Characterising the Mechanism of Airway Smooth Muscle ?2 Adrenoceptor Desensitization by Rhinovirus Infected Bronchial Epithelial Cells.
PLoS One. 2013;8(2):e56058
Authors: Van Ly D, Faiz A, Jenkins C, Crossett B, Black JL, McParland B, Burgess JK, Oliver BG
Abstract
Rhinovirus (RV) infections account for approximately two thirds of all virus-induced asthma exacerbations and often result in an impaired response to ? agonist therapy. Using an model of RV infection, we investigated the mechanisms underlying RV-induced ? adrenoceptor desensitization in primary human airway smooth muscle cells (ASMC). RV infection of primary human bronchial epithelial cells (HBEC) for 24 hours produced conditioned medium that caused ? adrenoceptor desensitization on ASMCs without an effect on ASMCs viability. Less than 3 kDa size fractionation together with trypsin digestion of RV-induced conditioned medium did not prevent ? adrenoceptor desensitization, suggesting it could potentially be mediated by a small peptide or lipid. RV infection of BECs, ASMCs and fibroblasts produced prostaglandins, of which PGE, PGF and PGI had the ability to cause ? adrenoceptor desensitization on ASMCs. RV-induced conditioned medium from HBECs depleted of PGE did not prevent ASMC ? adrenoceptor desensitization; however this medium induced PGE from ASMCs, suggesting that autocrine prostaglandin production may be responsible. Using inhibitors of cyclooxygenase and prostaglandin receptor antagonists, we found that ? adrenoceptor desensitization was mediated through ASMC derived COX-2 induced prostaglandins. Since ASMC prostaglandin production is unlikely to be caused by RV-induced epithelial derived proteins or lipids we next investigated activation of toll-like receptors (TLR) by viral RNA. The combination of TLR agonists poly I:C and imiquimod induced PGE and ? adrenoceptor desensitization on ASMC as did the RNA extracted from RV-induced conditioned medium. Viral RNA but not epithelial RNA caused ? adrenoceptor desensitization confirming that viral RNA and not endogenous human RNA was responsible. It was deduced that the mechanism by which ? adrenoceptor desensitization occurs was by pattern recognition receptor activation of COX-2 induced prostaglandins.
PMID: 23457497 [PubMed - in process]
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