Peroxiredoxin II is essential for sustaining life span of erythrocytes in mice

被引:321
作者
Lee, TH
Kim, SU
Yu, SL
Kim, SH
Park, DS
Moon, HB
Dho, SH
Kwon, KS
Kwon, HJ
Han, YH
Jeong, S
Kang, SW
Shin, HS
Lee, KK
Rhee, SG
Yu, DY [1 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Lab Dev & Differentiat, Funct Proteom Lab, Taejon 305333, South Korea
[2] Wonkwang Univ, Sch Med, Dept Pathol, Iksan, South Korea
[3] Wonkwang Univ, Sch Med, Dept Lab Med, Iksan, South Korea
[4] Ewha Womans Univ, Ctr Cell Signalling Res, Seodaemoon Gu, Seoul, South Korea
[5] Ewha Womans Univ, Div Mol Life Sci, Seodaemoon Gu, Seoul, South Korea
[6] Korea Inst Sci & Technol, Natl Creat Res Initiat Ctr Calcium & Learning, Seoul 130650, South Korea
[7] NHLBI, Lab Cell Signaling, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1182/blood-2002-08-2548
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Peroxiredoxins (Prxs) are a family of antioxidant proteins that reduce peroxide levels by using reducing agents such as thioredoxin. These proteins were characterized to have a number of cellular functions, including cell proliferation and differentiation and protection of specific proteins from oxidative damage. However, the physiological roles of the peroxiredoxins have not been determined. To clarify the physiological relevance of this protein type, we generated a mouse model deficient in Prx II, which is abundantly expressed in all types of cells. The Prx II-/- mice were healthy in appearance and fertile. However, they had splenomegaly caused by the congestion of red pulp with hemosiderin accumulation. Heinz bodies were detected in their peripheral blood, and morphologically abnormal cells were elevated in the dense red blood cell (RBC) fractions, which contained markedly higher levels of reactive oxygen species (ROS). The Prx II-/- mice had significantly decreased hematocrit levels, but increased reticulocyte counts and erythropoletin levels, indicative of a compensatory action to maintain hematologic homeostasis in the mice. In addition, a labeling experiment with the thiol-modifying reagent biotinylated iodoacetamide (BIAM) in Prx II-/- mice revealed that a variety of RBC proteins were highly oxidized. Our results suggest that Prx II-/- mice have hemolytic anemia and that Prx II plays a major role in protecting RBCs from oxidative stress in mice. (C) 2003 by The American Society of Hematology.
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页码:5033 / 5038
页数:6
相关论文
共 31 条
[1]  
BARONCIANI L, 1994, BLOOD, V84, P2354
[2]   Identification of the disulfide-linked peptide in irreversibly sickled cell beta-actin [J].
Bencsath, FA ;
Shartava, A ;
Monteiro, CA ;
Goodman, SR .
BIOCHEMISTRY, 1996, 35 (14) :4403-4408
[3]  
BEUTLER E, 1990, BLOOD, V75, P271
[4]  
Beutler E, 1994, Rev Invest Clin, VSuppl, P162
[5]  
BEUTLER E, 1990, Hematologic Pathology, V4, P103
[6]   G6PD DEFICIENCY [J].
BEUTLER, E .
BLOOD, 1994, 84 (11) :3613-3636
[7]   Interaction of human thiol-specific antioxidant protein 1 with erythrocyte plasma membrane [J].
Cha, MK ;
Yun, CH ;
Kim, IH .
BIOCHEMISTRY, 2000, 39 (23) :6944-6950
[8]  
CHAE HZ, 1993, J BIOL CHEM, V268, P16815
[9]   Mice with a homozygous null mutation for the most abundant glutathione peroxidase, Gpx1, show increased susceptibility to the oxidative stress-inducing agents paraquat and hydrogen peroxide [J].
de Haan, JB ;
Bladier, C ;
Griffiths, P ;
Kelner, M ;
O'Shea, RD ;
Cheung, NS ;
Bronson, RT ;
Silvestro, MJ ;
Wild, S ;
Zheng, SS ;
Beart, PM ;
Hertzog, PJ ;
Kola, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22528-22536
[10]   Signal transduction - A bridge to control [J].
Demple, B .
SCIENCE, 1998, 279 (5357) :1655-1656