Diurnal Differences in Immune Response in Brain, Blood and Spleen After Focal Cerebral Ischemia in Mice.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
12 2022
Historique:
pubmed: 3 11 2022
medline: 1 12 2022
entrez: 2 11 2022
Statut: ppublish

Résumé

The immune response to acute cerebral ischemia is a major factor in stroke pathobiology. Circadian biology modulates some aspects of immune response. The goal of this study is to compare key parameters of immune response during the active/awake phase versus inactive/sleep phase in a mouse model of transient focal cerebral ischemia. Mice were housed in normal or reversed light cycle rooms for 3 weeks, and then they were blindly subjected to transient focal cerebral ischemia. Flow cytometry was used to examine immune responses in blood, spleen, and brain at 3 days after ischemic onset. In blood, there were higher levels of circulating T cells in mice subjected to focal ischemia during zeitgeber time (ZT)1-3 (inactive or sleep phase) versus ZT13-15 mice (active or awake phase). In the spleen, organ weight and immune cell numbers were lower in ZT1-3 versus ZT13-15 mice. Consistent with these results, there was an increased infiltration of activated T cells into brain at ZT1-3 compared with ZT13-15. This proof-of-concept study indicates that there are significant diurnal effects on the immune response after focal cerebral ischemia in mice. Hence, therapeutic strategies focused on immune targets should be reassessed to account for the effects of diurnal rhythms and circadian biology in nocturnal rodent models of stroke.

Sections du résumé

BACKGROUND
The immune response to acute cerebral ischemia is a major factor in stroke pathobiology. Circadian biology modulates some aspects of immune response. The goal of this study is to compare key parameters of immune response during the active/awake phase versus inactive/sleep phase in a mouse model of transient focal cerebral ischemia.
METHODS
Mice were housed in normal or reversed light cycle rooms for 3 weeks, and then they were blindly subjected to transient focal cerebral ischemia. Flow cytometry was used to examine immune responses in blood, spleen, and brain at 3 days after ischemic onset.
RESULTS
In blood, there were higher levels of circulating T cells in mice subjected to focal ischemia during zeitgeber time (ZT)1-3 (inactive or sleep phase) versus ZT13-15 mice (active or awake phase). In the spleen, organ weight and immune cell numbers were lower in ZT1-3 versus ZT13-15 mice. Consistent with these results, there was an increased infiltration of activated T cells into brain at ZT1-3 compared with ZT13-15.
CONCLUSIONS
This proof-of-concept study indicates that there are significant diurnal effects on the immune response after focal cerebral ischemia in mice. Hence, therapeutic strategies focused on immune targets should be reassessed to account for the effects of diurnal rhythms and circadian biology in nocturnal rodent models of stroke.

Identifiants

pubmed: 36321457
doi: 10.1161/STROKEAHA.122.040547
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e507-e511

Auteurs

Elga Esposito (E)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

Fang Zhang (F)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

Ji-Hyun Park (JH)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

Emiri T Mandeville (ET)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

Wenlu Li (W)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

María Isabel Cuartero (MI)

Neurovascular Pathophysiology Group, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain (M.I.C., M.A.M.).

Ignacio Lizasoaín (I)

Unidad de Investigación Neurovascular, Department of Pharmacology, Faculty of Medicine, Universidad Complutense and Instituto de Investigación Hospital 12 de Octubre (i+12), Madrid, Spain (I.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

María A Moro (MA)

Neurovascular Pathophysiology Group, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain (M.I.C., M.A.M.).

Eng H Lo (EH)

Neuroprotection Research Laboratories, Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston (E.E., F.Z., J.H.P., E.T.M., W.L., E.H.L.).
Consortium International pour la Recherche Circadienne sur l'AVC (CIRCA) (E.E., F.Z., J.H.P., E.T.M., W.L., I.L., M.A.M., E.H.L.).

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