• 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

通过51Cr释放试验评估细胞毒性。数学参数的生物学解释。

Cellular cytotoxicity assessed by the 51Cr release assay. Biological interpretation of mathematical parameters.

作者信息

Bol S J, Rosdorff H J, Ronteltap C P, Hennen L A

出版信息

J Immunol Methods. 1986 Jun 10;90(1):15-23. doi: 10.1016/0022-1759(86)90378-9.

DOI:10.1016/0022-1759(86)90378-9
PMID:3486921
Abstract

This study deals with the interpretation of primary data of the 51Cr release assay for cellular cytotoxicity. In particular the dose-effect relationship between increasing numbers of lymphoid cells and the percentage of target cells killed has been considered. The number of target cells killed depends on the frequency and the activity of cytotoxic cells. These two parameters are often not distinguished from each other, which causes confusion and frequently results in vague descriptions of cytotoxicity data. Because in many cases not all cells in the target cell population can be lysed, we recommend the introduction of the plateau value for target cell kill. This maximum of target cell kill is a measure of the frequency of lysable target cells, but also depends on the cytotoxic cell activity. Description of the dose-effect curve by y = A(1 - e-kx) allows the simultaneous calculation of the maximum kill (A) and the frequency of cytotoxic cells (k) in the lymphoid cell population (x). Results are presented which indicate that A and k represent totally independent biological parameters the use of which permits a more objective description of cytotoxicity data.

摘要

本研究涉及对用于细胞毒性的51Cr释放试验原始数据的解读。特别考虑了淋巴细胞数量增加与被杀伤靶细胞百分比之间的剂量效应关系。被杀伤的靶细胞数量取决于细胞毒性细胞的频率和活性。这两个参数常常未被区分开来,这会导致混淆并经常造成对细胞毒性数据的模糊描述。由于在许多情况下靶细胞群体中的所有细胞并非都能被裂解,我们建议引入靶细胞杀伤的平台值。这种靶细胞杀伤的最大值是可裂解靶细胞频率的一种度量,但也取决于细胞毒性细胞的活性。用y = A(1 - e-kx)描述剂量效应曲线,可同时计算淋巴细胞群体(x)中的最大杀伤值(A)和细胞毒性细胞的频率(k)。所呈现的结果表明,A和k代表完全独立的生物学参数,使用这些参数能够更客观地描述细胞毒性数据。

相似文献

1
Cellular cytotoxicity assessed by the 51Cr release assay. Biological interpretation of mathematical parameters.通过51Cr释放试验评估细胞毒性。数学参数的生物学解释。
J Immunol Methods. 1986 Jun 10;90(1):15-23. doi: 10.1016/0022-1759(86)90378-9.
2
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.
3
Assessment of immunological parameters during tumour development in a murine model.在小鼠模型肿瘤发生过程中免疫参数的评估。
Indian J Exp Biol. 1989 Jun;27(6):497-501.
4
Measurement of cytotoxicity by target cell release and retention of the fluorescent dye bis-carboxyethyl-carboxyfluorescein (BCECF).通过靶细胞释放和保留荧光染料双羧乙基羧基荧光素(BCECF)来测量细胞毒性。
J Immunol Methods. 1988 Apr 6;108(1-2):255-64. doi: 10.1016/0022-1759(88)90427-9.
5
An enzymatic assay for the detection of natural cytotoxicity.一种用于检测天然细胞毒性的酶活性测定法。
J Immunol Methods. 1980;35(1-2):83-90. doi: 10.1016/0022-1759(80)90152-0.
6
Measurement of natural killer cell cytotoxicity by area under a cytotoxic curve. A method suitable for rheumatoid arthritis.通过细胞毒性曲线下面积测量自然杀伤细胞的细胞毒性。一种适用于类风湿性关节炎的方法。
J Immunol Methods. 1988 Nov 25;115(1):95-8. doi: 10.1016/0022-1759(88)90314-6.
7
Natural cytotoxicity of human blood monocytes and natural killer cells and their cytotoxic factors: discriminating effects of actinomycin D.人血单核细胞和自然杀伤细胞的天然细胞毒性及其细胞毒性因子:放线菌素D的鉴别作用
Int J Cancer. 1985 May 15;35(5):691-9. doi: 10.1002/ijc.2910350519.
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 real-time digital bio-imaging system to quantify cellular cytotoxicity as an alternative to the standard chromium-51 release assay.一种用于量化细胞毒性的实时数字生物成像系统,作为标准铬-51释放试验的替代方法。
Immunology. 2017 Apr;150(4):489-494. doi: 10.1111/imm.12702. Epub 2017 Jan 19.
10
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.

引用本文的文献

1
Combination of lymphocyte number and function in evaluating host immunity.淋巴细胞数量与功能相结合在评估宿主免疫力中的应用。
Aging (Albany NY). 2019 Dec 20;11(24):12685-12707. doi: 10.18632/aging.102595.
2
Cell-mediated autophagy promotes cancer cell survival.细胞介导的自噬促进癌细胞存活。
Cancer Res. 2012 Jun 15;72(12):2970-9. doi: 10.1158/0008-5472.CAN-11-3396. Epub 2012 Apr 13.
3
Supplementation with selenium and human immune cell functions. II. Effect on cytotoxic lymphocytes and natural killer cells.
Biol Trace Elem Res. 1994 Apr-May;41(1-2):115-27. doi: 10.1007/BF02917222.