Differential impact of L-arginine deprivation on the activation and effector functions of T cells and macrophages

被引:71
作者
Choi, B. -S. [1 ]
Martinez-Falero, I. Clara [1 ]
Corset, C. [1 ]
Munder, M. [2 ]
Modolell, M. [3 ]
Mueller, I. [1 ]
Kropf, P. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Immunol, Fac Med, London W2 1PG, England
[2] Univ Heidelberg Hosp, Dept Hematol Oncol & Rheumatol, Heidelberg, Germany
[3] Max Planck Inst Immunobiol, Dept Cellular Immunol, D-7800 Freiburg, Germany
基金
英国惠康基金;
关键词
arginase; immune regulation; t cell hyporesponsiveness; iNOS; cytokine; chemokine; NITRIC-OXIDE SYNTHASE; MARROW-DERIVED MACROPHAGES; MYELOID SUPPRESSOR-CELLS; AMINO-ACID TRANSPORTERS; ARGINASE ACTIVITY; LEISHMANIA-MAJOR; ALTERNATIVE ACTIVATION; TRANSLATIONAL CONTROL; MURINE MACROPHAGES; MONONUCLEAR-CELLS;
D O I
10.1189/jlb.0508310
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The metabolism of the amino acid L-arginine is emerging as a crucial mechanism for the regulation of immune responses. Here, we characterized the impact of L-arginine deprivation on T cell and macrophage (M Phi) effector functions: We show that whereas L-arginine is required unconditionally for T cell activation, M Phi can up-regulate activation markers and produce cytokines and chemokines in the absence of L-arginine. Furthermore, we show that L-arginine deprivation does not affect the capacity of activated M Phi to up-regulate L-arginine-metabolizing enzymes such as inducible NO synthase and arginase 1. Thus, our results show that to exert their effector functions, T cells and M Phi have different requirements for L-arginine. J. Leukoc. Biol. 85: 268-277; 2009.
引用
收藏
页码:268 / 277
页数:10
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