Takehara K, LeRoy E C, Grotendorst G R
Cell. 1987 May 8;49(3):415-22. doi: 10.1016/0092-8674(87)90294-7.
Transforming growth factor-beta (TGF-beta) inhibits the growth of endothelial cells derived from various sources, including human umbilical vein, bovine aorta, and rat heart. Long-term exposure of rat heart endothelial cells to TGF-beta also induces dramatic changes in morphology that are characteristic of senescent cells. These changes are accompanied by a decrease in the number of high-affinity receptors for epidermal growth factor (EGF), with almost no change in total receptor number. Additionally, the EGF-induced expression of specific competence genes (c-myc, JE, KC) is decreased, whereas the induction of c-fos gene expression by EGF is unaltered by TGF-beta treatment. These data suggest that growth inhibitors such as TGF-beta may act by altering the cell's response to growth-stimulatory factors.
转化生长因子-β(TGF-β)可抑制源自多种来源的内皮细胞生长,包括人脐静脉、牛主动脉和大鼠心脏。大鼠心脏内皮细胞长期暴露于TGF-β也会诱导出衰老细胞特有的形态学显著变化。这些变化伴随着表皮生长因子(EGF)高亲和力受体数量的减少,而总受体数量几乎没有变化。此外,EGF诱导的特定能力基因(c-myc、JE、KC)的表达降低,而EGF诱导的c-fos基因表达不受TGF-β处理的影响。这些数据表明,诸如TGF-β之类的生长抑制剂可能通过改变细胞对生长刺激因子的反应来发挥作用。