Suitability of Various Membrane Lipophilic Probes for the Detection of Trogocytosis by Flow Cytometry

被引:22
作者
Daubeuf, Sandrine [1 ,2 ]
Bordier, Christine [1 ,2 ]
Hudrisier, Denis [1 ,2 ]
Joly, Etienne [1 ,2 ]
机构
[1] IPBS, CNRS, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, IPBS, F-31077 Toulouse, France
关键词
trogocytosis; immunomonitoring; immune response; lymphocyte; TRAP assay; membrane probes; fluorescent lipophilic probes; T-CELLS; COMPLEXES; CAPTURE; PEPTIDE; ASSAY; APC;
D O I
10.1002/cyto.a.20679
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Trogocytosis is a recently discovered phenomenon whereby lymphocytes capture fragments of the plasma membrane from antigen presenting cells (APCs). Using APCs labeled with widely used fluorescent lipophilic probes, we previously described a trogocytosis analysis protocol (TRAP) useful to understand the mechanisms and biological consequences of this process and to identify lymphocytes reacting specifically with antigen-bearing APCs. We have compared the suitability of 22 different fluorescent lipophilic probes for use in TRAP assays with cytotoxic T lymphocytes (CTL). The criteria we used were: simple and efficient incorporation in APC membranes, minimal passive diffusion among cells but efficient transfer onto T cells during trogocytosis. Sphingosin-based probes were found to incorporate inefficiently into cells. For others with unsaturated lipid chains, we found a tendency for extensive passive diffusion. In the end, about a third of the probes tested were found to be suitable in TRAP assays, which an carry either C16 or C18 saturated carbon chains, including some that can be excited with a red laser. Moreover, we found it possible to combine TRAP assays based on lipophilic probes with intracellular cytokine detection. We have identified a set of new lipophilic fluorescent probes suitable for TRAP assays in combination with intracellular staining. (c) 2008 International Society for Advancement of cytometry
引用
收藏
页码:380 / 389
页数:10
相关论文
共 18 条
[1]   Phenotypic analysis of antigen-specific T lymphocytes [J].
Altman, JD ;
Moss, PAH ;
Goulder, PJR ;
Barouch, DH ;
McHeyzerWilliams, MG ;
Bell, JI ;
McMichael, AJ ;
Davis, MM .
SCIENCE, 1996, 274 (5284) :94-96
[2]   Quantifying viable virus-specific T cells without a priori knowledge of fine epitope specificity [J].
Beadling, Carol ;
Slifka, Mark K. .
NATURE MEDICINE, 2006, 12 (10) :1208-1212
[3]  
Brezinschek RI, 1999, J IMMUNOL, V162, P1677
[4]   A live-cell assay to detect antigen-specific CD4+ T cells with diverse cytokine profiles [J].
Chattopadhyay, PK ;
Yu, J ;
Roederer, M .
NATURE MEDICINE, 2005, 11 (10) :1113-1117
[5]  
Daubeuf Sandrine, 2007, Immunol Invest, V36, P687, DOI 10.1080/08820130701674596
[6]   A simple trogocytosis-based method to detect, quantify, characterize and purify antigen-specific live lymphocytes by flow cytometry, via their capture of membrane fragments from antigen-presenting cells [J].
Daubeuf, Sandrine ;
Puaux, Anne-Laure ;
Joly, Etienne ;
Hudrisier, Denis .
NATURE PROTOCOLS, 2006, 1 (06) :2536-2542
[7]   Intercellular transfer of cell-surface proteins is common and can affect many stages of an immune response [J].
Davis, Daniel M. .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (03) :238-243
[8]   T-CELL RECEPTOR ANTAGONIST PEPTIDES INDUCE POSITIVE SELECTION [J].
HOGQUIST, KA ;
JAMESON, SC ;
HEATH, WR ;
HOWARD, JL ;
BEVAN, MJ ;
CARBONE, FR .
CELL, 1994, 76 (01) :17-27
[9]   Cutting edge: CTLs rapidly capture membrane fragments from target cells in a TCR signaling-dependent manner [J].
Hudrisier, D ;
Riond, J ;
Mazarguil, H ;
Gairin, JE ;
Joly, E .
JOURNAL OF IMMUNOLOGY, 2001, 166 (06) :3645-3649
[10]   What is trogocytosis and what is its purpose? [J].
Joly, E ;
Hudrisier, D .
NATURE IMMUNOLOGY, 2003, 4 (09) :815-815