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Sex-related survival differences in murine cardiomyopathy are associated with differences in TNF-receptor expression
Toshiaki Kadokami, … , Carole S. Frye, Arthur M. Feldman
Toshiaki Kadokami, … , Carole S. Frye, Arthur M. Feldman
Published August 15, 2000
Citation Information: J Clin Invest. 2000;106(4):589-597. https://doi.org/10.1172/JCI9307.
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Article

Sex-related survival differences in murine cardiomyopathy are associated with differences in TNF-receptor expression

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Abstract

Epidemiological evidence suggests that the prognosis of heart failure in women is better than in men. In our murine model of dilated cardiomyopathy arising from cardiac-specific overexpression of TNF-α, the 6-month survival rate was significantly better in females than in males. Young female transgenic mice exhibited left ventricular wall thickening without dilatation, whereas age-matched male transgenic hearts were markedly dilated. Basal and isoproterenol-stimulated fractional shortening was preserved in female transgenic mice, but not in male transgenic mice. Myocardial expression of proinflammatory cytokines and the extent of myocardial infiltrates were similar in male and female transgenic mice. Myocardial expression of TNF-receptor mRNAs (type I and type II) was significantly higher in male mice in both transgenic and wild-type littermates, whereas sex-specific differences were not observed in either peripheral white blood cells or liver tissue. After TNF-α challenge, myocardial but not liver production of ceramide was significantly higher in male than in female mice. Thus, differential expression of myocardial TNF receptors may contribute to sex differences in the severity of congestive heart failure and mortality consequent to cardiac-specific overexpression of TNF-α.

Authors

Toshiaki Kadokami, Charles F. McTiernan, Toru Kubota, Carole S. Frye, Arthur M. Feldman

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Figure 4

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Cytokine-receptor expression in myocardium. Representative images (a) an...
Cytokine-receptor expression in myocardium. Representative images (a) and quantitative results of RNase protection assays for TNFR1 (b) and TNFR2 (c). Quantitative results are reported as the ratio of the pixel intensity of each protected probe normalized to that of the GAPDH probe included in each template set as an internal control, as described in Methods. TNF1.6 mice expressed significantly more TNF receptors. In addition, the transcript level of TNF receptors was significantly higher in males relative to females in both TNF1.6 and wild-type mice. Values are mean ± SD (n = 6). Y-axis values correspond to the signal intensity of the hybridized probe in pixels normalized to that of GAPDH. TG, TNF1.6 mice; WT, wild-type mice; M, male; F, female. AP < 0.001 vs. females of the same genotype. BP < 0.01 vs. wild-type of the same sex.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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