• 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
Calcium is required for the expression of anthrax lethal toxin activity in the macrophagelike cell line J774A.1.在巨噬细胞样细胞系J774A.1中,炭疽致死毒素活性的表达需要钙。
Infect Immun. 1989 Jul;57(7):2107-14. doi: 10.1128/iai.57.7.2107-2114.1989.
2
Protein synthesis is required for expression of anthrax lethal toxin cytotoxicity.炭疽致死毒素细胞毒性的表达需要蛋白质合成。
Infect Immun. 1994 Jul;62(7):2958-62. doi: 10.1128/iai.62.7.2958-2962.1994.
3
Internalization and processing of Bacillus anthracis lethal toxin by toxin-sensitive and -resistant cells.
J Biol Chem. 1989 Jul 5;264(19):11099-102.
4
Cytotoxicity of anthrax lethal factor microinjected into macrophage cells through Sendai virus envelopes.通过仙台病毒包膜微注射到巨噬细胞中的炭疽致死因子的细胞毒性。
Indian J Biochem Biophys. 1997 Feb-Apr;34(1-2):186-91.
5
Intracellular calcium antagonist protects cultured peritoneal macrophages against anthrax lethal toxin-induced cytotoxicity.
Cell Biol Toxicol. 2000;16(2):137-44. doi: 10.1023/a:1007646227674.
6
Monoclonal antibodies directed against protective antigen of Bacillus anthracis enhance lethal toxin activity in vivo.针对炭疽芽孢杆菌保护性抗原的单克隆抗体在体内增强致死毒素活性。
FEMS Immunol Med Microbiol. 2011 Jun;62(1):11-22. doi: 10.1111/j.1574-695X.2011.00782.x. Epub 2011 Feb 2.
7
In vitro and in vivo characterization of anthrax anti-protective antigen and anti-lethal factor monoclonal antibodies after passive transfer in a mouse lethal toxin challenge model to define correlates of immunity.在小鼠致死毒素攻击模型中进行被动转移后,对炭疽抗保护性抗原和抗致死因子单克隆抗体进行体外和体内特性分析,以确定免疫相关性。
Infect Immun. 2007 Nov;75(11):5443-52. doi: 10.1128/IAI.00529-07. Epub 2007 Aug 20.
8
Dehydroepiandrosterone and melatonin prevent Bacillus anthracis lethal toxin-induced TNF production in macrophages.脱氢表雄酮和褪黑素可预防炭疽杆菌致死毒素诱导巨噬细胞产生肿瘤坏死因子。
Cell Biol Toxicol. 2000;16(3):165-74. doi: 10.1023/a:1007606921569.
9
Effect of nasal immunization with protective antigen of Bacillus anthracis on protective immune response against anthrax toxin.用炭疽芽孢杆菌保护性抗原进行鼻腔免疫对炭疽毒素保护性免疫反应的影响。
Vaccine. 2002 Jun 21;20(21-22):2836-9. doi: 10.1016/s0264-410x(02)00207-4.
10
Serum protease cleavage of Bacillus anthracis protective antigen.炭疽芽孢杆菌保护性抗原的血清蛋白酶裂解
J Gen Microbiol. 1992 Mar;138(3):543-9. doi: 10.1099/00221287-138-3-543.

