B- and T-cell-specific inactivation of thioredoxin reductase 2 does not impair lymphocyte development and maintenance

被引:16
作者
Geisberger, Roland
Kiermayer, Claudia
Hoemig, Cornelia
Conrad, Marcus
Schmidt, Joerg
Zimber-Strobl, Ursula
Brielmeier, Markus
机构
[1] GSF, Res Ctr Environm & Hlth, Dept Comparat Med, D-85764 Neuherberg, Germany
[2] GSF, Res Ctr Environm & Hlth, Inst Clin Mol Bil & Tumor Genet, D-85764 Neuherberg, Germany
关键词
CD4-Cre; CD19-Cre; conditional knockout; lymphocyte; selenoprotein;
D O I
10.1515/BC.2007.131
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Thioredoxin reductases (Txnrds) are a group of seleno-enzymes participating in cellular redox regulation. Three Txnrd isoforms are known, each of which exhibits distinct cellular localisation and tissue-specific expression pattern. Txnrd1 is found in the cytoplasm, expression of Txnrd2 is restricted to mitochondria and Txnrd3 shows testis-specific expression. Recently, it was shown that Txnrd2 strongly affects the development of blood cells, since mouse embryos deficient for Txnrd2 are severely anaemic, show increased apoptosis in foetal liver and possess haematopoietic liver stem cells of reduced capacity to proliferate in vitro. However, because Txnrd2-deficient mice die at embryonic day 13.5, it was not known how this enzyme affects blood cell function in the adult animal. In the present study we show that conditional Txnrd2 knockouts generated using CD4(-) and CD19Cre transgenic mice lack Txnrd2 expression in CD4(-)- and CID19-positive T- and B-lymphocytes, respectively. However, the development and differentiation of both cell types in thymus and bone marrow was not significantly impaired. In addition, B-cell proliferation and activation in response to CD40 and IL-4 was unaltered in Txnrd2-deficient B-cells.
引用
收藏
页码:1083 / 1090
页数:8
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