Characterization of acute TLR-7 agonist-induced hemorrhagic myocarditis in mice by multiparametric quantitative cardiac magnetic resonance imaging.


Journal

Disease models & mechanisms
ISSN: 1754-8411
Titre abrégé: Dis Model Mech
Pays: England
ID NLM: 101483332

Informations de publication

Date de publication:
16 08 2019
Historique:
received: 27 05 2019
accepted: 12 07 2019
pubmed: 22 7 2019
medline: 9 4 2020
entrez: 21 7 2019
Statut: epublish

Résumé

Hemorrhagic myocarditis is a potentially fatal complication of excessive levels of systemic inflammation. It has been reported in viral infection, but is also possible in systemic autoimmunity. Epicutaneous treatment of mice with the Toll-like receptor 7 (TLR-7) agonist Resiquimod induces auto-antibodies and systemic tissue damage, including in the heart, and is used as an inducible mouse model of systemic lupus erythematosus (SLE). Here, we show that overactivation of the TLR-7 pathway of viral recognition by Resiquimod treatment of CFN mice induces severe thrombocytopenia and internal bleeding, which manifests most prominently as hemorrhagic myocarditis. We optimized a cardiac magnetic resonance (CMR) tissue mapping approach for the

Identifiants

pubmed: 31324689
pii: dmm.040725
doi: 10.1242/dmm.040725
pmc: PMC6737951
pii:
doi:

Substances chimiques

Imidazoles 0
Toll-Like Receptor 7 0
Iron E1UOL152H7
resiquimod V3DMU7PVXF

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : British Heart Foundation
ID : RG/18/3/33405
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/16/93/32345
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/16/93/32345
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/2/33446
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/14/90/31219
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/17/22/32868
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/14/88/31183
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RM/13/1/30157
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/17/42/33039
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/17/21/32712
Pays : United Kingdom

Informations de copyright

© 2019. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare no competing or financial interests.

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Auteurs

Nicoleta Baxan (N)

Biological Imaging Centre, Department of Medicine, Imperial College London, London W12 0NN, UK.

Angelos Papanikolaou (A)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.

Isabelle Salles-Crawley (I)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.

Amrit Lota (A)

Royal Brompton Hospital, Royal Brompton and Harefield NHS Foundation Trust, London SW3 6NP, UK.

Rasheda Chowdhury (R)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.

Olivier Dubois (O)

Biological Imaging Centre, Department of Medicine, Imperial College London, London W12 0NN, UK.

Jane Branca (J)

The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, USA.

Muneer G Hasham (MG)

The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, USA.

Nadia Rosenthal (N)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.
The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, USA.

Sanjay K Prasad (SK)

Royal Brompton Hospital, Royal Brompton and Harefield NHS Foundation Trust, London SW3 6NP, UK.

Lan Zhao (L)

Biological Imaging Centre, Department of Medicine, Imperial College London, London W12 0NN, UK.
National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.

Sian E Harding (SE)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK.

Susanne Sattler (S)

National Heart and Lung Institute, Imperial College London, London W12 0NN, UK s.sattler@imperial.ac.uk.

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Classifications MeSH