Guidelines for evaluating myocardial cell death.


Journal

American journal of physiology. Heart and circulatory physiology
ISSN: 1522-1539
Titre abrégé: Am J Physiol Heart Circ Physiol
Pays: United States
ID NLM: 100901228

Informations de publication

Date de publication:
01 11 2019
Historique:
pubmed: 17 8 2019
medline: 9 4 2020
entrez: 17 8 2019
Statut: ppublish

Résumé

Cell death is a fundamental process in cardiac pathologies. Recent studies have revealed multiple forms of cell death, and several of them have been demonstrated to underlie adverse cardiac remodeling and heart failure. With the expansion in the area of myocardial cell death and increasing concerns over rigor and reproducibility, it is important and timely to set a guideline for the best practices of evaluating myocardial cell death. There are six major forms of regulated cell death observed in cardiac pathologies, namely apoptosis, necroptosis, mitochondrial-mediated necrosis, pyroptosis, ferroptosis, and autophagic cell death. In this article, we describe the best methods to identify, measure, and evaluate these modes of myocardial cell death. In addition, we discuss the limitations of currently practiced myocardial cell death mechanisms.

Identifiants

pubmed: 31418596
doi: 10.1152/ajpheart.00259.2019
pmc: PMC6879915
doi:

Substances chimiques

Biomarkers 0
Intracellular Signaling Peptides and Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review Webcast

Langues

eng

Sous-ensembles de citation

IM

Pagination

H891-H922

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL113281
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002649
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM113134
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL136816
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL116205
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

Paras K Mishra (PK)

Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska.

Adriana Adameova (A)

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University of Bratislava, Bratislava, Slovakia.

Joseph A Hill (JA)

Departments of Medicine (Cardiology) and Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas.

Christopher P Baines (CP)

Department of Biomedical Sciences, Dalton Cardiovascular Research Center, University of Missouri-Columbia, Columbia, Missouri.

Peter M Kang (PM)

Cardiovascular Division, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

James M Downey (JM)

Department of Physiology and Cell Biology, College of Medicine, University of South Alabama, Mobile, Alabama.

Jagat Narula (J)

Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Hospital, New York, New York.

Masafumi Takahashi (M)

Division of Inflammation Research, Center of Molecular Medicine, Jichi Medical University, Tochigi, Japan.

Antonio Abbate (A)

Virginia Commonwealth University, Pauley Heart Center, Richmond, Virginia.

Hande C Piristine (HC)

Department of Medicine (Cardiology), University of Texas Southwestern Medical Center, Dallas, Texas.

Sumit Kar (S)

Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska.

Shi Su (S)

Cardiovascular Division, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Jason K Higa (JK)

Department of Anatomy, Biochemistry, and Physiology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii.

Nicholas K Kawasaki (NK)

Department of Anatomy, Biochemistry, and Physiology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii.

Takashi Matsui (T)

Department of Anatomy, Biochemistry, and Physiology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii.

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Classifications MeSH