Adamson E D, Rees A R
Mol Cell Biochem. 1981 Feb 11;34(3):129-52. doi: 10.1007/BF02359619.
EGF-Rs are cell membrane glycoproteins of wide distribution. They have not yet been fully characterized or purified but are probably molecules of 170-190,000 mol. wt. in most cells. The growth factor EGF binds and will saturate cell surface receptors with a KA of about 5 X 10(9) M-1 although a receptor class with an affinity in excess of 10(10) M-1 has been detected in some cells. The number of receptors on a cell does not determine the level of its response. Some cell types have receptors which bind EGF, but with no mitogenic response. The ways in which receptor affinity and/or number is modulated are described. This and other evidence is reviewed in a search for a suitable model of a mechanism of action on the cell, which best fits the current data. There is ample evidence that EGF binds to the receptor; that ligand-receptor complexes cluster or aggregate; and then are internalized and degraded, but evidence for a direct connection between internalization and the subsequent mitogenic response is lacking. Good correlations between internalization and mitogenic responses have been observed and developed into a theory of endocytic activation, but there is a body of evidence which cannot be accommodated by this theory. Instead, an alternative model is suggested.
表皮生长因子受体(EGF-Rs)是广泛分布的细胞膜糖蛋白。它们尚未得到充分的表征或纯化,但在大多数细胞中可能是分子量为170,000 - 190,000道尔顿的分子。生长因子表皮生长因子(EGF)能结合并使细胞表面受体饱和,其解离常数(KA)约为5×10⁹ M⁻¹,不过在某些细胞中已检测到一类亲和力超过10¹⁰ M⁻¹的受体。细胞上受体的数量并不能决定其反应水平。一些细胞类型具有能结合EGF的受体,但却没有促有丝分裂反应。文中描述了受体亲和力和/或数量被调节的方式。为了寻找一种最符合当前数据的、合适的细胞作用机制模型,对这一证据及其他证据进行了综述。有充分的证据表明EGF与受体结合;配体 - 受体复合物会聚集;然后被内化并降解,但缺乏内化与随后的促有丝分裂反应之间直接联系的证据。已观察到内化与促有丝分裂反应之间存在良好的相关性,并发展成一种内吞激活理论,但有一些证据无法用该理论来解释。相反,本文提出了一种替代模型。