Eosinophils Induce Airway Smooth Muscle Cell Proliferation

被引:0
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作者
Rabih Halwani
Alejandro Vazquez-Tello
Yuki Sumi
Mary Angeline Pureza
Ahmed Bahammam
Hamdan Al-Jahdali
Abdelillah Soussi-Gounni
Bassam Mahboub
Saleh Al-Muhsen
Qutayba Hamid
机构
[1] King Saud University,Asthma Research Chair and Prince Naif Center for Immunology Research, College of Medicine
[2] McGill University,Meakins
[3] King Saud University for health sciences,Christie Laboratories
[4] University of Manitoba,Department of Medicine, Pulmonary Division
[5] University of Sharjah,ICU
[6] King Saud University,Department of Immunology
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关键词
Asthma; airway remodeling; airway smooth muscle (ASM); proliferation; eosinophils; extra cellular matrix (ECM); cysteinyl leukotrienes;
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摘要
Asthma is characterized by eosinophilic airway inflammation and remodeling of the airway wall. Features of airway remodeling include increased airway smooth muscle (ASM) mass. However, little is known about the interaction between inflammatory eosinophils and ASM cells. In this study, we investigated the effect of eosinophils on ASM cell proliferation. Eosinophils were isolated from peripheral blood of mild asthmatics and non-asthmatic subjects and co-cultured with human primary ASM cells. ASM proliferation was estimated using Ki-67 expression assay. The expression of extracellular matrix (ECM) mRNA in ASM cells was measured using quantitative real-time PCR. The role of eosinophil derived Cysteinyl Leukotrienes (CysLTs) in enhancing ASM proliferation was estimated by measuring the release of leukotrienes from eosinophils upon their direct contact with ASM cells using ELISA. This role was confirmed either by blocking eosinophil-ASM contact or co-culturing them in the presence of leukotrienes antagonist. ASM cells co-cultured with eosinophils, isolated from asthmatics, but not non-asthmatics, had a significantly higher rate of proliferation compared to controls. This increase in ASM proliferation was independent of their release of ECM proteins but dependent upon eosinophils release of CysLTs. Eosinophil-ASM cell to cell contact was required for CysLTs release. Preventing eosinophil contact with ASM cells using anti-adhesion molecules antibodies, or blocking the activity of eosinophil derived CysLTs using montelukast inhibited ASM proliferation. Our results indicated that eosinophils contribute to airway remodeling during asthma by enhancing ASM cell proliferation and hence increasing ASM mass. Direct contact of eosinophils with ASM cells triggers their release of CysLTs which enhance ASM proliferation. Eosinophils, and their binding to ASM cells, constitute a potential therapeutic target to interfere with the series of biological events leading to airway remodeling and Asthma.
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页码:595 / 604
页数:9
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