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European Respiratory Society, European Respiratory Journal, 3(47), p. 769-782, 2016

DOI: 10.1183/13993003.00437-2015

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Activin-A is overexpressed in severe asthma and is implicated in angiogenic processes

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Activin-A is a pleiotropic cytokine that regulates allergic inflammation. Its role in the regulation of angiogenesis, a key feature of airways remodelling in asthma, remains unexplored. Our objective was to investigate the expression of activin-A in asthma and its effects on angiogenesisin vitro.Expression of soluble/immunoreactive activin-A and its receptors was measured in serum, bronchoalveolar lavage fluid (BALF) and endobronchial biopsies from 16 healthy controls, 19 patients with mild/moderate asthma and 22 severely asthmatic patients.In vitroeffects of activin-A on baseline and vascular endothelial growth factor (VEGF)-induced human endothelial cell angiogenesis, signalling and cytokine release were compared with BALF concentrations of these cytokinesin vivo.Activin-A expression was significantly elevated in serum, BALF and bronchial tissue of the asthmatics, while expression of its protein receptors was reduced.In vitro, activin-A suppressed VEGF-induced endothelial cell proliferation and angiogenesis, inducing autocrine production of anti-angiogenic soluble VEGF receptor (R)1 and interleukin (IL)-18, while reducing production of pro-angiogenic VEGFR2 and IL-17. In parallel, BALF concentrations of soluble VEGFR1 and IL-18 were significantly reduced in severe asthmaticsin vivoand inversely correlated with angiogenesis.Activin-A is overexpressed and has anti-angiogenic effectsin vitrothat are not propagatedin vivo, where reduced basal expression of its receptors is observed particularly in severe asthma.