlled by microRNA-mediated gene silencing.

Methods

First, T cells from healthy volunteers (native and CD3/CD28-stimulated cells with or without addition of hydrocortisone) were analyzed for the expression of glucocorticoid receptor isoforms by quantitative PCR. Additionally, effects of gene silencing of glucocorticoid receptor-β by siRNA transfection were determined. Secondly, microRNA-mediated silencing was evaluated by cloning of a glucocorticoid receptor-α-specific 3'-untranslated-region reporter construct and subsequent transfection experiments in cell cultures. Effects of miRNA transfection on glucocorticoid receptor-α expression were analyzed in Jurkat T cells and in T cells from healthy volunteers (quantitative PCR and western blotting). Finally, expression of glucocorticoid receptor-α, glucocorticoid receptor-β, and miR-124 was tested in T cells of sepsis patients (n = 24).

Results

Stimulation of T cells induced a significant upregulation of glucocorticoid receptor-α (not glucocorticoid receptor-β), thereby possibly rendering T cells more sensitive to glucocorticoids; this T-cell response was hindered by hydrocortisone. Silencing of glucocorticoid receptor-β doubled the inhibitory effects of glucocorticoids on IL-2 production. MicroRNA-124 was proved to specifically downregulate glucocorticoid receptor-α. Furthermore, a glucocorticoid-induced threefold upregulation of microRNA-124 was found. T cells of sepsis patients exhibited slightly decreased glucocorticoid receptor-α and slightly increased miR-124 expression levels, whereas glucocorticoid receptor-β expression was twofold upregulated (P < 0.01) and exhibited a remarkable interindividual variability.

Conclusion

Glucocorticoid treatment induces expression of miR-124, which downregulates glucocorticoid receptor-α thereby limiting anti-inflammatory effects of glucocorticoids. Steroid treatment might aggravate glucocorticoid resistance in patients with high glucocorticoid receptor-β levels.

Notes

Acknowledgements

This work has recently been published in Critical Care Medicine: Ledderose C, Möhnle P, Limbeck E, Schütz S, Weis F, Rink J, Briegel J, Kreth S: Corticosteroid resistance in sepsis is influenced by microRNA-124-induced downregulation of glucocorticoid receptor-α. Crit Care Med 2012 [Epub ahead of print]. © Society of Critical Care Medicine and Lippincott Williams & Wilkins, and the presented excerpt for Sepsis 2012 Paris was permitted by Wolters Kluwer Health, 8 August 2012.

Copyright information

© Möhnle et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Authors and Affiliations

  • P Möhnle
    • 1
  • C Ledderose
    • 2
  • J Briegel
    • 1
  • S Kreth
    • 1
  1. 1.Ludwig-Maximilians-Universität München, Klinik für AnaesthesiologieMünchenGermany
  2. 2.Universitätsklinikum Mannheim, Klinik für Anästhesiologie und IntensivmedizinMannheimGermany

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