• 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

补体如何杀死大肠杆菌。II. 致死事件明显的双打击性质。

How complement kills E. coli. II. The apparent two-hit nature of the lethal event.

作者信息

Wright S D, Levine R P

出版信息

J Immunol. 1981 Sep;127(3):1152-6.

PMID:7021676
Abstract

We have studied the nature of complement (C) action on red blood cells and E. coli with respect to the number of "hits" required for membrane damage. Our method of analysis involves adding various amounts of purified C7 or C8 to serum preparations immunochemically depleted of C7 or C8, respectively, in order to construct dose-response curves for the action of C's terminal complex. The shape of the dose-response curves reflects the single or multiple-hit nature of C action. Our method confirms that C acts on red cells by a 1-hit mechanism, whether measured by lysis or by the permeation of a small molecule. In contrast, we find with E. coli that C-mediated outer membrane damage, inner membrane damage, and killing all appear to require more than 1 hit. We have also discovered a property of E. coli that displays a nonlethal 1-hit response to C that is particularly useful in the analysis of multiple-hit dose-response curves. Simultaneous measurements of this single-hit phenomenon and the multiple-hit killing of E. coli allow us to make direct comparisons of the amount of C needed for each response. On the basis of the midpoints of the single and multiple-hit curves, C-mediated membrane damage and killing of E. coli appear to be a 2-hit process.

摘要

我们研究了补体(C)对红细胞和大肠杆菌的作用性质,涉及膜损伤所需的“命中”次数。我们的分析方法包括分别向免疫化学去除C7或C8的血清制剂中添加不同量的纯化C7或C8,以构建补体末端复合物作用的剂量反应曲线。剂量反应曲线的形状反映了补体作用的单次或多次命中性质。我们的方法证实,无论通过裂解还是小分子渗透来测量,补体对红细胞的作用都是通过单次命中机制。相比之下,我们发现对于大肠杆菌,补体介导的外膜损伤、内膜损伤和杀伤似乎都需要多次命中。我们还发现了大肠杆菌的一种特性,即对补体表现出非致死性的单次命中反应,这在多次命中剂量反应曲线的分析中特别有用。同时测量这种单次命中现象和大肠杆菌的多次命中杀伤,使我们能够直接比较每种反应所需的补体量。根据单次和多次命中曲线的中点,补体介导的大肠杆菌膜损伤和杀伤似乎是一个两次命中的过程。

相似文献

1
How complement kills E. coli. II. The apparent two-hit nature of the lethal event.补体如何杀死大肠杆菌。II. 致死事件明显的双打击性质。
J Immunol. 1981 Sep;127(3):1152-6.
2
How complement kills E. coli. I. Location of the lethal lesion.补体如何杀死大肠杆菌。I. 致死损伤的位置。
J Immunol. 1981 Sep;127(3):1146-51.
3
Complement-mediated inhibition of function in complement-resistant Escherichia coli.补体介导的对补体抗性大肠杆菌功能的抑制作用。
J Immunol. 1989 Mar 1;142(5):1591-5.
4
The deposition of C5b-9 complexes and its precursors on E. coli J5 during complement activation enhances uptake and toxicities of gentamicin.补体激活过程中C5b-9复合物及其前体在大肠杆菌J5上的沉积增强了庆大霉素的摄取和毒性。
Immunol Invest. 2008;37(3):245-61. doi: 10.1080/08820130801973682.
5
The attack phase of human complement: differentiation between membrane binding and complex formation by the detection of neoantigen expression in situ. A morphometric immunoferritin study.人类补体的攻击阶段:通过原位检测新抗原表达区分膜结合与复合物形成。一项形态计量免疫铁蛋白研究。
J Immunol. 1981 Sep;127(3):1089-93.
6
Moculating effect of the late-acting components of the complement system on the bactericidal activity of human polymorphonuclear leukocytes on E. coli 0111:B4.补体系统后期作用成分对人多形核白细胞针对大肠杆菌0111:B4的杀菌活性的影响
J Immunol. 1981 Nov;127(5):1910-5.
7
Protective effects of various compounds on lysis of antibody-coated sheep erythrocytes by hypotonic shock or complement.各种化合物对低渗休克或补体介导的抗体包被绵羊红细胞裂解的保护作用。
Methods Find Exp Clin Pharmacol. 1984 Jun;6(6):287-92.
8
Lysis of sheep red cells in neat autologous serum as a source of antibody and complement.以纯自身血清作为抗体和补体来源对绵羊红细胞进行裂解。
Acta Pathol Microbiol Immunol Scand Suppl. 1984;284:5-9.
9
Mapping of the complement C9 binding domain in paramyosin of the blood fluke Schistosoma mansoni.曼氏血吸虫副肌球蛋白中补体C9结合结构域的定位
Int J Parasitol. 2007 Jan;37(1):67-75. doi: 10.1016/j.ijpara.2006.09.011. Epub 2006 Oct 19.
10
Single-hit mechanism of tumour cell killing by radiation.辐射杀伤肿瘤细胞的单打击机制
Int J Radiat Biol. 2003 Feb;79(2):71-81.

