Barrantes Ivan del Barco, Montero-Pedrazuela Ana, Guadaño-Ferraz Ana, Obregon Maria-Jesus, Martinez de Mena Raquel, Gailus-Durner Valérie, Fuchs Helmut, Franz Tobias J, Kalaydjiev Svetoslav, Klempt Martina, Hölter Sabine, Rathkolb Birgit, Reinhard Claudia, Morreale de Escobar Gabriella, Bernal Juan, Busch Dirk H, Wurst Wolfgang, Wolf Eckhard, Schulz Holger, Shtrom Svetlana, Greiner Erich, Hrabé de Angelis Martin, Westphal Heiner, Niehrs Christof
Division of Molecular Embryology, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.
Mol Cell Biol. 2006 Mar;26(6):2317-26. doi: 10.1128/MCB.26.6.2317-2326.2006.
dickkopf (dkk) genes encode a small family of secreted Wnt antagonists, except for dkk3, which is divergent and whose function is poorly understood. Here, we describe the generation and characterization of dkk3 mutant mice. dkk3-deficient mice are viable and fertile. Phenotypic analysis shows no major alterations in organ morphology, physiology, and most clinical chemistry parameters. Since Dkk3 was proposed to function as thyroid hormone binding protein, we have analyzed deiodinase activities, as well as thyroid hormone levels. Mutant mice are euthyroid, and the data do not support a relationship of dkk3 with thyroid hormone metabolism. Altered phenotypes in dkk3 mutant mice were observed in the frequency of NK cells, immunoglobulin M, hemoglobin, and hematocrit levels, as well as lung ventilation. Furthermore, dkk3-deficient mice display hyperactivity.
迪克kopf(Dkk)基因编码一个分泌型Wnt拮抗剂的小家族,但Dkk3除外,它具有差异性且其功能了解甚少。在此,我们描述了Dkk3突变小鼠的产生和特征。Dkk3基因缺陷型小鼠可存活且可育。表型分析显示,其器官形态、生理学和大多数临床化学参数无重大改变。由于有人提出Dkk3可作为甲状腺激素结合蛋白发挥作用,我们分析了脱碘酶活性以及甲状腺激素水平。突变小鼠甲状腺功能正常,数据不支持Dkk3与甲状腺激素代谢之间存在关联。在Dkk3突变小鼠中,观察到自然杀伤细胞频率、免疫球蛋白M、血红蛋白和血细胞比容水平以及肺通气方面的表型改变。此外,Dkk3基因缺陷型小鼠表现出多动。