Coppola D, Ferber A, Miura M, Sell C, D'Ambrosio C, Rubin R, Baserga R
Jefferson Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Mol Cell Biol. 1994 Jul;14(7):4588-95. doi: 10.1128/mcb.14.7.4588-4595.1994.
When wild-type mouse embryo cells are stably transfected with a plasmid constitutively overexpressing the epidermal growth factor (EGF) receptor (EGFR), the resulting cells can grow in serum-free medium supplemented solely with EGF. Supplementation with EGF also induces in these cells the transformed phenotype (growth in soft agar). However, when the same EGFR expression plasmid is introduced and overexpressed in cells derived from littermate embryos in which the insulin-like growth factor I (IGF-I) receptor genes have been disrupted by homologous recombination, the resulting cells are unable to grow or to be transformed by the addition of EGF. Reintroduction into these cells (null for the IGF-I receptor) of a wild-type (but not of a mutant) IGF-I receptor restores EGF-mediated growth and transformation. Our results indicate that at least in mouse embryo fibroblasts, the EGFR requires the presence of a functional IGF-I receptor for its mitogenic and transforming activities.
当野生型小鼠胚胎细胞用组成型过表达表皮生长因子(EGF)受体(EGFR)的质粒进行稳定转染时,所得细胞能够在仅补充有EGF的无血清培养基中生长。补充EGF还会在这些细胞中诱导转化表型(在软琼脂中生长)。然而,当相同的EGFR表达质粒被导入并在来自同窝胚胎的细胞中过表达,其中胰岛素样生长因子I(IGF-I)受体基因已通过同源重组被破坏时,所得细胞无法通过添加EGF生长或被转化。将野生型(而非突变型)IGF-I受体重新导入这些细胞(IGF-I受体缺失)可恢复EGF介导的生长和转化。我们的结果表明,至少在小鼠胚胎成纤维细胞中,EGFR的促有丝分裂和转化活性需要功能性IGF-I受体的存在。