Sex differences in M2 polarization, chemokine and IL-4 receptors in monocytes and macrophages from asthmatics

被引:20
|
作者
Becerra-Diaz, Mireya [1 ]
Lerner, Andrew D. [1 ,2 ]
Yu, Diana H. [1 ,2 ]
Thiboutot, Jeffrey P. [1 ,2 ]
Liu, Mark C. [1 ,2 ]
Yarmus, Lonny B. [1 ,2 ]
Bose, Sonali [1 ,2 ]
Heller, Nicola M. [1 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pulm & Crit Care Med, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Allergy & Clin Immunol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
Asthma; Allergic lung inflammation; Sex differences; Monocytes; Alveolar macrophages; Hormones; IL-4; Chemokine; Cell recruitment;
D O I
10.1016/j.cellimm.2020.104252
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Allergic asthma affects more women than men. It is mediated partially by IL-4/IL-13-driven polarization of monocyte-derived macrophages in the lung. We tested whether sex differences in asthma are due to differential IL-4 responsiveness and/or chemokine receptor expression in monocytes and monocyte-derived macrophages from healthy and allergic asthmatic men and women. We found female cells expressed M2 genes more robustly following IL-4 stimulation than male cells, as did cells from asthmatics than those from healthy controls. This likely resulted from increased expression of gamma C, part of the type I IL-4 receptor, and reduced IL-4-induced SOCS1, a negative regulator of IL-4 signaling, in asthmatic compared to healthy macrophages. Monocytes from asthmatic women expressed more CX3CR1, which enhances macrophage survival. Our findings highlight how sex differences in IL-4 responsiveness and chemokine receptor expression may affect monocyte recruitment and macrophage polarization in asthma, potentially leading to new sex-specific therapies to manage the disease.
引用
收藏
页数:10
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