T cell expansion is regulated by activated Gr-1+ splenocytes

被引:8
作者
Dietlin, TA
Hofman, FM
Gilmore, W
Stohlman, SA
van der Veen, RC [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Neurol, Los Angeles, CA 90089 USA
[2] Univ So Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA USA
关键词
rodent; spleen and lymph nodes; nitric oxide;
D O I
10.1016/j.cellimm.2005.06.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CD4(+) T cell proliferation depends oil the balance between NO and extra-cellular superoxide (O-2(-)). By reducing NO bio-availability O-2(-) promotes splenic T cell proliferation and immune response intensity. Here, we show that spleen cells from naive mice produced neither NO nor O-2(-) during T cell activation, but Gr-1(+) splenocytes from primed mice regulated Ag-specific T cell expansion via Production of both molecules. Purified splenic Gr-1(+) cells included mostly granulocytes at various stages of maturation, its well as monocytes. Activation or recruitment of regulatory Gr-1(+) cells was dependent on immunization with CFA. Importantly, these regulatory cells were not detected in draining lymph nodes. These data suggest that innate Gr-1(+) splenic cells regulate adaptive immunity. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
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