Quinn G, Ochiya T, Terada M, Yoshida T
Genetics Division, National Cancer Centre Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Biochem Biophys Res Commun. 2000 Oct 5;276(3):1089-99. doi: 10.1006/bbrc.2000.3602.
The endothelial-specific receptor tyrosine kinase flt-1 (VEGFR-1) is expressed early on during endothelial lineage commitment both in vivo and in vitro. However, the exact function of flt-1 in vascular development still remains unclear. Here we report that a 2.2-kb fragment 5' of the mouse flt-1 gene becomes transcriptionally active during endothelial cell differentiation in developing embryoid bodies derived from mouse ES cells. Reporter gene expression correlated well with PECAM-1 expression and mirrored the expression pattern of the endogenous flt-1 gene. The temporal and spatial activity of the 2.2-kb flt-1 promoter provides a means to (1) identify a living population of early committed endothelial/bipotential progenitors and (2) ectopically express biologically active genes during lineage commitment.
内皮特异性受体酪氨酸激酶flt-1(血管内皮生长因子受体-1,VEGFR-1)在体内和体外内皮细胞系定向分化的早期均有表达。然而,flt-1在血管发育中的具体功能仍不清楚。在此我们报告,小鼠flt-1基因5'端一个2.2 kb的片段,在源自小鼠胚胎干细胞的发育中的拟胚体内皮细胞分化过程中变得具有转录活性。报告基因表达与血小板内皮细胞黏附分子-1(PECAM-1)的表达密切相关,并反映了内源性flt-1基因的表达模式。2.2 kb flt-1启动子的时空活性提供了一种方法,可用于(1)鉴定早期定向分化的内皮/双能祖细胞的存活群体,以及(2)在细胞系定向分化过程中异位表达生物活性基因。