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Dectin-1 uses novel mechanisms for yeast phagocytosis in macrophages
被引:339
作者:
Herre, J
Marshall, ASJ
Caron, E
Edwards, AD
Williams, DL
Schweighoffer, E
Tybulewicz, V
Sousa, CRE
Gordon, S
[1
]
Brown, GD
机构:
[1] Univ Cape Town, Inst Infect Dis & Mol Med, ZA-7925 Rondebosch, South Africa
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[3] Univ London Imperial Coll Sci Technol & Med, Ctr Mol Microbiol & Infect, London, England
[4] Univ London Imperial Coll Sci Technol & Med, Dept Biol Sci, London, England
[5] Canc Res United Kingdom, Immunobiol Lab, London, England
[6] E Tennessee State Univ, James H Quillen Coll Med, Dept Surg, Johnson City, TN 37614 USA
[7] Natl Inst Med Res, London NW7 1AA, England
来源:
关键词:
D O I:
10.1182/blood-2004-03-1140
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The phagocytosis of pathogens is a critical event in host defense, not only for clearance of the invading microorganism, but also for the subsequent immune response. We have examined Dectin-1, a proinflammatory nonopsonic receptor for beta-glucans, and show that it mediates the internalization of P-glucan-bearing ligands, including yeast particles. Although requiring tyrosine phosphorylation and the cytoplasmic immunoreceptor tyrosine-based activation motif (ITAM)-like motif, uptake mediated by Dectin-1 was different from any previously reported phagocytic receptor and was not dependent on Syk-kinase in macrophages. Furthermore, intracellular trafficking of this receptor was influenced by the nature of the P-glucan ligand, which has significance for the biologic activity of these immunomodulatory carbohydrates. (C) 2004 by The American Society of Hematology.
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页码:4038 / 4045
页数:8
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