Onagbesan O M, Peddie M J
Department of Physiology and Pharmacology, University of Southampton, Bassett Crescent East, UK.
Histochem J. 1998 Sep;30(9):647-56. doi: 10.1023/a:1003544926637.
Epidermal growth factor (EGF) and transforming growth factor alpha (TGF-alpha) are structurally related growth factors that exert their biological actions by binding to the same cell-surface receptor, EGF receptor. However, in chicken cells, human EGF binds with approximately 100-fold lower affinity than human TGF-alpha. In a previous study, we localized EGF/TGF-alpha receptor immunohistochemically in the granulosa and theca of the developing follicles of laying hens. We have also shown that TGF-alpha binds to cell-surface receptors of the granulosa cells. The present study characterizes the nature of the EGF/TGF-alpha receptor. Immunoprecipitation of receptor proteins from cultured granulosa cells with an anti-EGF receptor antibody (12E) shows the expression of a 170-kDa receptor protein. The expression of the receptor protein decreases with follicular enlargement between the F3 and F1. Incubation of the cells with [125I]TGF-alpha followed by cross-linking with bis(sulphosuccinimidyl)suberate showed that TGF-alpha binds a similar (170 kDa) receptor protein immunoprecipitated with the 12E anti-EGF receptor antibody. The binding of TGF-alpha to granulosa cells caused receptor protein oligomerization, yielding the monomeric (170 kDa) and dimeric (340 kDa) protein forms. Oligomerization seemed to favour the formation of the dimeric rather than the monomeric form. Culturing granulosa cells with luteinizing hormone or follicle-stimulating hormone increased the expression of both monomer and dimer forms of the receptor proteins compared with the control. Western blotting analysis with anti-phosphotyrosine antibody revealed that the lysates of TGF-alpha-stimulated cells express phosphotyrosine-containing receptor proteins of 170 kDa and 340 kDa. The results show that chicken granulosa cells express the 170-kDa EGF/TGF-alpha receptor protein, which dimerizes on binding to TGF-alpha, suggesting that the receptor protein may be involved in the signal transduction of TGF-alpha actions in the chicken granulosa cells.
表皮生长因子(EGF)和转化生长因子α(TGF-α)是结构相关的生长因子,它们通过与同一细胞表面受体即EGF受体结合来发挥生物学作用。然而,在鸡细胞中,人EGF的结合亲和力比人TGF-α低约100倍。在先前的一项研究中,我们通过免疫组织化学方法将EGF/TGF-α受体定位在产蛋母鸡发育卵泡的颗粒细胞和卵泡膜细胞中。我们还表明TGF-α与颗粒细胞的细胞表面受体结合。本研究对EGF/TGF-α受体的性质进行了表征。用抗EGF受体抗体(12E)从培养的颗粒细胞中免疫沉淀受体蛋白,结果显示有170 kDa受体蛋白的表达。在F3和F1之间,随着卵泡增大,受体蛋白的表达降低。用[125I]TGF-α孵育细胞,随后用双(磺基琥珀酰亚胺基)辛二酸酯进行交联,结果显示TGF-α与用12E抗EGF受体抗体免疫沉淀的类似(170 kDa)受体蛋白结合。TGF-α与颗粒细胞的结合导致受体蛋白寡聚化,产生单体(170 kDa)和二聚体(340 kDa)蛋白形式。寡聚化似乎有利于二聚体而非单体形式的形成。与对照组相比,用促黄体生成素或促卵泡激素培养颗粒细胞可增加受体蛋白单体和二聚体形式的表达。用抗磷酸酪氨酸抗体进行的蛋白质印迹分析表明,TGF-α刺激细胞的裂解物表达含磷酸酪氨酸的170 kDa和340 kDa受体蛋白。结果表明,鸡颗粒细胞表达170 kDa的EGF/TGF-α受体蛋白,该蛋白在与TGF-α结合时会二聚化,这表明该受体蛋白可能参与了TGF-α在鸡颗粒细胞中作用的信号转导。