生物活性多肽受体的遗传学:人EGF受体基因的表达和受体结合的EGF在人-小鼠杂交细胞中的内化和加工。

M A Behzadian, Y Shimizu, I Kondo, N Shimizu
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引用次数: 13

摘要

我们先前假设表皮生长因子(EGF)受体的结构基因位于人类7号染色体上(1,2)。在本研究中,我们在一个独特的细胞杂交系C2B5中进一步分析了EGF受体和某些后受体功能,C2B5除了几乎完整的小鼠亲本基因组外,只保留了一条X;7易位的人类染色体。[125I]EGF与C2B5杂交细胞结合的动力学和Scatchard分析表明,它们携带单类EGF受体,解离常数为4 × 10(-10) m。杂交细胞中表达的受体在免疫学上被证明是人性的。现在嵌入小鼠质膜的人EGF受体受到EGF配体介导的“下调”。细胞结合的EGF分析表明,内化和加工发生在人-小鼠细胞杂交中。EGF的降解似乎是通过溶酶体途径,因为它基本上被溶酶体药物延迟或抑制。
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Genetics of receptors for bioactive polypeptides: expression of the human EGF receptor gene and internalization and processing of the receptor-bound EGF in human-mouse cell hybrids.

We previously postulated that the structural gene for epidermal growth factor (EGF) receptor is located on human chromosome 7 (1,2). In this study, EGF receptor and certain postreceptor functions were further analyzed in a unique cell hybrid line, C2B5, that retains only one human chromosome of an X;7 translocation besides a nearly complete mouse parental genome. Kinetics and Scatchard analysis of [125I]EGF binding to the C2B5 hybrid cells indicated that they carry a single class of EGF receptors with a dissociation constant of 4 x 10(-10) M. The receptors expressed in the hybrids are proven to be immunologically of human nature. The human EGF receptors now embedded in essentially mouse plasma membrane are subject to "down regulation" mediated by the ligand EGF. Analysis of the cell-bound EGF indicated that internalization and processing take place in the human-mouse cell hybrids. The degradation of EGF appears to be through a lysosomal pathway since it was substantially delayed or inhibited by lysosomotropic agents.

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