C-Type Lectin Receptors Dectin-3 and Dectin-2 Form a Heterodimeric Pattern-Recognition Receptor for Host Defense against Fungal Infection

被引:277
作者
Zhu, Le-Le [1 ]
Zhao, Xue-Qiang [2 ]
Jiang, Changying [2 ]
You, Yun [2 ]
Chen, Xiao-Ping [1 ]
Jiang, Yuan-Ying [3 ]
Jia, Xin-Ming [1 ]
Lin, Xin [2 ,4 ]
机构
[1] Tongji Univ, Sch Med, Dept Immunol, Shanghai 200092, Peoples R China
[2] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[3] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
[4] Univ Texas Houston, Grad Sch Biomed Sci, Canc Biol Program, Houston, TX 77030 USA
关键词
BETA-GLUCAN RECEPTOR; NF-KAPPA-B; CANDIDA-ALBICANS; INNATE IMMUNE; CELL-SURFACE; ACTIVATION; SUSCEPTIBILITY; ASSOCIATION; MACROPHAGES; NEUTROPHILS;
D O I
10.1016/j.immuni.2013.05.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
C-type lectin receptors (CLRs) play critical roles as pattern-recognition receptors (PRRs) for sensing Candida albicans infection, which can be life-threatening for immunocompromised individuals. Here we have shown that Dectin-3 (also called CLECSF8, MCL, or Clec4d), a previously uncharacterized CLR, recognized alpha-mannans on the surfaces of C. albicans hyphae and induced NF-kappa B activation. Mice with either blockade or genetically deleted Dectin-3 were highly susceptible to C. albicans infection. Dectin-3 constantly formed heterodimers with Dectin-2, a well-characterized CLR, for recognizing C. albicans hyphae. Compared to their respective homodimers, Dectin-3 and Dectin-2 heterodimers bound alpha-mannans more effectively, leading to potent inflammatory responses against fungal infections. Together, our study demonstrates that Dectin-3 forms a heterodimeric PRR with Dectin-2 for sensing fungal infection and suggests that different CLRs may form different hetero- and homodimers, which provide different sensitivity and diversity for host cells to detect various microbial infections.
引用
收藏
页码:324 / 334
页数:11
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