Sugino H, Nakamura T, Hasegawa Y, Miyamoto K, Igarashi M, Eto Y, Shibai H, Titani K
Frontier Research Program, Institute of Physical and Chemical Research, Saitama, Japan.
J Biol Chem. 1988 Oct 25;263(30):15249-52.
A cellular receptor for erythroid differentiation factor (EDF) was demonstrated by incubation of 125I-labeled EDF with rat follicular granulosa cell cultures. The specific binding of labeled EDF to the cells showed saturation; Scatchard analysis of binding data indicated a single class of receptors having Kd = 3.4 x 10(-10) M. A large excess of unlabeled EDF reduced labeled EDF binding almost completely, whereas similar doses of inhibin and transforming growth factor type beta, which are quite similar to EDF in protein structure and subunit organization, had no effect; EDF did not share receptors with those factors. EDF receptor (activin A receptor) expression was enhanced in granulosa cells cultured in the presence of follicle-stimulating hormone; follicle-stimulating hormone raised the number of EDF binding sites/cell from 13,000 to 96,000 without altering the binding affinity.
通过将125I标记的红细胞分化因子(EDF)与大鼠卵泡颗粒细胞培养物孵育,证明了一种EDF细胞受体。标记的EDF与细胞的特异性结合呈现饱和状态;结合数据的Scatchard分析表明存在一类单一的受体,其解离常数(Kd)= 3.4×10^(-10) M。大量未标记的EDF几乎完全降低了标记的EDF结合,而类似剂量的抑制素和β型转化生长因子,它们在蛋白质结构和亚基组成上与EDF非常相似,却没有作用;EDF与这些因子不共享受体。在促卵泡激素存在下培养的颗粒细胞中,EDF受体(激活素A受体)的表达增强;促卵泡激素使每个细胞的EDF结合位点数量从13,000增加到96,000,而不改变结合亲和力。