Imaging Flow Cytometry: Coping with Heterogeneity in Biological Systems

被引:127
作者
Barteneva, Natasha S. [1 ,2 ,3 ]
Fasler-Kan, Elizaveta [4 ]
Vorobjev, Ivan A. [5 ,6 ]
机构
[1] Childrens Hosp Boston, Immune Dis Inst, Boston, MA 02115 USA
[2] Childrens Hosp Boston, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Harvard Univ, Dept Pediat, Sch Med, Boston, MA 02115 USA
[4] Univ Appl Sci NW Switzerland FHNW, Inst Chem & Bioanalyt, Muttenz, Switzerland
[5] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow, Russia
[6] Moscow MV Lomonosov State Univ, Dept Cell Biol & Histol, Fac Biol, Moscow, Russia
关键词
imaging flow cytometry; flow cytometry; biological heterogeneity; fluorescence; cellular morphology; Poisson distribution; single cell; high-throughput fluorescent microscopy; LASER-SCANNING CYTOMETRY; SINGLE-CELL; GENE-EXPRESSION; STEM-CELLS; IMAGESTREAM CYTOMETRY; SIGNALING NETWORKS; FALSE POSITIVES; APOPTOSIS; BLOOD; PHOSPHORYLATION;
D O I
10.1369/0022155412453052
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Imaging flow cytometry (IFC) platforms combine features of flow cytometry and fluorescent microscopy with advances in data-processing algorithms. IFC allows multiparametric fluorescent and morphological analysis of thousands of cellular events and has the unique capability of identifying collected events by their real images. IFC allows the analysis of heterogeneous cell populations, where one of the cellular components has low expression (<0.03%) and can be described by Poisson distribution. With the help of IFC, one can address a critical question of statistical analysis of subcellular distribution of proteins in a cell. Here the authors review advantages of IFC in comparison with more traditional technologies, such as Western blotting and flow cytometry (FC), as well as new high-throughput fluorescent microscopy (HTFM), and discuss further developments of this novel analytical technique. (J Histochem Cytochem 60:723-733, 2012)
引用
收藏
页码:723 / 733
页数:11
相关论文
共 97 条
[1]   Numbers matter: Quantitative and dynamic analysis of the formation of an immunological synapse using imaging flow cytometry [J].
Ahmed, Fariyal ;
Friend, Sherree ;
George, Thaddeus C. ;
Barteneva, Natasha ;
Lieberman, Judy .
JOURNAL OF IMMUNOLOGICAL METHODS, 2009, 347 (1-2) :79-86
[2]   Platelet-leukocyte mixed conjugates in patients with atrial fibrillation [J].
Alberti, Silvia ;
Angeloni, Giulia ;
Tamburrelli, Chiara ;
Pampuch, Agnieszka ;
Izzi, Benedetta ;
Messano, Loredana ;
Parisi, Quintino ;
Santamaria, Matteo ;
Donati, Maria Benedetta ;
De Gaetano, Giovanni ;
Cerletti, Chiara .
PLATELETS, 2009, 20 (04) :235-241
[3]   INSITU END-LABELING DETECTS DNA STRAND BREAKS IN APOPTOSIS AND OTHER PHYSIOLOGICAL AND PATHOLOGICAL STATES [J].
ANSARI, B ;
COATES, PJ ;
GREENSTEIN, BD ;
HALL, PA .
JOURNAL OF PATHOLOGY, 1993, 170 (01) :1-8
[4]   Cutting edge:: FADD is not required for antigen receptor-mediated NF-κB activation [J].
Arechiga, AF ;
Bell, BD ;
Solomon, JC ;
Chu, IH ;
Dubois, CL ;
Hall, BE ;
George, TC ;
Coder, DM ;
Walsh, CM .
JOURNAL OF IMMUNOLOGY, 2005, 175 (12) :7800-7804
[5]   The role of PI3K/AKT, MAPK/ERK and NFκβ signalling in the maintenance of human embryonic stem cell pluripotency and viability highlighted by transcriptional profiling and functional analysis [J].
Armstrong, Lyle ;
Hughes, Owen ;
Yung, Sun ;
Hyslop, Louise ;
Stewart, Rebecca ;
Wappler, Ilka ;
Peters, Heiko ;
Walter, Theresia ;
Stojkovic, Petra ;
Evans, Jerome ;
Stojkovic, Miodrag ;
Lako, Majlinda .
HUMAN MOLECULAR GENETICS, 2006, 15 (11) :1894-1913
[6]   Cellular image analysis and imaging by flow cytometry [J].
Basiji, David A. ;
Ortyn, William E. ;
Liang, Luchuan ;
Venkatachalam, Vidya ;
Morrissey, Philip .
CLINICS IN LABORATORY MEDICINE, 2007, 27 (03) :653-+
[7]  
Bedner E, 1998, CYTOMETRY, V33, P47, DOI 10.1002/(SICI)1097-0320(19980901)33:1<47::AID-CYTO6>3.0.CO
[8]  
2-8
[9]  
Bedner E, 1999, CYTOMETRY, V35, P181, DOI 10.1002/(SICI)1097-0320(19990301)35:3<181::AID-CYTO1>3.0.CO
[10]  
2-5