• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Rabbit macrophage interferons. II. Some physicochemical properties and estimations of molecular weights.兔巨噬细胞干扰素。II. 一些物理化学性质及分子量测定
J Exp Med. 1967 Apr 1;125(4):579-93. doi: 10.1084/jem.125.4.579.
2
Rabbit macrophage interferons. I. Conditions for biosynthesis by virus-infected and uninfected cells.兔巨噬细胞干扰素。I. 病毒感染和未感染细胞的生物合成条件。
J Exp Med. 1967 Apr 1;125(4):559-77. doi: 10.1084/jem.125.4.559.
3
Characterization of virus- and endotoxin-induced interferons obtained from the serum and urine of rabbits.从兔血清和尿液中获得的病毒和内毒素诱导干扰素的特性
J Virol. 1967 Oct;1(5):883-90. doi: 10.1128/JVI.1.5.883-890.1967.
4
Analysis of the interferons induced in mice in vivo and in macrophages in vitro by Newcastle disease virus and by polyinosinic-polycytidylic acid.新城疫病毒和聚肌苷酸-聚胞苷酸在体内诱导小鼠及体外诱导巨噬细胞产生干扰素的分析。
J Interferon Res. 1986 Feb;6(1):21-8. doi: 10.1089/jir.1986.6.21.
5
Role of interferon-like viral inhibitor in endotoxin-induced corneal resistance to Newcastle disease virus.干扰素样病毒抑制剂在内毒素诱导的角膜对新城疫病毒抗性中的作用。
J Bacteriol. 1966 Jan;91(1):251-6. doi: 10.1128/jb.91.1.251-256.1966.
6
Inhibition of macrophage migration by virus-induced interferon preparations.病毒诱导的干扰素制剂对巨噬细胞迁移的抑制作用。
Jpn J Microbiol. 1975 Oct;19(5):337-42. doi: 10.1111/j.1348-0421.1975.tb00889.x.
7
STUDIES ON PERSISTENT INFECTIONS OF TISSUE CULTURES. V. THE INITIAL STAGES OF INFECTION OF L(MCN) CELLS BY NEWCASTLE DISEASE VIRUS.组织培养持续性感染的研究。V. 新城疫病毒对L(MCN)细胞的初始感染阶段
J Exp Med. 1964 Jan 1;119(6):895-921. doi: 10.1084/jem.119.6.895.
8
Interferon induced by endotoxin and Newcastle disease virus in rabbit macrophage and kidney cell cultures.内毒素和新城疫病毒在兔巨噬细胞和肾细胞培养物中诱导产生的干扰素。
Proc Soc Exp Biol Med. 1973 Feb;142(2):481-6. doi: 10.3181/00379727-142-37050.
9
[Role of macrophages in interferon production in mice (author's transl)].巨噬细胞在小鼠干扰素产生中的作用(作者译)
Ann Immunol (Paris). 1979 Jul-Aug;130C(4):581-6.
10
Differences in mouse interferons according to cell source and mode of induction.根据细胞来源和诱导方式的小鼠干扰素差异。
Infect Immun. 1977 Sep;17(3):572-9. doi: 10.1128/iai.17.3.572-579.1977.

