Journal
AMERICAN JOURNAL OF PATHOLOGY
Volume 171, Issue 1, Pages 315-325Publisher
ELSEVIER SCIENCE INC
DOI: 10.2353/ajpath.2007.061078
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- Wellcome Trust Funding Source: Medline
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Interleukin (IL)-6 acts via a receptor complex consisting of the cognate IL-6 receptor (IL-6R) or the soluble IL-6 receptor (sIL-6R) and glycoprotein 130 (gp130). Here, we investigated the role of these IL-6R components in hypertension and vascular hypertrophy in mice. Angiotensin (Ang) H (1.1 mg/kg/day) caused hypertension and cardiac/aortic hypertrophy in wildtype, but not IL-6(-/-), mice throughout 7 days. A recombinant dimeric soluble gp130 (sgp130Fc; 50 to 100 mu g, i.p.) blocked Ang H hypertension but not hypertrophy in wild-type mice. Cognate IL-6R was detected in aortic smooth muscle, but its levels and those of plasma sIL-6R were similar to 50% decreased in IL6(-/-) mice. Ang H infusion activated signal transducer and activator of transcription-3 in heart of WT and decreased Ang H receptor 1 (ATR1) expression in aorta. Both responses were unaffected by sgp130Fc and absent in IL-6(-/-) mice. In summary, we show that 11,6 trans-signaling is required for Ang II-dependent hypertension, but that hypertrophy, down-regulation of AT1R, and cardiac signal transducer and activator of transcription-3 activation are mediated via cognate IL-6R. These data show that IL-6 responses in a single disease context are governed by both modes of IL-6 signaling, with each pathway eliciting different outcomes. inhibition of IL-6 signaling is suggested as a potential therapy for hypertension and cardiac hypertrophy.
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