• 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

补体基因表达的调控

Regulation of complement gene expression.

作者信息

Colten H R, Dowton S B

出版信息

Biochem Soc Symp. 1986;51:37-46.

PMID:3101700
Abstract

The availability of molecular probes for approximately half of the 20 known complement genes now permits a detailed examination of the regulation of complement expression in liver and at extrahepatic sites in tissue macrophages. Primary cell culture, cell lines and cells transfected with DNA bearing complement genes have been used in this analysis. Pretranslational regulation of complement production has been induced by well defined cytokines such as interleukin-1 and gamma-interferon, as well as directly by endotoxin. The effect of those agents on complement genes is tissue and species specific and is developmentally regulated. These data form the basis for the elucidation of the genomic structural requirements for regulation of inflammation and, by extension, specific immune responsiveness.

摘要

目前,针对20种已知补体基因中约一半的分子探针已可获取,这使得详细研究肝脏及组织巨噬细胞肝外部位补体表达的调控成为可能。原代细胞培养、细胞系以及用携带补体基因的DNA转染的细胞已用于此项分析。补体产生的翻译前调控已由明确的细胞因子如白细胞介素-1和γ-干扰素诱导产生,也可由内毒素直接诱导。这些因子对补体基因的作用具有组织和物种特异性,且受发育调控。这些数据为阐明炎症调控以及由此延伸的特异性免疫反应性的基因组结构要求奠定了基础。

相似文献

1
Regulation of complement gene expression.补体基因表达的调控
Biochem Soc Symp. 1986;51:37-46.
2
Constitutive and IL 1-regulated murine complement gene expression is strain and tissue specific.组成型和白细胞介素1调节的小鼠补体基因表达具有品系和组织特异性。
J Immunol. 1987 Feb 1;138(3):856-60.
3
Genetics of complement.补体的遗传学
Curr Top Hematol. 1980;3:111-74.
4
Effect of histamine on the gene expression and biosynthesis of complement components C2, factor B and C3 in mouse peritoneal macrophages.组胺对小鼠腹腔巨噬细胞中补体成分C2、B因子和C3基因表达及生物合成的影响。
Immunology. 1987 Apr;60(4):547-51.
5
Tissue-specific pretranslational regulation of complement production in human mononuclear phagocytes.人类单核吞噬细胞中补体产生的组织特异性转录前调控。
J Immunol. 1985 Apr;134(4):2610-6.
6
Ordering of genes for HLA antigens and complement components on the human 6th chromosome.人类第6号染色体上HLA抗原和补体成分的基因排序。
Prog Clin Biol Res. 1977;16:9-20.
7
Regulation of complement protein biosynthesis in mononuclear phagocytes.单核吞噬细胞中补体蛋白生物合成的调节
Ciba Found Symp. 1986;118:141-54. doi: 10.1002/9780470720998.ch10.
8
Molecular regulation of MHC class III (C4 and factor B) gene expression in mouse peritoneal macrophages.小鼠腹腔巨噬细胞中MHC III类(C4和B因子)基因表达的分子调控
J Immunol. 1984 Sep;133(3):1618-26.
9
Complement polymorphism, the major histocompatibility complex and associated diseases: a speculation.补体多态性、主要组织相容性复合体及相关疾病:一种推测
Mol Biol Med. 1983 Jul;1(1):161-8.
10
[B, C2 and C4 complement factors, the HLA system and diseases. Genetic relation].[B、C2和C4补体因子、HLA系统与疾病。遗传关系]
Pathol Biol (Paris). 1983 Sep;31(7):622-30.

引用本文的文献

1
Gene expression in periodontal tissues following treatment.治疗后牙周组织中的基因表达。
BMC Med Genomics. 2008 Jul 7;1:30. doi: 10.1186/1755-8794-1-30.
2
Human major histocompatibility complex contains a new cluster of genes between the HLA-D and complement C4 loci.人类主要组织相容性复合体在HLA - D和补体C4基因座之间包含一个新的基因簇。
Nucleic Acids Res. 1990 Dec 25;18(24):7251-7. doi: 10.1093/nar/18.24.7251.