Myositis in Lewis rats induced by the superantigen Staphylococcal enterotoxin A.


Journal

Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 19 03 2019
accepted: 03 05 2019
pubmed: 16 5 2019
medline: 15 2 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

The aetiology of inflammatory myopathies is not clearly known. A predominance of activated Cd8+ T lymphocytes in inflammatory infiltrates has already been detected. Superantigens activate lymphocytes in an oligoclonal manner. In the present investigation, we investigated local effects after injection of the superantigen (Sag) Staphylococcus enterotoxin A (SEA) in the quadriceps femoris muscle of Lewis rats. Histopathology and gene expression profiling was performed after injection of SEA or saline (control group) after one, three and 10 days. Histology revealed focal myositis predominated by Cd8+ T lymphocytes with a perimysial, endomysial and perivascular distribution, peaking 3 days after SEA injection. Using DNA microarray analysis (Affymetrix Rat Genome 230 2.0) genes that were differentially over-expressed at least 15 times at days one, three or ten after SEA injection were further analysed. One day after SEA injection over-expressed genes were related to the immune response (e.g. Fcnb, CD8a) but also to cell proliferation, differentiation and migration (e.g. Mpp2). Three days after SEA injection, differentially overexpressed genes were mainly related to the immune reaction with a clear signature for a Cd8+ T lymphocyte response (e.g. Cd3d, Cd8, Prf1, Gzmb). Ten days after SEA injection, the differentially overexpressed genes were again associated with the immune reaction (e.g. Cd3d, Il2) but also with regenerative processes and wound healing (e.g. Tgfa, Tpm1, Ripply1). The inflammatory response induced by SEA in Lewis rats shares histological and molecular similarities to polymyositis in humans. Therefore, SEA induced myositis can be taken as a new and apt model for polymyositis.

Identifiants

pubmed: 31087247
doi: 10.1007/s11033-019-04858-9
pii: 10.1007/s11033-019-04858-9
doi:

Substances chimiques

Enterotoxins 0
Histocompatibility Antigens Class II 0
Intracellular Signaling Peptides and Proteins 0
Membrane Proteins 0
Superantigens 0
enterotoxin A, Staphylococcal 37337-57-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4085-4094

Subventions

Organisme : Martin Luther University Halle-Wittenberg
ID : FKZ 28/45 Wilhelm-Roux program

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Auteurs

Alexander Emmer (A)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany. alexander.emmer@uk-halle.de.

Abimbola Abobarin-Adeagbo (A)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.

Andreas Posa (A)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.

Berit Jordan (B)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.

Karl-Stefan Delank (KS)

Department of Orthopaedic Surgery, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.

Martin Sebastian Staege (MS)

Department of Surgical and Conservative Paediatrics and Adolescent Medicine, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.

Alexander Surov (A)

Department of Diagnostic and Interventional Radiology, University of Leipzig, Leipzig, Germany.

Stephan Zierz (S)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.

Malte Erich Kornhuber (ME)

Department of Neurology, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.

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Classifications MeSH