Yarden Y, Schreiber A B, Schlessinger J
J Cell Biol. 1982 Mar;92(3):687-93. doi: 10.1083/jcb.92.3.687.
Cyanogen bromide-cleaved epidermal growth factor (CNBr-EGF) binds to EGF receptors with reduced affinity compared to the native hormone but fails to induce DNA synthesis. However, at similar receptor occupancy, CNBr-EGF is as potent as EGF in activating early cell responses to the hormone. The phosphorylation of membrane proteins, the stimulation of Na+-K+-ATPase as reflected by the ouabain-sensitive uptake of 86Rb of fibroblasts, changes in the organization of microfilaments and in cell-morphology, and the activation of the enzyme ornithine-decarboxylase are all induced by CNBr-EGF as well as EGF Our results are consistent with the notion that EGF-induced phosphorylation could act as a "second messenger" for the action of various EGF-induced responses such as activation of Na+-K+-ATPase, changes in the cytoskeleton and cell morphology, and the activation of the enzyme ornithine decarboxylase. However, the stimulation of phosphorylation of membrane proteins and other early responses are either not required or necessary but insufficient for the induction of DNA synthesis. Suboptimal concentrations of EGF together with CNBr-EGF stimulate DNA synthesis in human fibroblasts. Other growth factors such as insulin, fibroblast growth factor, and prostaglandin F2 alpha, which potentiate the mitogenic response of EGF, do not effect the response to CNBr-EGF. This suggests that the restoration of the mitogenic properties of CNBr-EGF by suboptimal doses of EGF occurs at the level of EGF receptors or during their processing.
溴化氰裂解的表皮生长因子(CNBr-EGF)与天然激素相比,以降低的亲和力结合表皮生长因子受体,但不能诱导DNA合成。然而,在相似的受体占有率下,CNBr-EGF在激活细胞对该激素的早期反应方面与EGF一样有效。膜蛋白的磷酸化、成纤维细胞对哇巴因敏感的86Rb摄取所反映的Na+-K+-ATP酶的刺激、微丝组织和细胞形态的变化以及鸟氨酸脱羧酶的激活均由CNBr-EGF和EGF诱导。我们的结果与以下观点一致,即EGF诱导的磷酸化可作为各种EGF诱导反应(如Na+-K+-ATP酶的激活、细胞骨架和细胞形态的变化以及鸟氨酸脱羧酶的激活)作用的“第二信使”。然而,膜蛋白磷酸化的刺激和其他早期反应对于DNA合成的诱导要么不是必需的,要么是必需的但不足以诱导DNA合成。次优浓度的EGF与CNBr-EGF一起可刺激人成纤维细胞中的DNA合成。其他生长因子,如胰岛素、成纤维细胞生长因子和前列腺素F2α,可增强EGF的促有丝分裂反应,但不影响对CNBr-EGF的反应。这表明,次优剂量的EGF恢复CNBr-EGF的促有丝分裂特性发生在EGF受体水平或其加工过程中。