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
相关论文
共 37 条
[31]   Nitric oxide and T helper cell immunity [J].
van der Veen, RC .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2001, 1 (08) :1491-1500
[32]   Superoxide prevents nitric oxide-mediated suppression of helper T lymphocytes: Decreased autoimmune encephalomyelitis in nicotinamide adenine dinucleotide phosphate oxidase knockout mice [J].
van der Veen, RC ;
Dietlin, TA ;
Hofman, FM ;
Pen, L ;
Segal, BH ;
Holland, SM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :5177-5183
[33]   Both expansion of regulatory GRI+ CD11b+ myeloid cells and anergy of T lymphocytes participate in hyporesponsiveness of the lung-associated immune system during acute toxoplasmosis [J].
Voisin, MB ;
Buzoni-Gatel, D ;
Bout, D ;
Velge-Roussel, F .
INFECTION AND IMMUNITY, 2004, 72 (09) :5487-5492
[34]   Molecular mechanisms of high-dose antigen therapy in experimental autoimmune encephalomyelitis:: Rapid induction of Th1-type cytokines and inducible nitric oxide synthase [J].
Weishaupt, A ;
Jander, S ;
Brück, W ;
Kuhlmann, T ;
Stienekemeier, M ;
Hartung, T ;
Toyka, KV ;
Stoll, G ;
Gold, R .
JOURNAL OF IMMUNOLOGY, 2000, 165 (12) :7157-7163
[35]  
Willenborg DO, 1999, J IMMUNOL, V163, P5278
[36]   SIN-1, a nitric oxide donor, ameliorates experimental allergic encephalomyelitis in Lewis rats in the incipient phase: The importance of the time window [J].
Xu, LY ;
Yang, JS ;
Link, H ;
Xiao, BG .
JOURNAL OF IMMUNOLOGY, 2001, 166 (09) :5810-5816
[37]   Bone marrow-derived versus parenchymal sources of inducible nitric oxide synthase in experimental autoimmune encephalomyelitis [J].
Zehntner, SP ;
Bourbonniere, L ;
Hassan-Zahraee, M ;
Tran, E ;
Owens, T .
JOURNAL OF NEUROIMMUNOLOGY, 2004, 150 (1-2) :70-79