New Insights of CCR7 Signaling in Dendritic Cell Migration and Inflammatory Diseases

被引:52
作者
Hong, Wenxiang [1 ]
Yang, Bo [1 ]
He, Qiaojun [1 ,2 ,3 ]
Wang, Jiajia [1 ]
Weng, Qinjie [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, Ctr Drug Safety Evaluat & Res, Zhejiang Prov Key Lab Anticanc Drug Res, Hangzhou, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Hangzhou, Peoples R China
[3] Westlake Lab Life Sci & Biomed, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
CCR7; dendritic cells; migration; regulatory network; immunotherapy; UP-REGULATES CCR7; NF-KAPPA-B; LYMPH-NODES; T-CELLS; ENDOTHELIAL-CELLS; KINASE PATHWAY; MOUSE MODEL; EXPRESSION; TRAFFICKING; ACTIVATION;
D O I
10.3389/fphar.2022.841687
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CCR7, collaborated with its ligands CCL19 and CCL21, controls extensive migratory events in the immune system. CCR7-bearing dendritic cells can swarm into T-cell zones in lymph nodes, initiating the antigen presentation and T-cell response. Abnormal expression of CCR7 in dendritic cells will cause a series of inflammatory diseases due to the chaotic dendritic cell trafficking. In this review, we take an in-depth look at the structural-functional domains of CCR7 and CCR7-bearing dendritic cell trajectory to lymph nodes. Then, we summarize the regulatory network of CCR7, including transcriptional regulation, translational and posttranslational regulation, internalization, desensitization, and recycling. Furthermore, the potential strategies of targeting the CCR7 network to regulate dendritic cell migration and to deal with inflammatory diseases are integrated, which not only emphasizes the possibility of CCR7 to be a potential target of immunotherapy but also has an implication on the homing of dendritic cells to benefit inflammatory diseases.
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页数:14
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