Bachem M G, Riess U, Gressner A M
Department of Clinical Chemistry, Philipps-University, Marburg, FRG.
Biochem Biophys Res Commun. 1989 Jul 31;162(2):708-14. doi: 10.1016/0006-291x(89)92368-1.
Human epidermal growth factor (EGF) and rat recombinant transforming growth factor alpha (TGFa) stimulated in a dose dependent manner the proliferation of rat liver fat storing cells (FSC) grown as primary culture in Dulbecco's modification of Eagles medium (DMEM) with 0.5% fetal calf serum (FCS). Cell proliferation was measured by DNA-content, [3H]thymidine- and bromodeoxyuridine-incorporation, respectively. Half maximal stimulation of [3H]thymidine incorporation was seen with 8ng/ml EGF and 7 ng/ml TGFa, respectively. In a radioreceptor assay using [125I]EGF as ligand TFGa binds with the same affinity as EGF to EGF-cell surface receptors on FSC. Eight ng/ml TGFa was required to produce half-maximal inhibition of [125I]EGF binding. If transforming growth factor beta (TGF beta) was added simultaneously with EGF or TGFa, FSC proliferation was inhibited strongly.
人表皮生长因子(EGF)和大鼠重组转化生长因子α(TGFα)以剂量依赖方式刺激在含有0.5%胎牛血清(FCS)的杜尔贝科改良伊格尔培养基(DMEM)中作为原代培养生长的大鼠肝脏贮脂细胞(FSC)的增殖。分别通过DNA含量、[3H]胸腺嘧啶核苷掺入和溴脱氧尿苷掺入来测量细胞增殖。[3H]胸腺嘧啶核苷掺入的半数最大刺激分别在8ng/ml EGF和7ng/ml TGFα时出现。在使用[125I]EGF作为配体的放射受体测定中,TFGα与EGF以相同亲和力结合到FSC上的EGF细胞表面受体。需要8ng/ml TGFα才能产生[125I]EGF结合的半数最大抑制。如果转化生长因子β(TGFβ)与EGF或TGFα同时添加,则FSC增殖受到强烈抑制。