• 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

一种使用流式细胞术的荧光自然杀伤细胞检测法。

A fluorescence NK assay using flow cytometry.

作者信息

McGinnes K, Chapman G, Marks R, Penny R

出版信息

J Immunol Methods. 1986 Jan 22;86(1):7-15. doi: 10.1016/0022-1759(86)90258-9.

DOI:10.1016/0022-1759(86)90258-9
PMID:3944470
Abstract

A flow cytometric NK assay was developed in which the K562 targets were labelled with the fluorogenic substrate, carboxyfluorescein diacetate (c'FDA). This new assay compared favourably with results obtained using the conventional 51Cr-release assay. c'FDA was not toxic to target cells and did not inhibit lysis. The assay permits the evaluation of various aspects of NK activity such as the activity of NK-enriched, IFN-alpha-activated, and ALG-inhibited populations. The assay can be used in place of 51Cr-release, and has the advantages of being able to directly monitor target cell lysis of reducing overall assay time, and the avoidance of radioisotope usage.

摘要

开发了一种流式细胞术NK检测方法,其中用荧光底物羧基荧光素二乙酸酯(c'FDA)标记K562靶细胞。这种新检测方法与使用传统的51Cr释放检测方法得到的结果相比具有优势。c'FDA对靶细胞无毒且不抑制裂解。该检测方法能够评估NK活性的各个方面,如NK富集群体、IFN-α激活群体和ALG抑制群体的活性。该检测方法可替代51Cr释放检测方法,具有能够直接监测靶细胞裂解、减少总体检测时间以及避免使用放射性同位素的优点。

相似文献

1
A fluorescence NK assay using flow cytometry.一种使用流式细胞术的荧光自然杀伤细胞检测法。
J Immunol Methods. 1986 Jan 22;86(1):7-15. doi: 10.1016/0022-1759(86)90258-9.
2
Optimization of cytotoxic assay by target cell retention of the fluorescent dye carboxyfluorescein diacetate (CFDA) and comparison with conventional 51CR release assay.通过荧光染料羧基荧光素二乙酸酯(CFDA)的靶细胞保留优化细胞毒性测定并与传统的51Cr释放测定进行比较。
J Immunol Methods. 1992 Oct 19;155(1):19-24. doi: 10.1016/0022-1759(92)90266-v.
3
Comparison of fluorochrome-labeled and 51Cr-labeled targets for natural killer cytotoxicity assay.用于自然杀伤细胞细胞毒性分析的荧光染料标记靶标与51铬标记靶标的比较。
J Immunol Methods. 1989 Aug 15;122(1):15-24. doi: 10.1016/0022-1759(89)90329-3.
4
An improved flow cytometry-based natural killer cytotoxicity assay involving calcein AM staining of effector cells.一种改进的基于流式细胞术的自然杀伤细胞细胞毒性检测方法,该方法涉及对效应细胞进行钙黄绿素 AM 染色。
Ann Clin Lab Sci. 2012 Winter;42(1):42-9.
5
The application of flow cytometry in the study of natural killer cell cytotoxicity.
Clin Immunol Immunopathol. 1987 Dec;45(3):356-65. doi: 10.1016/0090-1229(87)90088-2.
6
A novel method for the simultaneous assessment of natural killer cell conjugate formation and cytotoxicity at the single-cell level by multi-parameter flow cytometry.一种通过多参数流式细胞术在单细胞水平同时评估自然杀伤细胞共轭体形成和细胞毒性的新方法。
J Immunol Methods. 2000 May 26;239(1-2):35-44. doi: 10.1016/s0022-1759(00)00161-7.
7
Abnormal macrophages and NK cell cytotoxicity in human systemic lupus erythematosus and the role of interferon and serum factors.人类系统性红斑狼疮中异常巨噬细胞和自然杀伤细胞的细胞毒性以及干扰素和血清因子的作用
Acta Virol. 1989 Sep;33(5):447-53.
8
A novel multiparametric flow cytometry-based cytotoxicity assay simultaneously immunophenotypes effector cells: comparisons to a 4 h 51Cr-release assay.一种基于新型多参数流式细胞术的细胞毒性检测方法可同时对效应细胞进行免疫表型分析:与4小时51铬释放检测法的比较。
J Immunol Methods. 2007 Aug 31;325(1-2):51-66. doi: 10.1016/j.jim.2007.05.013. Epub 2007 Jun 28.
9
A versatile flow cytometry-based assay for the determination of short- and long-term natural killer cell activity.
J Immunol Methods. 1995 Sep 25;185(2):209-16. doi: 10.1016/0022-1759(95)00116-r.
10
Assessment of human natural killer and lymphokine-activated killer cell cytotoxicity against Toxoplasma gondii trophozoites and brain cysts.评估人类自然杀伤细胞和淋巴因子激活的杀伤细胞对刚地弓形虫滋养体和脑囊肿的细胞毒性。
J Immunol. 1989 Oct 15;143(8):2684-91.