引用本文的文献

1
The Importance of Therapeutically Targeting the Binary Toxin from .靶向. 二元毒素治疗的重要性
Int J Mol Sci. 2021 Mar 13;22(6):2926. doi: 10.3390/ijms22062926.
2
Structure of the cell-binding component of the binary toxin reveals a di-heptamer macromolecular assembly.二元毒素细胞结合组件的结构揭示了一个二七聚体的大分子组装体。
Proc Natl Acad Sci U S A. 2020 Jan 14;117(2):1049-1058. doi: 10.1073/pnas.1919490117. Epub 2020 Jan 2.
3
A Membrane Potential- and Calpain-Dependent Reversal of Caspase-1 Inhibition Regulates Canonical NLRP3 Inflammasome.一种依赖于膜电位和钙蛋白酶的半胱天冬酶-1 抑制逆转调节经典的 NLRP3 炎症小体。
Cell Rep. 2018 Aug 28;24(9):2356-2369.e5. doi: 10.1016/j.celrep.2018.07.098.
4
A Biologically-Based Computational Approach to Drug Repurposing for Anthrax Infection.一种基于生物学的炭疽感染药物再利用计算方法。
Toxins (Basel). 2017 Mar 10;9(3):99. doi: 10.3390/toxins9030099.
5
Cellular adaptation to anthrax lethal toxin-induced mitochondrial cholesterol enrichment, hyperpolarization, and reactive oxygen species generation through downregulating MLN64 in macrophages.细胞通过下调巨噬细胞中的 MLN64 适应炭疽致死毒素诱导的线粒体胆固醇蓄积、超极化和活性氧生成。
Mol Cell Biol. 2012 Dec;32(23):4846-60. doi: 10.1128/MCB.00494-12. Epub 2012 Oct 1.
6
Constitutive MEK1 activation rescues anthrax lethal toxin-induced vascular effects in vivo.组成型 MEK1 激活可挽救体内炭疽致死毒素诱导的血管效应。
Infect Immun. 2010 Dec;78(12):5043-53. doi: 10.1128/IAI.00604-10. Epub 2010 Sep 20.
7
Cellular and systemic effects of anthrax lethal toxin and edema toxin.炭疽致死毒素和水肿毒素的细胞和全身效应。
Mol Aspects Med. 2009 Dec;30(6):439-55. doi: 10.1016/j.mam.2009.07.003. Epub 2009 Jul 26.
8
Anthrax lethal toxin and Salmonella elicit the common cell death pathway of caspase-1-dependent pyroptosis via distinct mechanisms.炭疽致死毒素和沙门氏菌通过不同机制引发依赖半胱天冬酶-1的细胞焦亡这一共同细胞死亡途径。
Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4312-7. doi: 10.1073/pnas.0707370105. Epub 2008 Mar 12.
9
Anthrax lethal factor represses glucocorticoid and progesterone receptor activity.炭疽致死因子可抑制糖皮质激素和孕激素受体活性。
Proc Natl Acad Sci U S A. 2003 May 13;100(10):5706-11. doi: 10.1073/pnas.1036973100. Epub 2003 Apr 30.
10
Anthrax edema toxin requires influx of calcium for inducing cyclic AMP toxicity in target cells.炭疽水肿毒素在靶细胞中诱导环磷酸腺苷毒性需要钙离子内流。
Infect Immun. 2002 Sep;70(9):4997-5007. doi: 10.1128/IAI.70.9.4997-5007.2002.

本文引用的文献

1
Biologically active phorbol esters specifically alter affinity of epidermal growth factor membrane receptors.生物活性佛波醇酯特异性改变表皮生长因子膜受体的亲和力。
Nature. 1979 May 31;279(5712):387-91. doi: 10.1038/279387a0.
2
The entry of diphtheria toxin into the mammalian cell cytoplasm: evidence for lysosomal involvement.白喉毒素进入哺乳动物细胞质:溶酶体参与的证据。
J Cell Biol. 1980 Dec;87(3 Pt 1):849-54. doi: 10.1083/jcb.87.3.849.
3
Intracellular study of ionic events underlying intestinal membrane transport of oligopeptides.寡肽肠道膜转运离子事件的细胞内研究。
Nature. 1980 Sep 11;287(5778):157-8. doi: 10.1038/287157a0.
4
Effect of membrane potential on Na+-dependent sugar transport by ATP-depleted intestinal cells.膜电位对ATP耗竭的肠细胞中Na⁺依赖性糖转运的影响。
Am J Physiol. 1980 Mar;238(3):C73-80. doi: 10.1152/ajpcell.1980.238.3.C73.
5
The effect of Ca2+ and the trifluoperazine on the processing of human acetylated low density lipoprotein by non-parenchymal liver cells.
FEBS Lett. 1981 Sep 14;132(1):61-6. doi: 10.1016/0014-5793(81)80427-9.
6
The role of calcium in cell death.钙在细胞死亡中的作用。
Life Sci. 1981 Sep 28;29(13):1289-95. doi: 10.1016/0024-3205(81)90670-6.
7
Role of coated vesicles, microfilaments, and calmodulin in receptor-mediated endocytosis by cultured B lymphoblastoid cells.包被小泡、微丝和钙调蛋白在培养的B淋巴母细胞受体介导的内吞作用中的作用。
J Cell Biol. 1980 Oct;87(1):132-41. doi: 10.1083/jcb.87.1.132.
8
Characterization of binding of the Ca++ channel antagonist, [3H]nitrendipine, to guinea-pig ileal smooth muscle.钙离子通道拮抗剂[3H]尼群地平与豚鼠回肠平滑肌结合的特性研究
J Pharmacol Exp Ther. 1983 May;225(2):291-309.
9
Entry of the toxic proteins abrin, modeccin, ricin, and diphtheria toxin into cells. I. Requirement for calcium.毒性蛋白相思子毒素、毒蛋白、蓖麻毒素和白喉毒素进入细胞的过程。I. 对钙的需求。
J Biol Chem. 1982 Jul 10;257(13):7495-503.
10
Essential role of calcium in cellular internalization of Pseudomonas toxin.钙在铜绿假单胞菌毒素细胞内化中的重要作用。
Infect Immun. 1982 Feb;35(2):715-20. doi: 10.1128/iai.35.2.715-720.1982.

