• 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

流式细胞术对粒细胞进行多功能分析中的吞噬作用、细胞内pH值和细胞体积

Phagocytosis, intracellular pH, and cell volume in the multifunctional analysis of granulocytes by flow cytometry.

作者信息

Rothe G, Valet G

机构信息

Mildred-Scheel-Labor für Krebszellforschung, Max-Planck-Institut für Biochemie, Martinsried, Federal Republic of Germany.

出版信息

Cytometry. 1988 Jul;9(4):316-24. doi: 10.1002/cyto.990090408.

DOI:10.1002/cyto.990090408
PMID:2456897
Abstract

Phagocytosis of Escherichia coli K12 strain bacteria was used to measure by flow cytometry the functional activities of human granulocytes in whole blood or buffy coat preparations. In a first measurement, the increase in electric cell volume and acridine orange (AO) green and red fluorescence were used to quantify the degree of phagocytosis. In a second measurement, the intracellular pH and esterase activity of each cell were determined with 1,4-diacetoxy-2,3-dicyanobenzene to obtain information on the metabolic activities during phagocytosis and degradation of bacteria. The DNA of dead cells was simultaneously counterstained with propidium iodide in both assays. The volume, the AO green and red fluorescence, the internal pH, and esterase activity were automatically averaged for all granulocytes or lymphocytes of a measurement. The calculated mean values were transferred into the self-learning database of the DIAGNOS1-program system. The functional granulocyte parameters of normal healthy individuals can be used as reference values for the automated diagnosis of abnormal granulocytes in various infectious disease states. The assays require 1 ml of heparinized whole blood and the results are available within 1 hour.

摘要

利用大肠杆菌K12菌株细菌的吞噬作用,通过流式细胞术来测量全血或血沉棕黄层制剂中人类粒细胞的功能活性。在首次测量中,利用细胞电体积的增加以及吖啶橙(AO)的绿色和红色荧光来量化吞噬程度。在第二次测量中,用1,4 - 二乙酰氧基 - 2,3 - 二氰基苯测定每个细胞的细胞内pH值和酯酶活性,以获取有关细菌吞噬和降解过程中代谢活性的信息。在这两种测定中,死细胞的DNA同时用碘化丙啶进行复染。对一次测量中的所有粒细胞或淋巴细胞自动求体积、AO绿色和红色荧光、细胞内pH值以及酯酶活性的平均值。计算出的平均值被输入到DIAGNOS1程序系统的自学习数据库中。正常健康个体的功能性粒细胞参数可作为各种感染性疾病状态下异常粒细胞自动诊断的参考值。这些测定需要1毫升肝素化全血,结果在1小时内可得。

