Transient Partial Permeabilization with Saponin Enables Cellular Barcoding Prior to Surface Marker Staining

被引:75
作者
Behbehani, Gregory K. [1 ,2 ,3 ]
Thom, Colin [4 ]
Zunder, Eli R. [1 ]
Finck, Rachel [1 ]
Gaudilliere, Brice [1 ,5 ]
Fragiadakis, Gabriela K. [1 ]
Fantl, Wendy J. [1 ]
Nolan, Garry P. [1 ]
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Baxter Lab Stem Cell Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Med, Sch Med, Div Hematol, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Med, Sch Med, Div Oncol, Stanford, CA 94305 USA
[4] Bozicevic Field & Francis LLP, Palo Alto, CA USA
[5] Stanford Univ, Sch Med, Dept Anesthesiol Perioperat & Pain Med, Stanford, CA 94305 USA
关键词
fluorescent cellular barcoding; mass-tag cellular barcoding; mass cytometry; permeabilization; saponin; MASS CYTOMETRY; FLOW-CYTOMETRY; ACTIVATION; IMMUNE; CELLS;
D O I
10.1002/cyto.a.22573
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescent cellular barcoding and mass-tag cellular barcoding are cytometric methods that enable high sample throughput, minimize inter-sample variation, and reduce reagent consumption. Previously employed barcoding protocols require that barcoding be performed after surface marker staining, complicating combining the technique with measurement of alcohol-sensitive surface epitopes. This report describes a method of barcoding fixed cells after a transient partial permeabilization with 0.02% saponin that results in efficient and consistent barcode staining with fluorescent or mass-tagged reagents while preserving surface marker staining. This approach simplifies barcoding protocols and allows direct comparison of surface marker staining of multiple samples without concern for variations in the antibody cocktail volume, antigen-antibody ratio, or machine sensitivity. Using this protocol, cellular barcoding can be used to reliably detect subtle differences in surface marker expression. (c) 2014 International Society for Advancement of Cytometry
引用
收藏
页码:1011 / 1019
页数:9
相关论文
共 25 条
[1]   viSNE enables visualization of high dimensional single-cell data and reveals phenotypic heterogeneity of leukemia [J].
Amir, El-ad David ;
Davis, Kara L. ;
Tadmor, Michelle D. ;
Simonds, Erin F. ;
Levine, Jacob H. ;
Bendall, Sean C. ;
Shenfeld, Daniel K. ;
Krishnaswamy, Smita ;
Nolan, Garry P. ;
Pe'er, Dana .
NATURE BIOTECHNOLOGY, 2013, 31 (06) :545-+
[2]   Single-cell mass cytometry adapted to measurements of the cell cycle [J].
Behbehani, Gregory K. ;
Bendall, Sean C. ;
Clutter, Matthew R. ;
Fantl, Wendy J. ;
Nolan, Garry P. .
CYTOMETRY PART A, 2012, 81A (07) :552-566
[3]   Single-Cell Mass Cytometry of Differential Immune and Drug Responses Across a Human Hematopoietic Continuum [J].
Bendall, Sean C. ;
Simonds, Erin F. ;
Qiu, Peng ;
Amir, El-ad D. ;
Krutzik, Peter O. ;
Finck, Rachel ;
Bruggner, Robert V. ;
Melamed, Rachel ;
Trejo, Angelica ;
Ornatsky, Olga I. ;
Balderas, Robert S. ;
Plevritis, Sylvia K. ;
Sachs, Karen ;
Pe'er, Dana ;
Tanner, Scott D. ;
Nolan, Garry P. .
SCIENCE, 2011, 332 (6030) :687-696
[4]   Multiplexed mass cytometry profiling of cellular states perturbed by small-molecule regulators [J].
Bodenmiller, Bernd ;
Zunder, Eli R. ;
Finck, Rachel ;
Chen, Tiffany J. ;
Savig, Erica S. ;
Bruggner, Robert V. ;
Simonds, Erin F. ;
Bendall, Sean C. ;
Sachs, Karen ;
Krutzik, Peter O. ;
Nolan, Garry P. .
NATURE BIOTECHNOLOGY, 2012, 30 (09) :858-U89
[5]   A Dual-Fluorescence High-Throughput Cell Line System for Probing Multidrug Resistance [J].
Brimacombe, Kyle R. ;
Hall, Matthew D. ;
Auld, Douglas S. ;
Inglese, James ;
Austin, Christopher P. ;
Gottesman, Michael M. ;
Fung, King-Leung .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2009, 7 (03) :233-249
[6]   Whole blood fixation and permeabilization protocol with red blood cell lysis for flow cytometry of intracellular phosphorylated epitopes in leukocyte subpopulations [J].
Chow, S ;
Hedley, D ;
Grom, P ;
Magari, R ;
Jacobberger, JW ;
Shankey, TV .
CYTOMETRY PART A, 2005, 67A (01) :4-17
[7]   A platinum-based covalent viability reagent for single-cell mass cytometry [J].
Fienberg, Harris G. ;
Simonds, Erin F. ;
Fantl, Wendy J. ;
Nolan, Garry P. ;
Bodenmiller, Bernd .
CYTOMETRY PART A, 2012, 81A (06) :467-475
[8]   Normalization of mass cytometry data with bead standards [J].
Finck, Rachel ;
Simonds, Erin F. ;
Jager, Astraea ;
Krishnaswamy, Smita ;
Sachs, Karen ;
Fantl, Wendy ;
Pe'er, Dana ;
Nolan, Garry P. ;
Bendall, Sean C. .
CYTOMETRY PART A, 2013, 83A (05) :483-+
[9]   Evaluation of calcineurin/NFAT inhibitor selectivity in primary human Th cells using bar-coding and phospho-flow cytometry [J].
Frischbutter, Stefan ;
Schultheis, Katherine ;
Paetzel, Michael ;
Radbruch, Andreas ;
Baumgrass, Ria .
CYTOMETRY PART A, 2012, 81A (11) :1005-1011
[10]   Guidelines on the use of multicolour flow cytometry in the diagnosis of haematological neoplasms [J].
Johansson, Ulrika ;
Bloxham, David ;
Couzens, Stephen ;
Jesson, Jennifer ;
Morilla, Ricardo ;
Erber, Wendy ;
Macey, Marion .
BRITISH JOURNAL OF HAEMATOLOGY, 2014, 165 (04) :455-488