Human Lung Mast Cell Products Regulate Airway Smooth Muscle CXCL10 Levels. (6th February 2014)

• Record Type: Journal Article
• Authors: Alkhouri, H.; Cha, V.; Tong, K.; Moir, L. M.; Armour, C. L.; Hughes, J. M.
• Other Names: Berger William E. Academic Editor.
• Is Part Of: Journal of allergy. Volume 2014(2014)
• Publication Date: 2014-02-06
• Subjects: Allergy -- Periodicals; Immunologic diseases -- Periodicals; Allergy and Immunology; Hypersensitivity; Immune System Diseases; Allergy; Immunologic diseases; Electronic journals; Periodical; Periodicals; 616.97
• DOI: 10.1155/2014/875105
• Languages: English
• ISSNs: 1687-9783

Abstract

Abstract : In asthma, the airway smooth muscle (ASM) produces CXCL10 which may attract CXCR3 + mast/T cells to it. Our aim was to investigate the effects of mast cell products on ASM cell CXCL10 production. ASM cells from people with and without asthma were stimulated with IL-1 β, TNF- α, and/or IFN γ and treated with histamine (1–100 μ M) ± chlorpheniramine (H1R antagonist; 1 μ M) or ranitidine (H2R antagonist; 50 μ M) or tryptase (1 nM) ± leupeptin (serine protease inhibitor; 50 μ M), heat-inactivated tryptase, or vehicle for 4 h or 24 h. Human lung mast cells (MC) were isolated and activated with IgE/anti-IgE and supernatants were collected after 2 h or 24 h. The supernatants were added to ASM cells for 48 h and ASM cell CXCL10 production detected using ELISA (protein) and real-time PCR (mRNA). Histamine reduced IL-1 β /TNF- α -induced CXCL10 protein, but not mRNA, levels independent of H1 and H2 receptor activation, whereas tryptase and MC 2 h supernatants reduced all cytokine-induced CXCL10. Tryptase also reduced CXCL10 levels in a cell-free system. Leupeptin inhibited the effects of tryptase and MC 2 h supernatants. MC 24 h supernatants contained TNF- α and amplified IFN γ -induced ASM cell CXCL10 production. This is the first evidence that MC can regulate ASM cell CXCL10 production and its degradation. Thus MC may regulate airway myositis in asthma.