Saunders R, Sutcliffe A, Kaur D, Siddiqui S, Hollins F, Wardlaw A, Bradding P, Brightling C
Department of Infection, Immunity and Inflammation, Institute for Lung Health, University of Leicester, Leicester, UK.
Clin Exp Allergy. 2009 Nov;39(11):1684-92. doi: 10.1111/j.1365-2222.2009.03310.x. Epub 2009 Sep 7.
Chemokine receptors play an important role in cell migration and wound repair. In asthma, CCR3 and 7 are expressed by airway smooth muscle (ASM) and CCR7 has been implicated in the development of ASM hyperplasia. The expression profile of other chemokine receptors by ASM and their function needs to be further explored.
We sought to investigate ASM chemokine receptor expression and function in asthma.
ASM cells were derived from 17 subjects with asthma and 36 non-asthmatic controls. ASM chemokine receptor expression was assessed by flow cytometry and immunofluorescence. The function of chemokine receptors expressed by more than 10% of ASM cells was investigated by intracellular calcium measurements, chemotaxis, wound healing, proliferation and survival assays.
In addition to CCR3 and 7, CXCR1, 3 and 4 were highly expressed by ASM. These CXC chemokine receptors were functional with an increase in intracellular calcium following ligand activation and promotion of wound healing [CXCL10 (100 ng/mL) 34 +/- 2 cells/high-powered field (hpf) vs. control 29 +/- 1; P=0.03; n=8]. Spontaneous wound healing was inhibited by CXCR3 neutralizing antibody (mean difference 7 +/- 3 cells/hpf; P=0.03; n=3). CXC chemokine receptor activation did not modulate ASM chemotaxis, proliferation or survival. No differences in chemokine receptor expression or function were observed between ASM cells derived from asthmatic or non-asthmatic donors.
Our findings suggest that the chemokine receptors CXCR1, 3 and 4 modulate some aspects of ASM function but their importance in asthma is uncertain.
趋化因子受体在细胞迁移和伤口修复中发挥重要作用。在哮喘中,气道平滑肌(ASM)表达CCR3和CCR7,且CCR7与ASM增生的发展有关。ASM表达的其他趋化因子受体的表达谱及其功能有待进一步探索。
我们试图研究哮喘中ASM趋化因子受体的表达及功能。
ASM细胞来自17例哮喘患者和36例非哮喘对照者。通过流式细胞术和免疫荧光评估ASM趋化因子受体的表达。通过细胞内钙测量、趋化性、伤口愈合、增殖和存活测定,研究表达于超过10%ASM细胞的趋化因子受体的功能。
除CCR3和CCR7外,ASM还高表达CXCR1、CXCR3和CXCR4。这些CXC趋化因子受体具有功能,配体激活后细胞内钙增加,并促进伤口愈合[CXCL10(100 ng/mL)时为34±2个细胞/高倍视野(hpf),而对照组为29±1;P=0.03;n=8]。CXCR3中和抗体抑制自发伤口愈合(平均差异为7±3个细胞/hpf;P=0.03;n=3)。CXC趋化因子受体激活未调节ASM的趋化性、增殖或存活。哮喘或非哮喘供体来源的ASM细胞在趋化因子受体表达或功能上未观察到差异。
我们的研究结果表明,趋化因子受体CXCR1、CXCR3和CXCR4调节ASM功能的某些方面,但其在哮喘中的重要性尚不确定。