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一种独特的胎盘催乳素受体:对胎儿生长的影响。

A unique placental lactogen receptor: implications for fetal growth.

作者信息

Freemark M, Comer M, Korner G, Handwerger S

出版信息

Endocrinology. 1987 May;120(5):1865-72. doi: 10.1210/endo-120-5-1865.

Abstract

To determine whether there are structural differences between the binding sites for placental lactogen (PL) and GH, we have compared the molecular weights of complexes formed by the covalent cross-linking of [125I]ovine (o) PL and [125I]oGH to hepatic membranes from fetal and pregnant sheep in mid- and late gestation and from postnatal nonpregnant sheep at 3 days to 7 months of age. Specific [125I]oPL binding sites in fetal liver were detected as early as midgestation, and cross-linking of [125I]oPL to fetal hepatic membranes yielded a major radiographic band with a mol wt of 60 +/- 5 K (mean +/- SD). Unlabeled oPL at low concentrations (0.9-9 nM) specifically competed with [125I]oPL for binding to the 60 K complex. In contrast, oGH and oPRL competed for binding to the 60 K complex only at much higher concentrations (greater than or equal to 90 nM). In addition, no specific cross-linking of [125I]oGH or [125I]oPRL to fetal hepatic membranes was observed. These findings suggest the presence of a distinct and unique PL binding site in ovine fetal liver. Since the mol wt of oPL is 22 K, the estimated mol wt of the oPL receptor protein is 38 +/- 5 K. During the first week after birth, there was a striking increase in the number of [125I]oGH binding sites. Cross-linking of [125I]oGH to postnatal liver yielded radiographic bands with apparent mol wts of 75 K and 140 K. The relative potencies of oPL, oGH, and oPRL in competing for binding to the 75 K and 140 K complexes were similar to the relative potencies of these hormones in competing for [125I]oGH binding sites in postnatal liver, suggesting that the 75 K and 140 K bands represent subunits of the oGH receptor bound covalently to [125I]oGH. Cross-linking of [125I]oPL to pregnant and postnatal nonpregnant liver yielded three radiographic bands with mol wts of 60 K, 75 K, and 140 K. The intensities of all three bands were reduced by low concentrations (0.9-9 nM) of oPL. Higher concentrations of oGH abolished the 75 K and 140 K bands but reduced the intensity of the 60 K band by only 20-30%. oPRL had minimal effect on band intensities. These observations suggest the presence of two functionally and structurally distinct receptors in pregnant liver: the oPL receptor, which has high affinity for oPL and low affinity for oGH and oPRL.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

为了确定胎盘催乳素(PL)和生长激素(GH)的结合位点之间是否存在结构差异,我们比较了[125I]羊(o)PL和[125I]oGH与妊娠中期和晚期的胎儿及妊娠绵羊以及出生后3天至7个月的非妊娠绵羊肝脏膜共价交联形成的复合物的分子量。早在妊娠中期就检测到胎儿肝脏中有特异性的[125I]oPL结合位点,[125I]oPL与胎儿肝脏膜的交联产生了一条主要的放射带,分子量为60±5K(平均值±标准差)。低浓度(0.9 - 9 nM)的未标记oPL能特异性地与[125I]oPL竞争结合60K复合物。相比之下,oGH和oPRL仅在高得多的浓度(≥90 nM)下才竞争结合60K复合物。此外,未观察到[125I]oGH或[125I]oPRL与胎儿肝脏膜的特异性交联。这些发现表明羊胎儿肝脏中存在一个独特的PL结合位点。由于oPL的分子量为22K,oPL受体蛋白的估计分子量为38±5K。出生后的第一周,[125I]oGH结合位点的数量显著增加。[125I]oGH与出生后肝脏的交联产生了表观分子量为75K和140K的放射带。oPL、oGH和oPRL竞争结合75K和140K复合物的相对效力与这些激素竞争出生后肝脏中[125I]oGH结合位点的相对效力相似,这表明75K和140K条带代表与[125I]oGH共价结合的oGH受体亚基。[125I]oPL与妊娠和出生后非妊娠肝脏的交联产生了分子量为60K·75K和140K的三条放射带。低浓度(0.9 - 9 nM)的oPL降低了所有三条带的强度。较高浓度的oGH消除了75K和140K条带,但仅使60K条带的强度降低了20 - 30%。oPRL对条带强度的影响最小。这些观察结果表明妊娠肝脏中存在两种功能和结构不同的受体:oPL受体,它对oPL具有高亲和力,对oGH和oPRL具有低亲和力。(摘要截短于400字)

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