引用本文的文献

1
bor gene of phage lambda, involved in serum resistance, encodes a widely conserved outer membrane lipoprotein.λ噬菌体的bor基因与血清抗性有关,编码一种广泛保守的外膜脂蛋白。
J Bacteriol. 1995 Mar;177(5):1247-53. doi: 10.1128/jb.177.5.1247-1253.1995.
2
Further characterization of complement resistance conferred on Escherichia coli by the plasmid genes traT of R100 and iss of ColV,I-K94.对R100的质粒基因traT和ColV、I-K94的iss赋予大肠杆菌的补体抗性进行进一步表征。
Infect Immun. 1982 Feb;35(2):654-9. doi: 10.1128/iai.35.2.654-659.1982.
3
Activation of complement by serum-resistant Neisseria gonorrhoeae. Assembly of the membrane attack complex without subsequent cell death.
血清抗性淋病奈瑟菌对补体的激活。膜攻击复合物的组装但随后细胞未死亡。
J Exp Med. 1982 Oct 1;156(4):1235-49. doi: 10.1084/jem.156.4.1235.
4
Serum sensitivity of a Pseudomonas aeruginosa mucoid strain.一株铜绿假单胞菌黏液型菌株的血清敏感性
Infect Immun. 1984 Sep;45(3):748-55. doi: 10.1128/iai.45.3.748-755.1984.
5
Is the membrane attack complex of complement an enzyme?补体的膜攻击复合物是一种酶吗?
Mol Cell Biochem. 1984;61(1):5-15. doi: 10.1007/BF00239603.
6
Serum resistance encoded by colicin V plasmids in Escherichia coli and its relationship to the plasmid transfer system.大肠杆菌中由大肠杆菌素V质粒编码的血清抗性及其与质粒转移系统的关系。
Infect Immun. 1984 Mar;43(3):947-53. doi: 10.1128/iai.43.3.947-953.1984.
7
Bactericidal and bacteriolytic activity of serum against gram-negative bacteria.血清对革兰氏阴性菌的杀菌和溶菌活性。
Microbiol Rev. 1983 Mar;47(1):46-83. doi: 10.1128/mr.47.1.46-83.1983.
8
Receptors for C3b and C3bi promote phagocytosis but not the release of toxic oxygen from human phagocytes.C3b和C3bi的受体促进吞噬作用,但不会促使人类吞噬细胞释放毒性氧。
J Exp Med. 1983 Dec 1;158(6):2016-23. doi: 10.1084/jem.158.6.2016.
9
Fibronectin and serum amyloid P component stimulate C3b- and C3bi-mediated phagocytosis in cultured human monocytes.纤连蛋白和血清淀粉样P成分可刺激培养的人单核细胞中由C3b和C3bi介导的吞噬作用。
J Exp Med. 1983 Oct 1;158(4):1338-43. doi: 10.1084/jem.158.4.1338.
10
Serum-resistant mutants of Escherichia coli O111 contain increased lipopolysaccharide, lack an O antigen-containing capsule, and cover more of their lipid A core with O antigen.大肠杆菌O111的血清抗性突变体含有增加的脂多糖,缺乏含O抗原的荚膜,并且其脂质A核心更多地被O抗原覆盖。
J Bacteriol. 1984 Sep;159(3):877-82. doi: 10.1128/jb.159.3.877-882.1984.