Cited by 141Immune Response and InflammationCardiac Fibrosis and RemodelingCardiac Ischemia and Reperfusion

Cardiomyocyte Toll-like receptor 4 is involved in heart dysfunction following septic shock or myocardial ischemia

Fallach, Reut, Shainberg, Asher, Avlas, Orna, Fainblut, Michael, Chepurko, Yelena, Porat, Eyal, Hochhauser, Edith·2010·Journal of Molecular and Cellular Cardiology

Abstract

Toll-like receptors are expressed in immune cells and cardiac muscle. We examined whether the cardiac Toll-like receptor 4 (TLR4) is involved in the acute myocardial dysfunction caused by septic shock and myocardial ischemia (MI). We used wild type mice (WT), TLR4 deficient (TLR4-ko) mice and chimeras that underwent myeloablative bone marrow transplantation to dissociate between TLR4 expression in the heart (TLR4-ko/WT) and the immunohematopoietic system (WT/TLR4-ko). Mice were injected with lipopolysaccharide (LPS) (septic shock model) or subjected to coronary artery ligation (MI model) and tested in vivo and ex vivo, for function, histopathology proinflammatory cytokine and TLR4 expression. WT mice challenged with LPS or MI displayed reduced cardiac function, increased myocardial levels of IL-1 beta and TNF-alpha and upregulation of mRNA encoding TLR4 prior to myocardial leukocyte infiltration. TLR4 deficient mice sustained significantly smaller infarctions as compared to control mice at comparable areas at risk. The cardiac function of TLR4-ko mice was not affected by LPS and demonstrated reduced suppression by MI compared to WT. Chimeras deficient in myocardial TLR4 were resistant to suppression induced by LPS and the heart function was less depressed, compared to the TLR4-ko, following MI in the acute phase (4h). In contrast, hearts of chimeras deficient in immunohematopoietic TLR4 expression were suppressed both by LPS and MI, exhibiting increased myocardial cytokine le…

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Crossref · 10.1016/j.yjmcc.2010.02.020

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  • The TLR4, caspase-1, and NLRP3 pathways are upregulated in patients, EAM, autoimmune CVB3 myocarditis, and CVB3-only models and increase IL-1β and IL-18 levels in the heart.

    “Another key pathway upregulated in patients, EAM, autoimmune CVB3 myocarditis, and CVB3only models is the TLR4, caspase-1, and NLRP3 pathways that increase IL-1 β and IL-18 levels in the heart. 124,146,152,156,161-164”

    From COVID-19, Myocarditis and Pericarditis (2023) · cites this paper as [164]

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Authors
Fallach, R., Shainberg, A., Avlas, O., Fainblut, M., Chepurko, Y., Porat, E., & Hochhauser, E.
Affiliations
  • Bar-Ilan University (IL)
  • Tel Aviv University (IL)
Venue
Journal of Molecular and Cellular Cardiology
Publisher
Elsevier BV
Published
2010-06
Volume
48
Issue
6
Pages
1236-1244
ISSN
0022-2828 (ISSN-L)
OpenAlex
W2051266478
Cited by
141
References
1
Citations by year
2026: 1 · 2025: 4 · 2024: 2 · 2023: 8 · 2022: 5 · 2021: 18 · 2020: 8 · 2019: 12 · 2018: 10 · 2017: 9 · 2016: 7 · 2015: 12 · 2014: 12 · 2013: 10 · 2012: 4
FWCI
4.40
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Molecular and Cellular Cardiology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Ministry of Health, State of Israel
  • Bar-Ilan University
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
Keywords
TLR4, cardiomyocytes, septic shock, myocardial ischemia, cardiac dysfunction, lipopolysaccharide, myocardial infarction, inflammatory cytokines, IL-1β, TNF-α, TLR4-deficient mice, chimeric mice
MeSH terms
Animals, Heart, Hemodynamics, Lipopolysaccharides, Male, Mice, Inbred C57BL, Myocardium, Shock, Septic, Tumor Necrosis Factor-alpha, Up-Regulation, Myocardial Ischemia, Mice, Knockout, Myocytes, Cardiac, Toll-Like Receptor 4, Mice, Interleukin-1beta

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