母猴和胎猴血清中胰岛素样生长因子(IGF)轴的特征。

Growth regulation Pub Date : 1995-12-01
A F Tarantal, S E Gargosky
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引用次数: 0

摘要

胰岛素样生长因子(IGFs)是受血清载体蛋白(IGF结合蛋白[igfbp])调控的胎儿生长发育的关键影响因子。研究评估了igf和igfbp在猕猴中的发育特征,猕猴是人类发育和疾病的重要非人类灵长类动物模型。研究了igf - 1、igf - 2和IGFBP-3在恒河猴(Macaca mulatta)和长尾猴(Macaca fascicularis)妊娠中晚期胎儿和坝体中的表达情况。从孕90 ~ 160天和出生后1个月,通过心脏穿刺每10天采集一次胎儿血液;在相似的时间点采集母体血液样本。结果表明,母体血清IGF-I和IGF-II没有显著变化,而胎儿血清IGF-I和IGF-II浓度在妊娠中期至晚期增加了约两倍。在两个物种之间没有发现显著差异。western -配体印迹分析显示,母体和胎儿室中主要存在45-40 (IGFBP-3)和28 kDa (IGFBP-1)的igfbp,而使用IGFBP-3特异性抗血清的western -免疫印迹分析显示45-40和28 kDa的免疫反应形式。因此,尽管IGF-I、IGF-II和IGFBP-3在妊娠期间在母体血清中相对不受影响,但胎儿的IGF-I、IGF-II和IGFBP-3浓度在与人类胎儿相似的发育过程中增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of the insulin-like growth factor (IGF) axis in the serum of maternal and fetal macaques (Macaca mulatta and Macaca fascicularis).

The insulin-like growth factors (IGFs) are key effectors of fetal growth and development which are modulated by serum carrier proteins (IGF binding proteins [IGFBPs]). Studies were performed to evaluate the developmental profile of IGFs and IGFBPs in the macaque, an important nonhuman primate model for human development and disease. IGF-I, IGF-II, and IGFBP-3 were studied in the rhesus (Macaca mulatta) and long-tailed (Macaca fascicularis) monkey fetus and dam during the second and third trimesters of pregnancy. Serial fetal blood samples were collected by cardiocentesis every 10 days from gestational day (GD) 90-160, and at 1 month postnatal age; maternal blood samples were collected at similar timepoints. Results indicated that maternal sera IGF-I and IGF-II did not change significantly whereas fetal concentrations of serum IGF-I and IGF-II increased approximately two-fold during the second to the third trimesters. No significant differences were detected between the two species. Western-ligand blot analysis revealed predominant IGFBPs of 45-40 (IGFBP-3) and 28 kDa (IGFBP-1) in both the maternal and fetal compartments, and Western-immunoblot analysis using a specific antisera against IGFBP-3 indicated 45-40 and 28 kDa immunoreactive forms. Thus, although IGF-I, IGF-II, and IGFBP-3 remained relatively unaffected in maternal sera during this period of gestation, fetal concentrations of IGF-I, IGF-II, and IGFBP-3 increased in a developmental profile similar to the human fetus.

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