Visualization of T Cell-Regulated Monocyte Clusters Mediating Keratinocyte Death in Acquired Cutaneous Immunity

被引:16
作者
Liu, Zheng [1 ,2 ]
Yang, Fei [1 ,2 ]
Zheng, Hao [1 ,2 ]
Fan, Zhan [1 ,2 ]
Qiao, Sha [1 ,2 ]
Liu, Lei [1 ,2 ]
Tao, Juan [3 ]
Luo, Qingming [1 ,2 ]
Zhang, Zhihong [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Britton Chance Ctr Biomed Photon, Wuhan, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Engn Sci, Collaborat Innovat Ctr Biomed Engn, Key Lab Biomed Photon,Minist Educ, Wuhan, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Dermatol, Wuhan, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
ALLERGIC CONTACT-DERMATITIS; DENDRITIC CELLS; IN-VIVO; APOPTOSIS; MIGRATION; PROTEIN; SKIN; INFLAMMATION; RECRUITMENT; ACTIVATION;
D O I
10.1016/j.jid.2018.01.018
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
It remains unclear how monocytes are mobilized to amplify inflammatory reactions in T cell-mediated adaptive immunity. Here, we investigate dynamic cellular events in the cascade of inflammatory responses through intravital imaging of a multicolor-labeled murine contact hypersensitivity model. We found that monocytes formed clusters around hair follicles in the contact hypersensitivity model. In this process, effector T cells encountered dendritic cells under regions of monocyte clusters and secreted IFN-gamma, which mobilizes CCR2-dependent monocyte interstitial migration and CXCR2-dependent monocyte cluster formation. We showed that hair follicles shaped the inflammatory microenvironment for communication among the monocytes, keratinocytes, and effector T cells. After disrupting the T cell-mobilized monocyte clusters through CXCR2 antagonization, monocyte activation and keratinocyte apoptosis were significantly inhibited. Our study provides a new perspective on effector T cell-regulated monocyte behavior, which amplifies the inflammatory reaction in acquired cutaneous immunity.
引用
收藏
页码:1328 / 1337
页数:10
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