Synaptotagmin XI Regulates Phagocytosis and Cytokine Secretion in Macrophages

被引:44
作者
Duque, Guillermo Arango [1 ,2 ]
Fukuda, Mitsunori [3 ]
Descoteaux, Albert [1 ,2 ]
机构
[1] Univ Quebec, Inst Armand Frappier, Inst Natl Rech Sci, Laval, PQ H7V 1B7, Canada
[2] Ctr Host Parasite Interact, Laval, PQ H7V 1B7, Canada
[3] Tohoku Univ, Dept Dev Biol & Neurosci, Grad Sch Life Sci, Sendai, Miyagi 9808578, Japan
基金
加拿大健康研究院;
关键词
LEISHMANIA-DONOVANI AMASTIGOTES; TUMOR-NECROSIS-FACTOR; MEMBRANE; PHAGOSOME; EXOCYTOSIS; PROTEINS; BINDING; GENE; COMPARTMENT; INHIBITION;
D O I
10.4049/jimmunol.1202500
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Synaptotagmins (Syts) are a group of type I membrane proteins that regulate vesicle docking and fusion in processes such as exocytosis and phagocytosis. All Syts possess a single transmembrane domain, and two conserved tandem Ca2+-binding C2 domains. However, Syts IV and XI possess a conserved serine in their C2A domain that precludes these Syts from binding Ca2+ and phospholipids, and from mediating vesicle fusion. Given the importance of vesicular trafficking in macrophages, we investigated the role of Syt XI in cytokine secretion and phagocytosis. We demonstrated that Syt XI is expressed in murine macrophages, localized in recycling endosomes, lysosomes, and recruited to phagosomes. Syt XI had a direct effect on phagocytosis and on the secretion of TNF and IL-6. Whereas small interfering RNA-mediated knockdown of Syt XI potentiated secretion of these cytokines and particle uptake, overexpression of an Syt XI construct suppressed these processes. In addition, Syt XI knockdown led to decreased recruitment of gp91(phox) and lysosomal-associated membrane protein-1 to phagosomes, suggesting attenuated microbicidal activity. Remarkably, knockdown of Syt XI ensued in enhanced bacterial survival. Our data reveal a novel role for Syt XI as a regulator of cytokine secretion, particle uptake, and macrophage microbicidal activity. The Journal of Immunology, 2013, 190: 1737-1745.
引用
收藏
页码:1737 / 1745
页数:9
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