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人胎盘和蜕膜中不同的胰岛素样生长因子结合种类。

Different insulin-like growth factor binding species in human placenta and decidua.

作者信息

Pekonen F, Suikkari A M, Mäkinen T, Rutanen E M

机构信息

Minerva Institute for Medical Research, Kauniainen, Finland.

出版信息

J Clin Endocrinol Metab. 1988 Dec;67(6):1250-7. doi: 10.1210/jcem-67-6-1250.

Abstract

Previous studies demonstrated that human decidua secretes a 34K insulin-like growth factor binding protein (34K IGF-BP) earlier designated placental protein 12, whereas placenta contains IGF receptors and IGF mRNA. We studied binding of [125I]IGF-I to paired placental and decidual tissues using competitive binding, gel filtration, RIA, and cross-linking techniques, and compared the binding characteristics of these two tissues which are located in close proximity in vivo. The effect of decidual cytosols on [125I]IGF-I binding to placental membranes also was studied. Consistent with previous data the dominating binding species in placental membranes were IGF receptors. In contrast, the binding of [125I]IGF-I to decidual membranes was mainly due to binding species with mol wts of 34K and 39K. The 34K IGF-BP was more readily detected in decidual cytosols than in decidual membranes and little was detected in placental cytosols. Purified 34K IGF-BP as well as decidual cytosols inhibited [125I]IGF-I binding to placental receptors. The inhibitory effect of decidual cytosol on IGF receptor binding was linearly correlated to the decidual content of 34K IGF-BP. The results suggest that the decidual 34K IGF-BP might act as a local modulator of the IGF action at the interface between the decidua and the placenta.

摘要

以往的研究表明,人蜕膜分泌一种34K胰岛素样生长因子结合蛋白(34K IGF-BP),该蛋白先前被命名为胎盘蛋白12,而胎盘含有IGF受体和IGF mRNA。我们采用竞争性结合、凝胶过滤、放射免疫分析和交联技术研究了[125I]IGF-I与配对的胎盘和蜕膜组织的结合,并比较了这两种在体内紧密相邻的组织的结合特性。还研究了蜕膜胞质溶胶对[125I]IGF-I与胎盘膜结合的影响。与先前的数据一致,胎盘膜中主要的结合物质是IGF受体。相比之下,[125I]IGF-I与蜕膜的结合主要是由于分子量为34K和39K的结合物质。34K IGF-BP在蜕膜胞质溶胶中比在蜕膜中更容易检测到,而在胎盘胞质溶胶中几乎检测不到。纯化的34K IGF-BP以及蜕膜胞质溶胶均抑制[125I]IGF-I与胎盘受体的结合。蜕膜胞质溶胶对IGF受体结合的抑制作用与34K IGF-BP的蜕膜含量呈线性相关。结果表明,蜕膜34K IGF-BP可能作为蜕膜与胎盘界面处IGF作用的局部调节剂。

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