Eosinophil-derived chemokine (hCCL15/23, mCCL6) interacts with CCR1 to promote eosinophilic airway inflammation

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作者
Xufei Du
Fei Li
Chao Zhang
Na Li
Huaqiong Huang
Zhehua Shao
Min Zhang
Xueqin Zhan
Yicheng He
Zhenyu Ju
Wen Li
Zhihua Chen
Songmin Ying
Huahao Shen
机构
[1] the Second Affiliated Hospital of Zhejiang University School of Medicine,Key Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine
[2] Zhejiang University School of Medicine,Department of Anatomy
[3] Jinan University,Key Laboratory of Regenerative Medicine of Ministry of Education, Institute of Aging and Regenerative Medicine
[4] Zhejiang University School of Medicine,International Institutes of Medicine
[5] Zhejiang University School of Medicine,Department of Pharmacology
[6] State Key Lab of Respiratory Disease,undefined
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摘要
Eosinophils are terminally differentiated cells derived from hematopoietic stem cells (HSCs) in the bone marrow. Several studies have confirmed the effective roles of eosinophils in asthmatic airway pathogenesis. However, their regulatory functions have not been well elucidated. Here, increased C-C chemokine ligand 6 (CCL6) in asthmatic mice and the human orthologs CCL15 and CCL23 that are highly expressed in asthma patients are described, which are mainly derived from eosinophils. Using Ccl6 knockout mice, further studies revealed CCL6-dependent allergic airway inflammation and committed eosinophilia in the bone marrow following ovalbumin (OVA) challenge and identified a CCL6-CCR1 regulatory axis in hematopoietic stem cells (HSCs). Eosinophil differentiation and airway inflammation were remarkably decreased by the specific CCR1 antagonist BX471. Thus, the study identifies that the CCL6-CCR1 axis is involved in the crosstalk between eosinophils and HSCs during the development of allergic airway inflammation, which also reveals a potential therapeutic strategy for targeting G protein-coupled receptors (GPCRs) for future clinical treatment of asthma.
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