Cardiac-specific overexpression of tumor necrosis factor-alpha causes lethal myocarditis in transgenic mice
- PMID: 9220311
- DOI: 10.1016/s1071-9164(97)90045-2
Cardiac-specific overexpression of tumor necrosis factor-alpha causes lethal myocarditis in transgenic mice
Abstract
Background: Tumor necrosis factor (TNF)-alpha, a proinflammatory cytokine with negative inotropic effects, can be detected in myocardium with end-stage heart failure, after endotoxin administration, and during transplant rejection. Various studies suggest that TNF-alpha participates in the pathogenesis of cardiac dysfunction. To test this hypothesis, transgenic mice were made that selectively overexpress TNF-alpha in cardiomyocytes.
Methods and results: A transgene construct was made containing the murine alpha-myosin heavy chain promoter and the coding sequence of murine TNF-alpha, followed by the simian virus 40 T-antigen intron and polyadenylation signals. Injection of this construct into fertilized eggs yielded three transgenic mice, all of which died spontaneously before the completion of weaning. Gross pathologic analysis of these mice demonstrated a decrease in body weight with markedly increased heart weight. Histologic examination of the heart revealed a substantial, diffuse lymphohistiocytic inflammatory infiltrate, associated with interstitial edema. Reverse transcriptase polymerase chain reaction showed that the transgene was expressed in the heart. Enzyme-linked immunosorbent assay demonstrated a substantial amount of TNF-alpha protein in the transgenic heart.
Conclusion: Overexpression of TNF-alpha in the heart leads to severe myocarditis and cardiomegaly. These results support the hypothesis that myocardial expression of TNF-alpha can contribute to the pathogenesis of cardiac dysfunction.
Similar articles
-
Dilated cardiomyopathy in transgenic mice with cardiac-specific overexpression of tumor necrosis factor-alpha.Circ Res. 1997 Oct;81(4):627-35. doi: 10.1161/01.res.81.4.627. Circ Res. 1997. PMID: 9314845
-
Targeted disruption of ICAM-1, P-selectin genes improves cardiac function and survival in TNF-alpha transgenic mice.Am J Physiol Heart Circ Physiol. 2001 Apr;280(4):H1464-71. doi: 10.1152/ajpheart.2001.280.4.H1464. Am J Physiol Heart Circ Physiol. 2001. PMID: 11247755
-
Cardiac failure in transgenic mice with myocardial expression of tumor necrosis factor-alpha.Circulation. 1998 Apr 14;97(14):1375-81. doi: 10.1161/01.cir.97.14.1375. Circulation. 1998. PMID: 9577949
-
Expression of tumor necrosis factor-alpha--converting enzyme and tumor necrosis factor-alpha in human myocarditis.J Am Coll Cardiol. 2000 Oct;36(4):1288-94. doi: 10.1016/s0735-1097(00)00827-5. J Am Coll Cardiol. 2000. PMID: 11028485
-
Overexpression of cardiac I-kappaBalpha prevents endotoxin-induced myocardial dysfunction.Am J Physiol Heart Circ Physiol. 2001 Mar;280(3):H962-8. doi: 10.1152/ajpheart.2001.280.3.H962. Am J Physiol Heart Circ Physiol. 2001. PMID: 11179036
Cited by
-
Cardiac Gene Expression Knockdown Using Small Inhibitory RNA-Loaded Microbubbles and Ultrasound.PLoS One. 2016 Jul 29;11(7):e0159751. doi: 10.1371/journal.pone.0159751. eCollection 2016. PLoS One. 2016. PMID: 27471848 Free PMC article.
-
Myocardial dysfunction in rheumatoid arthritis: epidemiology and pathogenesis.Arthritis Res Ther. 2005;7(5):195-207. doi: 10.1186/ar1814. Epub 2005 Aug 24. Arthritis Res Ther. 2005. PMID: 16207349 Free PMC article. Review.
-
Cardiovascular inflammation: RNA takes the lead.J Mol Cell Cardiol. 2019 Apr;129:247-256. doi: 10.1016/j.yjmcc.2019.03.012. Epub 2019 Mar 14. J Mol Cell Cardiol. 2019. PMID: 30880251 Free PMC article. Review.
-
Complexity of TNF-α Signaling in Heart Disease.J Clin Med. 2020 Oct 12;9(10):3267. doi: 10.3390/jcm9103267. J Clin Med. 2020. PMID: 33053859 Free PMC article. Review.
-
Chronic intermittent hypoxia exposure improves left ventricular contractility in transgenic mice with heart failure.J Appl Physiol (1985). 2012 Sep 1;113(5):791-8. doi: 10.1152/japplphysiol.00185.2012. Epub 2012 Jul 5. J Appl Physiol (1985). 2012. PMID: 22773770 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources