Arginase I is constitutively expressed in human granulocytes and participates in fungicidal activity

被引:270
作者
Munder, M
Mollinedo, F
Calafat, J
Canchado, J
Gil-Lamaignere, C
Fuentes, JM
Luckner, C
Doschko, G
Soler, G
Eichmann, K
Müller, FM
Ho, AD
Goerner, M
Modolell, M
机构
[1] Univ Heidelberg Hosp, Dept Hematol Oncol & Rheumatol, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Clin Cooperat Unit, D-6900 Heidelberg, Germany
[3] Heidelberg Univ, Inst Immunol, Heidelberg, Germany
[4] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, Ctr Invest Canc, E-37008 Salamanca, Spain
[5] Netherlands Canc Inst, Div Cell Biol, Amsterdam, Netherlands
[6] Heidelberg Univ, Childrens Hosp, Dept Pediat 3, Sect Pediat Pulm & Infect Dis, D-6900 Heidelberg, Germany
[7] Univ Extremadura, Dept Bioquim & Biol Mol, EU Enfermeria & TO, Caceres, Spain
[8] Univ Extremadura, Fac Vet, Dept Bioquim & Biol Mol, Caceres, Spain
[9] Max Planck Inst Immunobiol, Dept Cellular, D-7800 Freiburg, Germany
关键词
D O I
10.1182/blood-2004-07-2521
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The balance of arginine metabolism via nitric oxide synthase (NOS) or arginase is an important determinant of the inflammatory response of murine macrophages and dendritic cells. Here we analyzed the expression of the isoform arginase I in human myeloid cells. Using healthy donors and patients with arginase I deficiency, we found that in human leukocytes arginase I is constitutively expressed only in granulocytes and is not modulated by a variety of proinflammatory and anti-inflammatory stimuli in vitro. We demonstrate that arginase I is localized in azurophil granules of neutrophils and constitutes a novel antimicrobial effector pathway, likely through arginine depletion in the phagolysosome. Our findings demonstrate important differences between murine and human leukocytes with respect to regulation and function of arginine metabolism via arginase. (c) 2005 by The American Society of Hematology
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收藏
页码:2549 / 2556
页数:8
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