Leukocyte TNFR1 and TNFR2 Expression Contributes to the Peripheral Immune Response in Cases with Ischemic Stroke.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
09 04 2021
Historique:
received: 24 02 2021
revised: 24 03 2021
accepted: 01 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 21 10 2021
Statut: epublish

Résumé

Tumor necrosis factor receptor 1 and 2 (TNFR1 and TNFR2) have been found in brain parenchyma of stroke patients, and plasma levels are increased in the acute phase of stroke. We evaluated associations between TNFR1 and TNFR2 plasma levels and stroke severity, infarct size, and functional outcome. Furthermore, we examined cellular expression of TNFR1 and TNFR2 on leukocyte subpopulations to explore the origin of the increased receptor levels. Blood samples were taken from 33 acute ischemic stroke patients and 10 healthy controls. TNFR1 and TNFR2 plasma concentrations were measured and correlated against the Scandinavian Stroke Scale at admission, infarct volume, and the modified Rankin Scale score three months after stroke onset. Classical, intermediate, and non-classical monocytes as well as neutrophils were purified, and cellular expression of TNFR1 and TNFR2 was examined using flow cytometry. TNFR1 and TNFR2 plasma levels were both increased after ischemic stroke, but we found no correlation with patient outcome measurements. Compared to healthy controls, ischemic stroke patients had decreased non-classical monocyte and neutrophil populations expressing TNFR1 and increased neutrophils expressing TNFR2, and decreased non-classical populations co-expressing both TNFR1 and TNFR2. This study supports the hypothesis of an acute immunological response orchestrated by the peripheral immune system following an ischemic stroke. However, the origin of the increased TNFR1 and TNFR2 plasma levels could not be clearly linked to peripheral monocytes or neutrophils. Future studies are needed and will help clarify the potential role as treatment target.

Identifiants

pubmed: 33918875
pii: cells10040861
doi: 10.3390/cells10040861
pmc: PMC8069317
pii:
doi:

Substances chimiques

Glial Fibrillary Acidic Protein 0
Intercellular Signaling Peptides and Proteins 0
Interleukin-6 0
Neurofilament Proteins 0
Receptors, CCR2 0
Receptors, Tumor Necrosis Factor, Type I 0
Receptors, Tumor Necrosis Factor, Type II 0
TNFRSF1A protein, human 0
TNFRSF1B protein, human 0
neurofilament protein L 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : The Danish Society for Neuroscience
ID : NA
Organisme : Odense Universitetshospital
ID : NA
Organisme : Max Th. Harding Larsens Fond
ID : NA
Organisme : Fonden til Lægevidenskabens Fremme
ID : NA
Organisme : Overlægerådets Forskningsfond, Odense University Hospital
ID : NA

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Auteurs

Rikke B Hansen (RB)

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Department of Neurology, Odense University Hospital, 5000 Odense, Denmark.

Cathrine C H Laursen (CCH)

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Brain Research-Inter-Disciplinary Guided Excellence (BRIDGE), Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.

Niala Nawaz (N)

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Department of Neurology, Odense University Hospital, 5000 Odense, Denmark.

Jonna S Madsen (JS)

Department of Biochemistry and Immunology, Lillebaelt Hospital, University Hospital of Southern Denmark, 7100 Vejle, Denmark.
Department of Regional Health Research, University of Southern Denmark, 5000 Odense, Denmark.

Helle H Nielsen (HH)

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Department of Neurology, Odense University Hospital, 5000 Odense, Denmark.
Brain Research-Inter-Disciplinary Guided Excellence (BRIDGE), Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.

Christina Kruuse (C)

Department of Clinical Medicine, University of Copenhagen, 2100 Copenhagen, Denmark.
Department of Neurology, Herlev Gentofte Hospital, 2730 Herlev, Denmark.

Arne Møller (A)

Department of Nuclear Medicine and PET Center, Aarhus University Hospital, 8200 Aarhus, Denmark.
Institute of Clinical Medicine, Center of Functionally Integrative Neuroscience, 8000 Aarhus, Denmark.

Matilda Degn (M)

Pediatric Oncology Laboratory, Department of Pediatrics and Adolescent Medicine, University Hospital Rigshospitalet, 2100 Copenhagen, Denmark.

Kate L Lambertsen (KL)

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Department of Neurology, Odense University Hospital, 5000 Odense, Denmark.
Brain Research-Inter-Disciplinary Guided Excellence (BRIDGE), Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.
OPEN-Open Patient data Explorative Network, Department of Clinical Research, Odense University Hospital, University of Southern Denmark, 5000 Odense, Denmark.

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