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干扰素-γ与培养的人胎肺表面活性剂成分的合成

Interferon-gamma and synthesis of surfactant components by cultured human fetal lung.

作者信息

Ballard P L, Liley H G, Gonzales L W, Odom M W, Ammann A J, Benson B, White R T, Williams M C

机构信息

Department of Pediatrics and Anatomy, University of California, San Francisco 94143.

出版信息

Am J Respir Cell Mol Biol. 1990 Feb;2(2):137-43. doi: 10.1165/ajrcmb/2.2.137.

Abstract

We examined the effects of interferon-gamma (IFN-gamma) on development of the surfactant system in alveolar epithelial cells of fetal lung. Explants of second-trimester human fetal lung were cultured for 1 to 6 days in serum-free medium containing recombinant human IFN-gamma (0.03 to 30 ng/ml) and/or dexamethasone (10 or 100 nM). Treatment for 3 days with IFN-gamma alone, dexamethasone alone, and IFN plus dexamethasone increased the content of surfactant protein A (SP-A, 28 to 36 kD) by approximately 3-, 2.5-, and 10-fold, respectively. The biphasic response pattern of SP-A to dexamethasone (stimulation initially and inhibition with continued culture) was not altered by the presence of IFN-gamma. IFN-gamma also stimulated accumulation of SP-A mRNA (2.7-fold at 24 h) but did not affect the levels of mRNAs for surfactant protein B (18 kD) and surfactant protein C (5 kD). To assess the effect of IFN-gamma on synthesis of surfactant lipids, we determined the content of phosphatidylcholine, the rate of labeled choline incorporation into phosphatidylcholine, saturation of newly synthesized phosphatidylcholine, and the activity of fatty acid synthetase, a glucocorticoid-inducible enzyme. Treatment of explants for 5 days with IFN-gamma had no effect on these parameters. Studies by light and electron microscopy revealed little difference between control and IFN-treated explants with regard to cell viability and epithelial cell differentiation. We conclude that IFN-gamma has a selective stimulatory effect on SP-A among surfactant components.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了γ干扰素(IFN-γ)对胎儿肺脏肺泡上皮细胞表面活性物质系统发育的影响。将孕中期人胎儿肺脏外植体在含有重组人IFN-γ(0.03至30 ng/ml)和/或地塞米松(10或100 nM)的无血清培养基中培养1至6天。单独用IFN-γ、单独用地塞米松以及IFN加地塞米松处理3天,分别使表面活性蛋白A(SP-A,28至36 kD)的含量增加了约3倍、2.5倍和10倍。IFN-γ的存在并未改变SP-A对地塞米松的双相反应模式(最初刺激,持续培养则抑制)。IFN-γ还刺激了SP-A mRNA的积累(24小时时增加2.7倍),但不影响表面活性蛋白B(18 kD)和表面活性蛋白C(5 kD)的mRNA水平。为评估IFN-γ对表面活性脂质合成的影响,我们测定了磷脂酰胆碱的含量、标记胆碱掺入磷脂酰胆碱的速率、新合成磷脂酰胆碱的饱和度以及脂肪酸合成酶(一种糖皮质激素诱导酶)的活性。用IFN-γ处理外植体5天对这些参数没有影响。光镜和电镜研究显示,对照和经IFN处理的外植体在细胞活力和上皮细胞分化方面几乎没有差异。我们得出结论,IFN-γ对表面活性物质成分中的SP-A具有选择性刺激作用。(摘要截短至250字)

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