引用本文的文献

1
Spontaneous production of human interferon.人干扰素的自发产生
Proc Natl Acad Sci U S A. 1980 Oct;77(10):5938-42. doi: 10.1073/pnas.77.10.5938.
2
Characterization of virus- and endotoxin-induced interferons obtained from the serum and urine of rabbits.从兔血清和尿液中获得的病毒和内毒素诱导干扰素的特性
J Virol. 1967 Oct;1(5):883-90. doi: 10.1128/JVI.1.5.883-890.1967.
3
[Physico-chemical properties of myxovirus-induced serum interferons of the rabbit].[黏液病毒诱导的兔血清干扰素的物理化学性质]
Arch Gesamte Virusforsch. 1969;28(1):51-62.
4
Interferon synthesis in x-irradiated animals. IV. Donor-type serum interferons in rat-to-mouse radiation chimeras injected with Newcastle disease virus.X射线照射动物体内的干扰素合成。IV. 注射新城疫病毒的大鼠-小鼠辐射嵌合体中的供体型血清干扰素。
Proc Natl Acad Sci U S A. 1969 Jul;63(3):732-9. doi: 10.1073/pnas.63.3.732.
5
Interferon--1968. How much do we understand?干扰素——1968年。我们了解多少?
Calif Med. 1968 Jul;109(1):24-34.
6
[Gel chromatography of virus-induced interferon from exudate granulocytes].[来自渗出性粒细胞的病毒诱导干扰素的凝胶色谱分析]
Arch Gesamte Virusforsch. 1973;40(1):128-31.
7
Further study of spontaneous interferon produced by hamster peritoneal cells.对仓鼠腹膜细胞产生的自发性干扰素的进一步研究。
Arch Gesamte Virusforsch. 1972;38(2):149-58. doi: 10.1007/BF01249665.
8
N,N-dioctadecyl-N',N'-bis(2-hydroxyethyl) propanediamine: antiviral activity and interferon stimulation in mice.N,N-二辛基-N',N'-双(2-羟乙基)丙二胺:小鼠体内的抗病毒活性及干扰素刺激作用
Antimicrob Agents Chemother. 1973 Apr;3(4):498-502. doi: 10.1128/AAC.3.4.498.
9
Heterogeneity of rabbit serum interferon induced by poly I:C.聚肌胞诱导的兔血清干扰素的异质性
Arch Gesamte Virusforsch. 1974;44(1):51-7. doi: 10.1007/BF01242180.
10
[Cellular origin or rabbit serum interferon induced by Newcastle disease virus].[新城疫病毒诱导的兔血清干扰素的细胞起源]
Arch Gesamte Virusforsch. 1973;40(3):334-40.

本文引用的文献

1
Interferon-like virus-inhibitor induced in human leukocytes by phytohemagglutinin.植物血凝素在人白细胞中诱导产生的类干扰素病毒抑制剂。
Science. 1965 Jul 16;149(3681):310-1.
2
INTERFERON. A REVIEW AND ANALYSIS OF RECENT OBSERVATIONS.干扰素。近期观察结果的综述与分析。
Am J Med. 1965 May;38:726-37. doi: 10.1016/0002-9343(65)90193-2.
3
PHYSICAL PROPERTIES OF CHICK INTERFERON.鸡干扰素的物理特性
J Bacteriol. 1965 Feb;89(2):462-9. doi: 10.1128/jb.89.2.462-469.1965.
4
INTERFERON-LIKE VIRAL INHIBITOR IN RABBITS AFTER INTRAVENOUS ADMINISTRATION OF ENDOTOXIN.静脉注射内毒素后兔体内的类干扰素病毒抑制剂
Science. 1964 Dec 11;146(3650):1472-4. doi: 10.1126/science.146.3650.1472.
5
Studies on vaccinia virus plaque formation and its inhibition by interferon. III. A simplified plaque inhibition assay of interferon.痘苗病毒蚀斑形成及其受干扰素抑制的研究。III. 一种简化的干扰素蚀斑抑制试验。
Virology. 1963 Mar;19:302-9. doi: 10.1016/0042-6822(63)90068-0.
6
Interferon activity associated with high molecular weight proteins in the circulation of mice injected with endotoxin or bacteria.与注射内毒素或细菌的小鼠血液循环中高分子量蛋白质相关的干扰素活性。
Virology. 1965 Nov;27(3):429-31. doi: 10.1016/0042-6822(65)90124-8.
7
Heterogeneity of rabbit serum interferons.兔血清干扰素的异质性。
Nature. 1966 Jul 30;211(5048):541-2. doi: 10.1038/211541a0.
8
Rabbit macrophage interferons. I. Conditions for biosynthesis by virus-infected and uninfected cells.兔巨噬细胞干扰素。I. 病毒感染和未感染细胞的生物合成条件。
J Exp Med. 1967 Apr 1;125(4):559-77. doi: 10.1084/jem.125.4.559.
9
Estimation of the molecular weights of proteins by Sephadex gel-filtration.用葡聚糖凝胶过滤法估算蛋白质的分子量
Biochem J. 1964 May;91(2):222-33. doi: 10.1042/bj0910222.

兔巨噬细胞干扰素。II. 一些物理化学性质及分子量测定

Rabbit macrophage interferons. II. Some physicochemical properties and estimations of molecular weights.

作者信息

Smith T J, Wagner R R

出版信息

J Exp Med. 1967 Apr 1;125(4):579-93. doi: 10.1084/jem.125.4.579.

