The location of splenic NKT cells favours their rapid activation by blood-borne antigen

被引:81
作者
Barral, Patricia [1 ,2 ]
Sanchez-Nino, Maria Dolores [1 ]
van Rooijen, Nico [3 ]
Cerundolo, Vincenzo [2 ]
Batista, Facundo D. [1 ]
机构
[1] London Res Inst, Lymphocyte Interact Lab, Canc Res UK, London WC2A 3LY, England
[2] John Radcliffe Hosp, MRC, Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DU, England
[3] Vrije Univ Amsterdam, Dept Mol Cell Biol, Fac Med, VUMC, Amsterdam, Netherlands
基金
英国惠康基金;
关键词
blood-borne antigen; marginal zone; NKT cells; KILLER T-CELLS; MARGINAL ZONE MACROPHAGES; B-CELLS; DENDRITIC CELLS; LIPID ANTIGENS; IN-SITU; DEPLETION; ENTRY; MOUSE; MECHANISM;
D O I
10.1038/emboj.2012.87
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural killer T (NKT) cells play an important role in mounting protective responses to blood-borne infections. However, though the spleen is the largest blood filter in the body, the distribution and dynamics of NKT cells within this organ are not well characterized. Here we show that the majority of NKT cells patrol around the marginal zone (MZ) and red pulp (RP) of the spleen. In response to lipid antigen, these NKT cells become arrested and rapidly produce cytokines, while the small proportion of NKT cells located in the white pulp (WP) exhibit limited activation. Importantly, disruption of the splenic MZ by chemical or genetic approaches results in a severe reduction in NKT cell activation indicating the need of cooperation between both MZ macrophages and dendritic cells for efficient NKT cell responses. Thus, the location of splenic NKT cells in the MZ and RP facilitates their access to blood-borne antigen and enables the rapid initiation of protective immune responses. The EMBO Journal (2012) 31, 2378-2390. doi: 10.1038/emboj.2012.87; Published online 13 April 2012
引用
收藏
页码:2378 / 2390
页数:13
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