在巨噬细胞样细胞系J774A.1中,炭疽致死毒素活性的表达需要钙。

Calcium is required for the expression of anthrax lethal toxin activity in the macrophagelike cell line J774A.1.

作者信息

Bhatnagar R, Singh Y, Leppla S H, Friedlander A M

机构信息

United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland 21701-5011.

出版信息

Infect Immun. 1989 Jul;57(7):2107-14. doi: 10.1128/iai.57.7.2107-2114.1989.

DOI:10.1128/iai.57.7.2107-2114.1989
PMID:2499545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC313848/
Abstract

Anthrax lethal toxin, which consists of two separate proteins, protective antigen (Mr, 82,700) and lethal factor (Mr, approximately 83,000), is cytotoxic to the macrophagelike cell line J774A.1. Removal of calcium from the culture medium protected cells against the action of lethal toxin. Calcium depletion during the binding phase of intoxication afforded only partial protection. Further analysis showed that calcium removal caused some inhibition of protective antigen binding but that it had minimal effect on proteolytic conversion of protective antigen to the active 63-kilodalton fragment and that it had no effect on lethal factor binding. Cells to which lethal toxin had bound in the presence of calcium were protected when transferred to calcium-depleted culture medium, indicating a role for calcium at a postbinding stage. When ammonium chloride is present with lethal toxin, toxin accumulates in intracellular vesicles. Calcium-free medium protected these cells upon removal of the amine block, suggesting that calcium is also required at a step after internalization of lethal toxin. Calcium channel blockers inhibited 45Ca2+ uptake and protected cells against cytotoxicity. Calmodulin inhibitors also protected against the action of lethal toxin, suggesting involvement of calmodulin at a step during intoxication. We conclude that calcium is required at several steps in the intoxication of cells by anthrax lethal toxin.

摘要

炭疽致死毒素由两种独立的蛋白质组成,即保护性抗原(分子量82,700)和致死因子(分子量约83,000),对巨噬细胞样细胞系J774A.1具有细胞毒性。从培养基中去除钙可保护细胞免受致死毒素的作用。中毒结合阶段的钙耗竭仅提供部分保护。进一步分析表明,去除钙会对保护性抗原的结合产生一定抑制,但对保护性抗原蛋白水解转化为活性63千道尔顿片段的影响最小,且对致死因子的结合没有影响。在存在钙的情况下与致死毒素结合的细胞,转移至无钙培养基中时受到保护,这表明钙在结合后阶段起作用。当氯化铵与致死毒素同时存在时,毒素会在细胞内囊泡中积累。去除胺阻断后,无钙培养基可保护这些细胞,这表明在致死毒素内化后的某个步骤也需要钙。钙通道阻滞剂抑制45Ca2+摄取并保护细胞免受细胞毒性。钙调蛋白抑制剂也可保护细胞免受致死毒素的作用,这表明钙调蛋白在中毒过程中的某个步骤发挥作用。我们得出结论,炭疽致死毒素使细胞中毒的几个步骤都需要钙。