Lieu Yen K, Kumar Atul, Pajerowski Anthony G, Rogers Thomas J, Reddy E Premkumar
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14853-8. doi: 10.1073/pnas.0405338101. Epub 2004 Oct 4.
Previous reports have suggested that the protooncogene c-myb participates in T cell development in the thymus and mature T cell proliferation. We have generated two T cell-specific c-myb knockout mouse models, myb/LckCre and myb/CD4Cre. We have demonstrated that c-myb is required for the development of thymocytes at the DN3 stage, for survival and proliferation of double-positive thymocytes, for differentiation of single-positive CD4 and CD8 T cells, and for the proliferative responses of mature T cells. In addition, our data show that c-myb is directly involved in the formation of double-positive CD4+CD8+CD25+, CD4+CD25+, and CD8+CD25+ T cells, developmental processes that may imply a role for c-myb in autoimmune dysfunction.
先前的报道表明,原癌基因c-myb参与胸腺中T细胞的发育以及成熟T细胞的增殖。我们构建了两种T细胞特异性c-myb基因敲除小鼠模型,即myb/LckCre和myb/CD4Cre。我们已经证明,c-myb对于双阴性3期胸腺细胞的发育、双阳性胸腺细胞的存活和增殖、单阳性CD4和CD8 T细胞的分化以及成熟T细胞的增殖反应是必需的。此外,我们的数据表明,c-myb直接参与双阳性CD4+CD8+CD25+、CD4+CD25+和CD8+CD25+ T细胞的形成,这些发育过程可能暗示c-myb在自身免疫功能障碍中发挥作用。