Local steroid activation is a critical mediator of the anti-inflammatory actions of therapeutic glucocorticoids.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
02 2021
Historique:
received: 02 07 2020
revised: 05 10 2020
accepted: 06 10 2020
pubmed: 10 11 2020
medline: 18 2 2021
entrez: 9 11 2020
Statut: ppublish

Résumé

The enzyme 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) plays a well-characterised role in the metabolism and activation of endogenous glucocorticoids (GCs). However, despite its potent upregulation at sites of inflammation, its role in peripheral metabolism and action of therapeutic GCs remains poorly understood. We investigated the contribution of 11β-HSD1 to the anti-inflammatory properties of the active GC corticosterone, administered at therapeutic doses in murine models of polyarthritis. Using the tumour necrosis factor-tg and K/BxN serum-induced models of polyarthritis, we examined the anti-inflammatory properties of oral administration of corticosterone in animals with global, myeloid and mesenchymal targeted transgenic deletion of 11β-HSD1. Disease activity and joint inflammation were scored daily. Joint destruction and measures of local and systemic inflammation were determined by histology, micro-CT, quantitative RT-PCR, fluorescence activated cell sorting and ELISA. Global deletion of 11β-HSD1 resulted in a profound GC resistance in animals receiving corticosterone, characterised by persistent synovitis, joint destruction and inflammatory leucocyte infiltration. This was partially reproduced with myeloid, but not mesenchymal 11β-HSD1 deletion, where paracrine GC signalling between cell populations was shown to overcome targeted deletion of 11β-HSD1. We identify an entirely novel component of therapeutic GC action, whereby following their systemic metabolism, they require peripheral reactivation and amplification by 11β-HSD1 at sites of inflammation to deliver their anti-inflammatory therapeutic effects. This study provides a novel mechanistic understanding of the anti-inflammatory properties of therapeutic GCs and their targeting to sites of inflammation in polyarthritis.

Identifiants

pubmed: 33162397
pii: annrheumdis-2020-218493
doi: 10.1136/annrheumdis-2020-218493
pmc: PMC7815637
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Glucocorticoids 0
11-beta-Hydroxysteroid Dehydrogenase Type 1 EC 1.1.1.146
Corticosterone W980KJ009P

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

250-260

Subventions

Organisme : Versus Arthritis
ID : 19859
Pays : United Kingdom
Organisme : Versus Arthritis
ID : 20843
Pays : United Kingdom
Organisme : Versus Arthritis
ID : 21743
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P021220/1
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Chloe Fenton (C)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.

Claire Martin (C)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.

Rachel Jones (R)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
MRC Arthritis Research UK Centre for Musculoskeletal Ageing Research, University of Birmingham Edgbaston Campus, Birmingham, UK.

Adam Croft (A)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.

Joana Campos (J)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.

Amy J Naylor (AJ)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Centre for Translational Inflammation Research, University of Birmingham, Birmingham, UK.

Angela E Taylor (AE)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
Centre for Endocrinology, Diabetes and Metabolism, University of Birmingham, Birmingham, UK.

Myriam Chimen (M)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Institute for Clinical Sciences, University of Birmingham, Birmingham, UK.

Mark Cooper (M)

ANZAC Research Institute, The University of Sydney, Sydney, New South Wales, Australia.

Gareth G Lavery (GG)

Institute for Metabolism and Systems Research, University of Birmingham, Birmingham, UK.
MRC Arthritis Research UK Centre for Musculoskeletal Ageing Research, University of Birmingham Edgbaston Campus, Birmingham, UK.
Centre for Endocrinology, Diabetes and Metabolism, University of Birmingham, Birmingham, UK.

Karim Raza (K)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, UK.

Rowan S Hardy (RS)

Research into Inflammatory Arthritis Centre, Versus Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK R.Hardy@bham.ac.uk.
MRC Arthritis Research UK Centre for Musculoskeletal Ageing Research, University of Birmingham Edgbaston Campus, Birmingham, UK.
Institute for Clinical Sciences, University of Birmingham, Birmingham, UK.

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Classifications MeSH