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Scavenger receptor-A functions in phagocytosis of E-coli by bone marrow dendritic cells
被引:33
作者:
Amiel, Eyal
Nicholson-Dykstra, Susan
Walters, Julie Jo
Higgs, Henry
Berwin, Brent
[1
]
机构:
[1] Dartmouth Med Sch, Dept Microbiol & Immunol, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Dept Biochem, Lebanon, NH 03756 USA
关键词:
dendritic cell;
bacteria;
phagocytosis;
trafficking;
scavenger receptor;
SR-A;
D O I:
10.1016/j.yexcr.2007.02.011
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Class-A scavenger receptors (SR-A) are cellular pattern recognition receptors that bind and traffic a variety of endogenous and microbial ligands. However, despite an emerging role for SR-A as a contributor to the innate immune system, little is known of the regulation or function of SR-A on dendritic cells (DCs). Here we show that SR-A expression is upregulated during murine DC differentiation and that SR-A expression levels correlate with the expression of the murine DC marker CD11c. Using bone marrow-derived DCs (BMDCs) from SR-A knockout (SR-A(-/-)) mice we investigated the contribution of SR-A to BMDC articulate phagocytosis. Functional analyses demonstrated that SR-A is a critical phagocytic receptor for BMDC internalization of the gram-negative bacteria E. coli. SR-A(-/-) BMDCs were impaired in their ability to phagocytose bacteria, and this deficit varied with the bacteria:BMDC cell ratio. Microscopic and biochemical analyses revealed that SR-A is broadly distributed on the surface of BMDCs and is not physically associated with lipid rafts. However, cholesterol depletion demonstrated dependence of SR-A-mediated phagocytosis upon lipid rafts. These data demonstrate a functional contribution for SR-A in the BMDC phagocytic pathway. (c) 2007 Elsevier Inc. All rights reserved.
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页码:1438 / 1448
页数:11
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