相似文献

1
Phagocytosis, intracellular pH, and cell volume in the multifunctional analysis of granulocytes by flow cytometry.流式细胞术对粒细胞进行多功能分析中的吞噬作用、细胞内pH值和细胞体积
Cytometry. 1988 Jul;9(4):316-24. doi: 10.1002/cyto.990090408.
2
Flow cytometric parameters of neutrophil function as early indicators of sepsis- or trauma-related pulmonary or cardiovascular organ failure.中性粒细胞功能的流式细胞术参数作为脓毒症或创伤相关肺或心血管器官衰竭的早期指标。
J Lab Clin Med. 1990 Jan;115(1):52-61.
3
Intracellular pH, esterase activity, and DNA measurements of human lung carcinomas by flow cytometry.通过流式细胞术对人肺癌进行细胞内pH值、酯酶活性及DNA测量。
Cytometry. 1990;11(3):341-8. doi: 10.1002/cyto.990110305.
4
Simultaneous measurement of phagocytosis and phagosomal pH by flow cytometry: role of polymorphonuclear neutrophilic leukocyte granules in phagosome acidification.通过流式细胞术同时测量吞噬作用和吞噬体pH值:多形核中性粒细胞颗粒在吞噬体酸化中的作用。
Cytometry. 1983 Nov;4(3):254-62. doi: 10.1002/cyto.990040311.
5
Kinetics of phagocytosis of Staphylococcus aureus and Escherichia coli by human granulocytes.人粒细胞对金黄色葡萄球菌和大肠杆菌的吞噬动力学
Immunology. 1979 Jun;37(2):453-65.
6
Neutrophil function is preserved in a pooled granulocyte component prepared from whole blood donations.从全血捐献制备的混合粒细胞成分中,中性粒细胞功能得以保留。
Br J Haematol. 2008 Mar;140(6):701-11. doi: 10.1111/j.1365-2141.2008.06996.x.
7
Flow-cytometric determination of intracellular pH, esterase activity and cell volume in human leukemic cell lines following in vitro incubation with cytostatic drugs.在体外与细胞抑制药物孵育后,通过流式细胞术测定人白血病细胞系中的细胞内pH值、酯酶活性和细胞体积。
Anal Cell Pathol. 1989 Dec;2(1):49-58.
8
Flow-cytometric characterization of stimulation, free radical formation, peroxidase activity and phagocytosis of human granulocytes with 2,7-dichlorofluorescein (DCF).用2,7-二氯荧光素(DCF)对人粒细胞的刺激、自由基形成、过氧化物酶活性和吞噬作用进行流式细胞术表征。
Eur J Cell Biol. 1987 Feb;43(1):128-33.
9
Use of SYTOX green dye in the flow cytometric analysis of bacterial phagocytosis.SYTOX绿染料在细菌吞噬作用流式细胞术分析中的应用。
Cytometry. 2002 Jun 1;48(2):93-6. doi: 10.1002/cyto.10107.
10
[An in vitro micromethod for studying phagocytic and bacteriocidal activity of granulocytes from peripheral blood].[一种用于研究外周血粒细胞吞噬和杀菌活性的体外微量方法]
Eksp Med Morfol. 1989;28(4):49-53.

引用本文的文献

1
Shifts in the fluorescence lifetime of EGFP during bacterial phagocytosis measured by phase-sensitive flow cytometry.通过相敏流动 cytometry 测量细菌吞噬过程中 EGFP 荧光寿命的变化。
Sci Rep. 2017 Jan 16;7:40341. doi: 10.1038/srep40341.
2
Phagocytosis and digestion of pH-sensitive fluorescent dye (Eos-FP) transfected E. coli in whole blood assays from patients with severe sepsis and septic shock.严重脓毒症和感染性休克患者全血试验中 pH 敏感荧光染料(Eos-FP)转染大肠杆菌的吞噬作用和消化。
J Cell Commun Signal. 2011 Jun;5(2):135-44. doi: 10.1007/s12079-010-0112-0. Epub 2011 Jan 12.
3
Applications of flow cytometry to clinical microbiology.
流式细胞术在临床微生物学中的应用。
Clin Microbiol Rev. 2000 Apr;13(2):167-95. doi: 10.1128/CMR.13.2.167.
4
Flow cytometric assay of phagocytic activity of human neutrophils and monocytes in whole blood by neutral red uptake.通过中性红摄取对全血中人类中性粒细胞和单核细胞的吞噬活性进行流式细胞术检测。
Ann Hematol. 1995 May;70(5):259-65. doi: 10.1007/BF01784045.
5
Flow cytometric approach to human polymorphonuclear leukocyte activation induced by gingival crevicular fluid in periodontal disease.流式细胞术检测牙周病龈沟液诱导的人多形核白细胞活化
Inflammation. 1995 Aug;19(4):479-87. doi: 10.1007/BF01534581.
6
Mechanisms of electrostimulated uptake of macromolecules into living cells.电刺激使大分子摄入活细胞的机制。
Naturwissenschaften. 1990 Nov;77(11):543-5. doi: 10.1007/BF01139269.
7
The adherence of endothelial cells to Dacron induces the expression of the intercellular adhesion molecule (ICAM-1).内皮细胞与涤纶的黏附会诱导细胞间黏附分子(ICAM-1)的表达。
Ann Surg. 1992 Nov;216(5):600-4. doi: 10.1097/00000658-199211000-00013.