Literature DB >> 28043025

NF-κB activation is cell type-specific in the heart.

Efraín E Rivera-Serrano1, Barbara Sherry2.   

Abstract

Viral myocarditis is common and can progress to cardiac failure. Cardiac cell pro-inflammatory responses are critical for viral clearance, however sustained inflammatory responses contribute to cardiac damage. The transcription factor NF-κB regulates expression of many pro-inflammatory cytokines, but basal and induced activation of NF-κB in different cardiac cell types have not been compared. Here, we used primary cultures of cardiac myocytes and cardiac fibroblasts to identify cardiac cell type-specific events. We show that while viral infection readily stimulates activation of NF-κB in cardiac fibroblasts, cardiac myocytes are largely recalcitrant to activation of NF-κB. Moreover, we show that cardiac myocyte subpopulations differ in their NF-κB subcellular localization and identify the cis-Golgi as a cardiac myocyte-specific host compartment. Together, results indicate that NF-κB-dependent signaling in the heart is cardiac cell type-specific, likely reflecting mechanisms that have evolved to balance responses that can be either protective or damaging to the heart.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cardiac fibroblast; Cardiac myocyte; Cardiomyocyte; Golgi; Heart; Myocarditis; NF-κB; Reovirus

Mesh:

Substances:

Year:  2016        PMID: 28043025      PMCID: PMC5276732          DOI: 10.1016/j.virol.2016.12.022

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  66 in total

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8.  Crosstalk between the type 1 interferon and nuclear factor kappa B pathways confers resistance to a lethal virus infection.

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6.  Cytokine-Mediated Alterations of Human Cardiac Fibroblast's Secretome.

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7.  Effects of Long Noncoding RNA HOTAIR Targeting miR-138 on Inflammatory Response and Oxidative Stress in Rat Cardiomyocytes Induced by Hypoxia and Reoxygenation.

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Review 10.  Mechanisms and Potential Treatment Options of Heart Failure in Patients With Multiple Myeloma.

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