DOI:10.1084/jem.125.4.579
PMID:6066967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2138362/
Abstract

Antiviral factors present in cultures of rabbit peritoneal macrophages or rabbit kidney (RK) cells infected with Newcastle disease virus (NDV) and those in cultures of uninfected macrophages all fulfilled the biological and physicochemical criteria for classification as interferons. Virus-induced macrophage and RK interferons were slightly more stable to heat or acid than "spontaneously produced" or endotoxin-induced macrophage interferon. Interferon activity in serum of NDV-infected rabbits was decidedly more labile than NDV-induced macrophage interferon. However, these differences in lability were too slight to serve as a useful basis for distinguishing one rabbit interferon from another. Rabbit interferons from various sources could be differentiated by filtration through Sephadex G-100 and their molecular weights estimated by comparison with elution profiles of a series of marker proteins of known molecular weight. Each of four different preparations of rabbit interferons was found to contain more than one molecular component. Elution peaks for three NDV-induced interferons were equivalent to the following molecular weights: RK approximately 44,000-45,000 and > 134,000 (variable and < 1% when present); macrophage approximately 37,000, 44,000-45,000, and > 134,000 (variable and <1% when present); and serum approximately 50,000-52,000 and > 134,000 ( approximately 10% and heat labile). NDV-induced serum interferon may also contain another molecular component of mol wt approximately 45,000 represented by a trailing shoulder from the major 51,000 mol wt peak. Endotoxin-induced macrophage interferon proved to be polydisperse. Sephadex filtration of this interferon did not reveal clear and consistent elution patterns, partially owing to its low initial titer and lability. However, variable peaks of biological activity could be detected in Sephadex fractions equivalent to approximate molecular weight values of > 134,000, 72,000-78,000, 33,000-38,000, 28,000-30,000, and possibly a component of 42,000-45,000. A major component of mol wt approximately 37,000 was present in all samples of endotoxin-induced macrophage interferon. The other constituents may be biologically active subunits or polymers. These data indicate that rabbit macrophages produce two primary kinds of interferon: (a) an RK-like component of mol wt approximately 45,000 that is synthesized in greatest amount after viral induction, and (b) a different species of mol wt approximately 37,000 that can also be synthesized in the absence of viral induction. The presence of major interferon constituents of mol wt approximately 51,000 and > 134,000 in rabbit serum after viral induction suggests that macrophages are not the principal interferon-producing cells that respond to intravenous injection of NDV.

摘要

感染新城疫病毒(NDV)的兔腹膜巨噬细胞或兔肾(RK)细胞培养物中存在的抗病毒因子,以及未感染巨噬细胞培养物中的抗病毒因子,均符合作为干扰素分类的生物学和物理化学标准。病毒诱导的巨噬细胞和RK干扰素比“自发产生的”或内毒素诱导的巨噬细胞干扰素对热或酸的稳定性略高。感染NDV的兔血清中的干扰素活性比NDV诱导的巨噬细胞干扰素明显更不稳定。然而,这些稳定性的差异太小,无法作为区分一种兔干扰素与另一种兔干扰素的有用依据。来自各种来源的兔干扰素可以通过Sephadex G - 100过滤进行区分,并通过与一系列已知分子量的标记蛋白的洗脱图谱比较来估计其分子量。发现四种不同的兔干扰素制剂中的每一种都含有不止一种分子成分。三种NDV诱导的干扰素的洗脱峰相当于以下分子量:RK约为44,000 - 45,000和> 134,000(存在时可变且<1%);巨噬细胞约为37,000、44,000 - 45,000和> 134,000(存在时可变且<1%);血清约为50,000 - 52,000和> 134,000(约10%且对热不稳定)。NDV诱导的血清干扰素可能还含有另一种分子量约为45,000的分子成分,由主要的51,000分子量峰的拖尾峰表示。内毒素诱导的巨噬细胞干扰素被证明是多分散的。这种干扰素的Sephadex过滤未显示出清晰一致的洗脱模式,部分原因是其初始滴度低且不稳定。然而,在相当于分子量> 134,000、72,000 - 78,000、33,000 - 38,000、28,000 - 30,000以及可能42,000 - 45,000的Sephadex级分中可以检测到可变的生物活性峰。内毒素诱导的巨噬细胞干扰素的所有样品中都存在一种分子量约为37,000的主要成分。其他成分可能是生物活性亚基或聚合物。这些数据表明兔巨噬细胞产生两种主要类型的干扰素:(a)一种分子量约为45,000的类似RK的成分,在病毒诱导后合成量最大,以及(b)一种不同的分子量约为37,000的类型,在没有病毒诱导的情况下也可以合成。病毒诱导后兔血清中存在分子量约为51,000和> 134,000的主要干扰素成分,这表明巨噬细胞不是对静脉注射NDV作出反应的主要干扰素产生细胞。