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p45NFE2基因缺陷小鼠红细胞中氧化应激反应减弱。

Reduced oxidative-stress response in red blood cells from p45NFE2-deficient mice.

作者信息

Chan J Y, Kwong M, Lo M, Emerson R, Kuypers F A

机构信息

Department of Laboratory Medicine, University of California, San Francisco 94143-0793, USA.

出版信息

Blood. 2001 Apr 1;97(7):2151-8. doi: 10.1182/blood.v97.7.2151.

DOI:10.1182/blood.v97.7.2151
PMID:11264184
Abstract

p45NF-E2 is a member of the cap 'n' collar (CNC)-basic leucine zipper family of transcriptional activators that is expressed at high levels in various types of blood cells. Mice deficient in p45NF-E2 that were generated by gene targeting have high mortality from bleeding resulting from severe thrombocytopenia. Surviving p45nf-e2(-/-) adults have mild anemia characterized by hypochromic red blood cells (RBCs), reticulocytosis, and splenomegaly. Erythroid abnormalities in p45nf-e2(-/-) animals were previously attributed to stress erythropoiesis caused by chronic bleeding and, possibly, ineffective erythropoiesis. Previous studies suggested that CNC factors might play essential roles in regulating expression of genes that protect cells against oxidative stress. In this study, we found that p45NF-E2-deficient RBCs have increased levels of reactive oxygen species and an increased susceptibility to oxidative-stress-induced damage. Deformability of p45NF-E2-deficient RBCs was markedly reduced with oxidative stress, and mutant cells had a reduced life span. One possible reason for increased sensitivity to oxidative stress is that catalase levels were reduced in mutant RBCs. These findings suggest a role for p45NF-E2 in the oxidative-stress response in RBCs and indicate that p45NF-E2 deficiency contributes to the anemia in p45nf-e2(-/-) mice. (Blood. 2001;97:2151-2158)

摘要

p45NF-E2是转录激活因子帽状结构域亮氨酸拉链(CNC)家族的成员,在多种血细胞中高表达。通过基因打靶产生的p45NF-E2缺陷小鼠因严重血小板减少导致出血而死亡率很高。存活的p45nf-e2(-/-)成年小鼠有轻度贫血,其特征为低色素性红细胞、网织红细胞增多和脾肿大。p45nf-e2(-/-)动物的红细胞异常以前被归因于慢性出血引起的应激性红细胞生成,也可能是无效红细胞生成。以前的研究表明,CNC因子可能在调节保护细胞免受氧化应激的基因表达中起重要作用。在本研究中,我们发现p45NF-E2缺陷的红细胞活性氧水平升高,对氧化应激诱导的损伤更敏感。氧化应激时,p45NF-E2缺陷红细胞的变形性明显降低,突变细胞的寿命缩短。对氧化应激敏感性增加的一个可能原因是突变红细胞中过氧化氢酶水平降低。这些发现提示p45NF-E2在红细胞氧化应激反应中起作用,并表明p45NF-E2缺陷导致p45nf-e2(-/-)小鼠贫血。(《血液》。2001年;97:2151 - 2158)

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