引用本文的文献

1
Analysis of the mechanisms regulating soluble PD-1 production and function in human NK cells.分析调节人 NK 细胞可溶性 PD-1 产生和功能的机制。
Front Immunol. 2023 Aug 10;14:1229341. doi: 10.3389/fimmu.2023.1229341. eCollection 2023.
2
IL-1R8 silencing improves the anti-tumor function of freshly isolated human NK cells.IL-1R8 沉默可增强新鲜分离的人 NK 细胞的抗肿瘤功能。
J Immunother Cancer. 2022 Mar;10(3). doi: 10.1136/jitc-2021-003858.
3
T1D progression is associated with loss of CD3CD56 regulatory T cells that control CD8 T cell effector functions.
1 型糖尿病的进展与调节性 T 细胞(CD3CD56)的缺失有关,这些细胞可控制 CD8 T 细胞的效应功能。
Nat Metab. 2020 Feb;2(2):142-152. doi: 10.1038/s42255-020-0173-1. Epub 2020 Feb 17.
4
Human CAR NK Cells: A New Non-viral Method Allowing High Efficient Transfection and Strong Tumor Cell Killing.人细胞毒性自然杀伤细胞:一种新型非病毒方法,可实现高效转染和强烈杀伤肿瘤细胞。
Front Immunol. 2019 Apr 30;10:957. doi: 10.3389/fimmu.2019.00957. eCollection 2019.
5
NK cells control breast cancer and related cancer stem cell hematological spread.自然杀伤细胞控制乳腺癌及相关癌症干细胞的血液扩散。
Oncoimmunology. 2017 Feb 23;6(3):e1284718. doi: 10.1080/2162402X.2017.1284718. eCollection 2017.
6
Application of an improved flow cytometry-based NK cell activity assay in adult hemophagocytic lymphohistiocytosis.一种改进的基于流式细胞术的自然杀伤细胞活性检测方法在成人噬血细胞性淋巴组织细胞增生症中的应用
Int J Hematol. 2017 Jun;105(6):828-834. doi: 10.1007/s12185-017-2195-3. Epub 2017 Feb 9.
7
Mechanical stress downregulates MHC class I expression on human cancer cell membrane.机械应力下调人癌细胞表面 MHC Ⅰ类分子的表达。
PLoS One. 2014 Dec 26;9(12):e111758. doi: 10.1371/journal.pone.0111758. eCollection 2014.
8
Early hematopoietic zinc finger protein prevents tumor cell recognition by natural killer cells.早期造血锌指蛋白可阻止自然杀伤细胞识别肿瘤细胞。
J Immunol. 2009 Apr 15;182(8):4529-37. doi: 10.4049/jimmunol.0802109.
9
Contact-dependent stimulation and inhibition of dendritic cells by natural killer cells.自然杀伤细胞对树突状细胞的接触依赖性刺激与抑制
J Exp Med. 2002 Feb 4;195(3):335-41. doi: 10.1084/jem.20010934.
10
Cytotoxicity of unstimulated and thrombin-activated platelets to human tumour cells.未刺激和凝血酶激活的血小板对人肿瘤细胞的细胞毒性。
Immunology. 1993 Apr;78(4):650-6.