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甲胎蛋白抑制巨噬细胞Ia抗原的表达。

Alpha-fetoprotein inhibits macrophage expression of Ia antigens.

作者信息

Lu C Y, Changelian P S, Unanue E R

出版信息

J Immunol. 1984 Apr;132(4):1722-7.

PMID:6199409
Abstract

Murine alpha-fetoprotein (AFP) is a major protein in amnionic fluid and perinatal sera. AFP has been postulated to contribute to the immunologic hyporesponsiveness of the fetus and neonate, as well as protecting the fetus from rejection by the mother. We now report that AFP acts in vitro to inhibit macrophage expression of cell surface Ia antigens, the class II glycoproteins of the major histocompatibility gene complex. In culture, macrophages incubated with a T cell lymphokine developed Ia as detected by either immunofluorescence or a cell radioimmunoassay. Both mouse amnionic fluid and AFP inhibited the expression of Ia in a dose-dependent manner. Five preparations of AFP derived from three sources--day-old neonates, amnionic fluid, and a hepatoma cell line--were effective. The concentration of AFP that inhibited by 50% the expression of Ia was about 10(-6) M. Mouse amnionic fluid and AFP did not affect the viability of the macrophage nor was the surface expression of H-2K and C3 receptors affected. The inhibitory effect of AFP did not depend on the presence of T cells in the culture. AFP did not appear to inhibit the direct interaction of lymphokine with macrophages; AFP did inhibit if given days after a pulse of lymphokine. The concentrations of prostaglandins carried by AFP were insignificant and could not explain the inhibitory effects.

摘要

小鼠甲胎蛋白(AFP)是羊水和围产期血清中的一种主要蛋白质。据推测,AFP有助于胎儿和新生儿的免疫低反应性,同时保护胎儿免受母体的排斥。我们现在报告,AFP在体外可抑制巨噬细胞表面Ia抗原的表达,Ia抗原是主要组织相容性基因复合体的II类糖蛋白。在培养中,用T细胞淋巴因子孵育的巨噬细胞,通过免疫荧光或细胞放射免疫测定法可检测到Ia的产生。小鼠羊水和AFP均以剂量依赖方式抑制Ia的表达。来自三种来源(新生一天的新生儿、羊水和肝癌细胞系)的五种AFP制剂均有效。抑制50% Ia表达的AFP浓度约为10^(-6) M。小鼠羊水和AFP不影响巨噬细胞的活力,也不影响H-2K和C3受体的表面表达。AFP的抑制作用不依赖于培养物中T细胞的存在。AFP似乎不抑制淋巴因子与巨噬细胞的直接相互作用;如果在淋巴因子脉冲后数天给予AFP,则有抑制作用。AFP携带的前列腺素浓度微不足道,无法解释其抑制作用。

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