Henkel G W, McKercher S R, Yamamoto H, Anderson K L, Oshima R G, Maki R A
Burnham Institute, La Jolla Cancer Research Foundation, CA 92037, USA.
Blood. 1996 Oct 15;88(8):2917-26.
Transcription factors play an important role choreographing lineage commitment and expansion of blood cells. Nuclear factors that are expressed primarily or exclusively in hematopoietic cells are likely candidates for regulating blood cell development. The transcription factor PU.1 is found only in hematopoietic cells, whereas ets-2, a related family member, is ubiquitously expressed. To compare the role of these two transcription factors in macrophage development, embryonic stem (ES) cells with a homozygous disruption of either the PU.1 or the ets-2 gene were generated. The ability of both knockout ES cells to differentiate to macrophages was tested. Normal development of macrophages, as determined by histochemical and immunohistochemical analysis, from PU.1 knockout ES cells was significantly blocked. Furthermore, the expression of known markers associated with macrophages, such as c-fms, CD11b, CD18 and granulocyte-macrophage colony-stimulating factor receptor, were not detected by reverse transcriptase-polymerase chain reaction. In contrast to the PU.1 knockout ES cells, macrophages, development from the ets-2 knockout ES cells was normal. Although both PU.1 and ets-2 are found in macrophages, these data show a distinct role for the lineage-restricted PU.1 transcription factor in macrophage development.
转录因子在编排血细胞谱系定向分化和增殖过程中发挥着重要作用。主要或仅在造血细胞中表达的核因子可能是调节血细胞发育的候选因子。转录因子PU.1仅在造血细胞中发现,而相关家族成员ets-2则广泛表达。为了比较这两种转录因子在巨噬细胞发育中的作用,构建了分别纯合缺失PU.1或ets-2基因的胚胎干细胞(ES细胞)。检测了两种基因敲除ES细胞分化为巨噬细胞的能力。通过组织化学和免疫组织化学分析确定,PU.1基因敲除ES细胞中巨噬细胞的正常发育受到显著阻碍。此外,逆转录聚合酶链反应未检测到与巨噬细胞相关的已知标志物如c-fms、CD11b、CD18和粒细胞-巨噬细胞集落刺激因子受体的表达。与PU.1基因敲除ES细胞相反,ets-2基因敲除ES细胞中巨噬细胞发育正常。尽管PU.1和ets-2都存在于巨噬细胞中,但这些数据表明谱系限制的PU.1转录因子在巨噬细胞发育中具有独特作用。