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叙利亚仓鼠胚胎发育过程中干扰素系统的发育调控表达。

Developmentally regulated expression of the interferon system during Syrian hamster embryogenesis.

作者信息

Greene J J, Dyer R H, Yang L C, Ts'o P O

出版信息

J Interferon Res. 1984 Fall;4(4):517-27. doi: 10.1089/jir.1984.4.517.

Abstract

Expression of interferon (IFN) during embryogenesis of the Syrian hamster has been characterized with respect to (1) the antiviral activity to IFN; (2) the activity of the IFN-induced enzyme, 2',5'-oligo A synthetase; (3) the subpopulation of IFN producing cells, and (4) the molecular structure of the elaborated IFN. These components of the IFN system were examined in cell cultures derived from embryos excised at 8-13 days of gestation and determined as a function of both in utero gestation and in vitro passaging. The antiviral responsiveness of nine-day gestation cultures (9 dgc) was 1/4-1/6 of that of 13 dgc, but in vitro passaging increased the responsiveness as did in vivo development. IFN enhancement of the synthetase level in 9 dgc was only minimal when compared with that in 13 dgc. However, the 9 dgc contained an unusually high basal level of the enzyme. During in vivo development and in vitro passaging, the basal levels of the enzymes progressively declined while the IFN-induced levels progressively increased. IFN production in embryo cells following induction by Newcastle disease virus differs substantially, depending on the gestational age of the cells. Using an agarose-overlay "zone of protection" assay, 8 dgc were found to contain 10-12 times the number of cells producing zones of protection than 13 dgc. Passaging of 9 dgc cells reduced the number of zones to the level of the 13 dgc, but had no effect on 13 dgc. Chromatographic analysis of IFN produced by 9 dgc and 13 dgc revealed the presence of an additional, unique species of "embryonic" IFN in 9 dgc which was not observed in IFN from 13 dgc. These observations suggest that the expression of various components of the IFN system are under developmental control during embryogenesis.

摘要

叙利亚仓鼠胚胎发育过程中干扰素(IFN)的表达已在以下几个方面得到表征:(1)IFN的抗病毒活性;(2)IFN诱导酶2',5'-寡腺苷酸合成酶的活性;(3)产生IFN的细胞亚群;(4)所产生的IFN的分子结构。在妊娠8 - 13天切除的胚胎来源的细胞培养物中检查了IFN系统的这些组成部分,并确定其是子宫内妊娠和体外传代的函数。九天妊娠培养物(9 dgc)的抗病毒反应性是13 dgc的1/4 - 1/6,但体外传代增加了反应性,体内发育也有同样效果。与13 dgc相比,9 dgc中合成酶水平的IFN增强作用仅很微小。然而,9 dgc中该酶的基础水平异常高。在体内发育和体外传代过程中,酶的基础水平逐渐下降,而IFN诱导水平逐渐增加。新城疫病毒诱导后胚胎细胞中IFN的产生根据细胞的胎龄有很大差异。使用琼脂糖覆盖“保护区”测定法,发现8 dgc中产生保护区的细胞数量是13 dgc的10 - 12倍。9 dgc细胞传代后保护区数量降至13 dgc的水平,但对13 dgc没有影响。对9 dgc和13 dgc产生的IFN进行色谱分析发现,9 dgc中存在一种额外的、独特的“胚胎”IFN,而在13 dgc的IFN中未观察到。这些观察结果表明,IFN系统的各种组成部分的表达在胚胎发育过程中受发育控制。

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