Ischemic heart disease: Cellular and molecular immune contributions of the pericardium.

Immune Cells Inflammation Ischemic Heart Disease Pericardium

Journal

The international journal of biochemistry & cell biology
ISSN: 1878-5875
Titre abrégé: Int J Biochem Cell Biol
Pays: Netherlands
ID NLM: 9508482

Informations de publication

Date de publication:
11 2021
Historique:
received: 30 06 2021
revised: 30 08 2021
accepted: 07 09 2021
pubmed: 21 9 2021
medline: 17 12 2021
entrez: 20 9 2021
Statut: ppublish

Résumé

Ischemic heart disease promotes complex inflammatory and remodeling pathways which contribute to the development of chronic heart failure. Although blood-derived and local cardiac mediators have traditionally been linked with these processes, the pericardial space has more recently been noted as alternative contributor to the injury response in the heart. The pericardial space contains fluid rich in physiologically active mediators, and immunologically active adipose tissue, which are altered during myocardial infarction. Key immune cells in the pericardial fluid and adipose tissue have been identified which act as mediators for cell recruitment and function after myocardial infarction have been identified in experimental models. Here, we provide an overview of the current understanding of the inflammatory mechanisms of the pericardial space and their role in post-myocardial infarction remodeling and the potential for the use of the pericardial space as a delivery vehicle for treatments to modulate heart healing.

Identifiants

pubmed: 34543760
pii: S1357-2725(21)00157-6
doi: 10.1016/j.biocel.2021.106076
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

106076

Subventions

Organisme : CIHR
Pays : Canada

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Jameson A Dundas (JA)

Section of Cardiac Surgery, Department of Cardiac Sciences, Libin Cardiovascular Institute, Cumming School of Medicine, Calgary, Alberta, Canada.

Ali Fatehi Hassanabad (AF)

Section of Cardiac Surgery, Department of Cardiac Sciences, Libin Cardiovascular Institute, Cumming School of Medicine, Calgary, Alberta, Canada.

Anna N Zarzycki (AN)

Section of Cardiac Surgery, Department of Cardiac Sciences, Libin Cardiovascular Institute, Cumming School of Medicine, Calgary, Alberta, Canada.

Paul Wm Fedak (PW)

Section of Cardiac Surgery, Department of Cardiac Sciences, Libin Cardiovascular Institute, Cumming School of Medicine, Calgary, Alberta, Canada.

Justin F Deniset (JF)

Section of Cardiac Surgery, Department of Cardiac Sciences, Libin Cardiovascular Institute, Cumming School of Medicine, Calgary, Alberta, Canada; Department of Pharmacology and Physiology, University of Calgary, Calgary, Alberta, Canada. Electronic address: jdeniset@ucalgary.ca.

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Classifications MeSH