» Articles » PMID: 7635940

Tumor Necrosis Factor-alpha Gene and Protein Expression in Adult Feline Myocardium After Endotoxin Administration

Overview
Journal J Clin Invest
Specialty General Medicine
Date 1995 Aug 1
PMID 7635940
Citations 79
Authors
Affiliations
Soon will be listed here.
Abstract

TNF alpha mRNA and protein biosynthesis were examined in the adult feline heart after stimulation with endotoxin. When freshly isolated hearts were stimulated with endotoxin in vitro, de novo TNF alpha mRNA expression occurred within 30 min, and TNF alpha protein production was detected within 60-75 min; however, TNF alpha mRNA and protein production were not detected in diluent-treated hearts. Immunohistochemical studies localized TNF alpha to endothelial cells, smooth muscle cells, and cardiac myocytes in the endotoxin-treated hearts, whereas TNF alpha immunostaining was absent in the diluent-treated hearts. To determine whether the cardiac myocyte was a source for TNF alpha production, two studies were performed. First, in situ hybridization studies, using highly specific biotinylated probes, demonstrated TNF alpha mRNA in cardiac myocytes from endotoxin-stimulated hearts; in contrast, TNF alpha mRNA was not expressed in myocytes from diluent-treated hearts. Second, TNF alpha protein production was observed when cultured cardiac myocytes were stimulated with endotoxin, whereas TNF alpha protein production was not detected in the diluent-treated cells. The functional significance of the intramyocardial production of TNF alpha was determined by examining cell motion in isolated cardiac myocytes treated with superfusates from endotoxin- and diluent-stimulated hearts. These studies showed that cell motion was depressed in myocytes treated with superfusates from the endotoxin-treated hearts, but was normal with the superfusates from the diluent-treated hearts; moreover, the negative inotropic effects of the superfusates from the endotoxin-treated hearts could be abrogated completely by pretreatment with an anti-TNF alpha antibody. Finally, endotoxin stimulation was also shown to result in the intramyocardial production of TNF alpha mRNA and protein in vivo. Thus, this study shows for the first time that the adult mammalian myocardium synthesizes biologically active TNF alpha.

Citing Articles

Septic Cardiomyopathy.

Lukic I, Mihic D, Canecki Varzic S, Relatic K, Zibar L, Loinjak D Rev Cardiovasc Med. 2024; 25(1):23.

PMID: 39077653 PMC: 11262393. DOI: 10.31083/j.rcm2501023.


Research Advances in Targeted Therapy for Heart Failure.

Miao L, Liu Y Rev Cardiovasc Med. 2024; 24(10):276.

PMID: 39077559 PMC: 11262442. DOI: 10.31083/j.rcm2410276.


Strategies to attenuate maladaptive inflammatory response associated with cardiopulmonary bypass.

Banerjee D, Feng J, Sellke F Front Surg. 2024; 11:1224068.

PMID: 39022594 PMC: 11251955. DOI: 10.3389/fsurg.2024.1224068.


The secretome as a biomarker and functional agent in heart failure.

Nyarko O, Sucharov C J Cardiovasc Aging. 2023; 3(3).

PMID: 37484982 PMC: 10361342. DOI: 10.20517/jca.2023.15.


Intermittent Short-Duration Re-oxygenation Attenuates Cardiac Changes in Response to Hypoxia: Histological, Ultrastructural and Oxidant/Antioxidant Parameters.

Shati A, Zaki M, Alqahtani Y, Haidara M, Alshehri M, Dawood A Br J Biomed Sci. 2022; 79:10150.

PMID: 35996511 PMC: 9302540. DOI: 10.3389/bjbs.2022.10150.


References
1.
Tovey M . Expression of the genes of interferons and other cytokines in normal and diseased tissues of man. Experientia. 1989; 45(6):526-35. DOI: 10.1007/BF01990502. View

2.
Iezzoni J, Kang J, Bucana C, Reed J, Brigati D . Rapid colorimetric detection of epidermal growth factor receptor mRNA by in situ hybridization. J Clin Lab Anal. 1993; 7(5):247-51. DOI: 10.1002/jcla.1860070502. View

3.
Yokoyama T, Vaca L, Rossen R, Durante W, Hazarika P, Mann D . Cellular basis for the negative inotropic effects of tumor necrosis factor-alpha in the adult mammalian heart. J Clin Invest. 1993; 92(5):2303-12. PMC: 288411. DOI: 10.1172/JCI116834. View

4.
Lange L, Schreiner G . Immune mechanisms of cardiac disease. N Engl J Med. 1994; 330(16):1129-35. DOI: 10.1056/NEJM199404213301607. View

5.
Huang E, Morgan C, Sedmak D, Ferguson R, Orosz C . Alloantigenicity of human endothelial cells. IV. Derivation, characterization, and utilization of gonadal vein endothelia to control endothelial alloantigenicity during lymphocyte-endothelial interactions. Transplantation. 1994; 57(5):703-11. View