• 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

Khellin, but not 8-methoxypsoralen, inhibits adenylyl cyclase system in HeLa cells.

作者信息

Di Stefano A, Trabalzini L, La Gaetana R, Parente L, Lusini P, Martelli P

机构信息

Department of Molecular Biology, University of Siena, Italy.

出版信息

Biochim Biophys Acta. 1995 Nov 9;1269(2):162-6. doi: 10.1016/0167-4889(95)00115-9.

DOI:10.1016/0167-4889(95)00115-9
PMID:7488649
Abstract

Until recently, the therapeutic effects of furocoumarins and furochromones plus UV-A light were thought to be due to their ability to form photoadducts with DNA in the cell nuclei; now it appears that membrane effector systems may be involved as targets. Here we show that in HeLa cells khellin at 1 and 5 microM final concentration, in combination with UV-A light, inhibits NaF-stimulated adenylyl cyclase activity and Pertussis Toxin (PT)-catalyzed ADP-ribosylation of alpha-subunits of inhibitory guanine nucleotide regulatory proteins (Gi) and increases GTPase activity. In the same experimental conditions, 8-methoxypsoralen (8-MOP), either alone or plus UV-A, does not affect adenylyl cyclase and GTPase activities. Our results suggest that in HeLa cells, through an interaction with a receptor and the mediation of Gi proteins, the adenylyl cyclase system is a target for khellin but not for 8-MOP.

摘要

相似文献

1
Khellin, but not 8-methoxypsoralen, inhibits adenylyl cyclase system in HeLa cells.
Biochim Biophys Acta. 1995 Nov 9;1269(2):162-6. doi: 10.1016/0167-4889(95)00115-9.
2
Pertussis toxin reverses the inhibition of the adenylyl cyclase system by khellin in HeLa cells.百日咳毒素可逆转凯林对HeLa细胞中腺苷酸环化酶系统的抑制作用。
Biochim Biophys Acta. 1996 Nov 8;1314(1-2):105-8. doi: 10.1016/s0167-4889(96)00084-5.
3
Determination of G-protein levels, ADP-ribosylation by cholera and pertussis toxins and the regulation of adenylyl cyclase activity in liver plasma membranes from lean and genetically diabetic (db/db) mice.测定瘦型和遗传性糖尿病(db/db)小鼠肝细胞膜中G蛋白水平、霍乱毒素和百日咳毒素介导的ADP核糖基化作用以及腺苷酸环化酶活性的调节。
Biochim Biophys Acta. 1991 Oct 21;1097(3):193-204. doi: 10.1016/0925-4439(91)90035-8.
4
Opioid inhibition of adenylyl cyclase in membranes from pertussis toxin-treated NG108-15 cells.阿片类物质对经百日咳毒素处理的NG108-15细胞的细胞膜中腺苷酸环化酶的抑制作用。
J Recept Signal Transduct Res. 1998 Jan;18(1):25-49. doi: 10.3109/10799899809039163.
5
Pertussis toxin-catalyzed ADP-ribosylation of adenylate cyclase. Effects of guanyl nucleotides and rhodopsin.百日咳毒素催化的腺苷酸环化酶的ADP-核糖基化。鸟苷核苷酸和视紫红质的作用。
Dev Biol Stand. 1985;61:43-9.
6
Pertussis toxin-mediated ADP-ribosylation of rabbit luteal Gi uncouples enkephalin inhibition of adenylyl cyclase.百日咳毒素介导的兔黄体Gi的ADP核糖基化作用使脑啡肽对腺苷酸环化酶的抑制作用解偶联。
Int J Biochem. 1990;22(1):31-7. doi: 10.1016/0020-711x(90)90074-d.
7
Inhibition of catalytic unit of adenylate cyclase and activation of GTPase of Ni protein by beta gamma-subunits of GTP-binding proteins.
FEBS Lett. 1986 Jun 23;202(1):63-8. doi: 10.1016/0014-5793(86)80650-0.
8
Site of pertussis toxin-induced ADP-ribosylation on Gi is critical for receptor modulation of GDP interaction with Gi.百日咳毒素诱导的Gi上ADP核糖基化的位点对于受体调节GDP与Gi的相互作用至关重要。
Mol Endocrinol. 1989 Feb;3(2):315-24. doi: 10.1210/mend-3-2-315.
9
Studies on nucleotide and receptor regulation of Gi proteins: effects of pertussis toxin.Gi蛋白的核苷酸和受体调节研究:百日咳毒素的作用
Mol Endocrinol. 1989 Jul;3(7):1115-24. doi: 10.1210/mend-3-7-1115.
10
Characterization of GTP-binding proteins coupled to inhibition of adenylyl cyclase in guinea pig tracheal epithelial cells.豚鼠气管上皮细胞中与腺苷酸环化酶抑制偶联的GTP结合蛋白的特性分析。
Am J Respir Cell Mol Biol. 1994 Jun;10(6):665-72. doi: 10.1165/ajrcmb.10.6.8003343.

引用本文的文献

1
A pathway to next-generation mast cell stabilizers identified through the novel Phytomedical Analytics for Research Optimization at Scale data platform.通过新型大规模研究优化植物医学分析数据平台确定的下一代肥大细胞稳定剂途径。
bioRxiv. 2025 Sep 4:2025.08.30.673232. doi: 10.1101/2025.08.30.673232.