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FRTL-5大鼠甲状腺滤泡细胞系中胰岛素样生长因子-I受体的特性与调控

Characterization and regulations of the receptor for insulin-like growth factor-I in the FRTL-5 rat thyroid follicular cell line.

作者信息

Tramontano D, Moses A C, Picone R, Ingbar S H

出版信息

Endocrinology. 1987 Feb;120(2):785-90. doi: 10.1210/endo-120-2-785.

Abstract

In previous studies we have shown that insulin-like growth factor I (IGF-I) has a mitogenic effect in a line of rat thyroid follicular cells, the FRTL-5. In view of this effect, we undertook studies to identify and characterize some physicochemical and binding properties of the receptor for IGF-I in these cells and to determine what role it plays in the mitogenic activity of insulin and insulin-like growth factors in the FRTL-5 cell. Binding of 125I-labeled IGF-I (biosynthetic Thr59-IGF-I) to FRTL-5 was a function of time, temperature, and pH and was completely inhibited by high concentrations of unlabeled IGF-I. Scatchard plots of four saturation studies revealed a single apparent binding site with an average Ka of 4.2 +/- 0.6 X 10(9) M-1 (mean +/- SD) and an average maximum binding capacity of 20 +/- 2 pm/100 micrograms cellular protein. Rat IGF-II (rIGF-II) and insulin were far less potent that IGF-I in inhibiting the binding of [125I] IGF-I, and bovine TSH was without effect. 125I-Labeled IGF-II also bound to FRTL-5 cells. Binding was completely inhibited by unlabeled rIGF-II and, with lesser potency, by IGF-I. Even at high concentrations, insulin failed to inhibit the binding of [125I]IGF-II. Disuccinimidyl suberate cross-linked [125I]IGF-I to a moiety in FRTL-5 that had an apparent mol wt of approximately 135,000, as judged from sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions. Cross-linking of [125I]IGF-I was inhibited in a dose-dependent manner by unlabeled IGF-I and, with far lower potency, by rIGF-II and insulin. All three peptides stimulated the incorporation of [3H]thymidine into the DNA of FRTL-5 cells, IGF-I being the most potent, followed in decreasing order of potency of rIGF-II and insulin. The mitogenic activities of these polypeptides correlated well with their abilities to inhibit the binding of [125I]IGF-I. These data indicate that the FRTL-5 cell possesses a receptor for IGF-I that resembles in its binding and physicochemical properties the receptor for IGF-I in other tissues (type I IGF receptor) and that mediates the mitogenic response to IGF-I and insulin in these cells. FRTL-5 cells also contain a receptor for IGF-II (type II IGF receptor), but its role vis-à-vis that of the type I IGF receptor in relation to the mitogenic effect of IGF-II in these cells is uncertain.

摘要

在先前的研究中,我们已经表明胰岛素样生长因子I(IGF-I)对大鼠甲状腺滤泡细胞系FRTL-5具有促有丝分裂作用。鉴于这种作用,我们进行了研究,以鉴定和表征这些细胞中IGF-I受体的一些物理化学和结合特性,并确定其在FRTL-5细胞中胰岛素和胰岛素样生长因子的促有丝分裂活性中所起的作用。125I标记的IGF-I(生物合成的Thr59-IGF-I)与FRTL-5的结合是时间、温度和pH的函数,并被高浓度的未标记IGF-I完全抑制。四项饱和研究的Scatchard图显示有一个单一的表观结合位点,平均解离常数Ka为4.2±0.6×10⁹ M⁻¹(平均值±标准差),平均最大结合容量为20±2 pm/100微克细胞蛋白。大鼠IGF-II(rIGF-II)和胰岛素在抑制[125I]IGF-I结合方面的效力远低于IGF-I,而牛促甲状腺激素则无作用。125I标记的IGF-II也与FRTL-5细胞结合。未标记的rIGF-II可完全抑制结合,IGF-I的抑制效力较小。即使在高浓度下,胰岛素也不能抑制[125I]IGF-II的结合。在还原条件下进行的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示,辛二酸二琥珀酰亚胺酯将[125I]IGF-I交联到FRTL-5中一个表观分子量约为135,000的部分。未标记的IGF-I以剂量依赖性方式抑制[125I]IGF-I的交联,rIGF-II和胰岛素的抑制效力则低得多。所有这三种肽都刺激[3H]胸腺嘧啶掺入FRTL-5细胞的DNA中,IGF-I的效力最强,其次是rIGF-II和胰岛素,效力依次降低。这些多肽的促有丝分裂活性与其抑制[125I]IGF-I结合的能力密切相关。这些数据表明,FRTL-5细胞拥有一种IGF-I受体,其结合和物理化学特性类似于其他组织中的IGF-I受体(I型IGF受体),并介导这些细胞对IGF-I和胰岛素的促有丝分裂反应。FRTL-5细胞还含有一种IGF-II受体(II型IGF受体),但其在这些细胞中相对于I型IGF受体在IGF-II促有丝分裂作用方面的作用尚不确定。

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