Hippocampal NG2+ pericytes in chronically stressed rats and depressed patients: a quantitative study.


Journal

Stress (Amsterdam, Netherlands)
ISSN: 1607-8888
Titre abrégé: Stress
Pays: England
ID NLM: 9617529

Informations de publication

Date de publication:
05 2021
Historique:
pubmed: 18 6 2020
medline: 28 5 2021
entrez: 18 6 2020
Statut: ppublish

Résumé

The suggested link between major depression disorder (MDD) and blood-brain barrier (BBB) alterations supports an impact on the neurovascular unit in this disease condition. Here we investigate how pericytes, a major component in the neurovascular unit, respond to stress, stress hormones, proinflammatory cytokine and depression. Hippocampal sections of chronic unpredictable stressed (CMS) rats, MDD patients and respective controls were immuno-stained against NG2, where the number of NG2+ pericytes in the molecular layer was counted. Proliferation of cultured pericytes after treatment with cortisol and IL-1β was analyzed using radioactive-labeled thymidine. The number of NG2+ pericytes was significantly higher in CMS animals than controls. Higher number of NG2+ pericytes was also detected in MDD patients, but the increase did not reach significance. IL-1β, but not cortisol, induced a significant increase in proliferation of cultured pericytes. Our results indicate that exposure to stressful conditions affects the hippocampal pericyte population. These findings add to our knowledge about the impact of stress on the neurovascular unit, which might be relevant for understanding the alterations in BBB found in MDD patients.

Identifiants

pubmed: 32546032
doi: 10.1080/10253890.2020.1781083
doi:

Substances chimiques

Cytokines 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

353-358

Auteurs

Giulia Treccani (G)

Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Institute for Microscopic Anatomy and Neurobiology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Department of Clinical Sciences Malmö, Clinical Memory Research Unit, Lund University, Malmö, Sweden.

Anna-Lena Schlegelmilch (AL)

Department of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Nina Schultz (N)

Department of Clinical Sciences Malmö, Clinical Memory Research Unit, Lund University, Malmö, Sweden.

David P Herzog (DP)

Department of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Joao M Bessa (JM)

Life and Health Sciences Research Institute (ICVS), Medical School, University of Minho, Braga, Portugal.
ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal.

Ioannis Sotiropoulos (I)

Life and Health Sciences Research Institute (ICVS), Medical School, University of Minho, Braga, Portugal.
ICVS/3B's - PT Government Associate Laboratory, Braga, Guimarães, Portugal.

Marianne B Müller (MB)

Department of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.
Institute for Microscopic Anatomy and Neurobiology, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Malin Wennström (M)

Department of Clinical Sciences Malmö, Clinical Memory Research Unit, Lund University, Malmö, Sweden.

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