Quantitative colocalization analysis of multicolor confocal immunofluorescence microscopy images: Pushing pixels to explore biological phenomena

被引:346
作者
Zinchuk, Vadim [1 ]
Zinchuk, Olga [2 ]
Okada, Teruhiko [1 ]
机构
[1] Kochi Univ, Fac Med, Dept Anat & Cell Biol, Nanko Ku, Kochi 7838505, Japan
[2] Kochi Univ, Fac Med, Dept Ophthalmol, Nanko Ku, Kochi 7838505, Japan
关键词
confocal fluorescence microscopy; quantitative colocalization analysis; colocalization coefficients; colocalization software;
D O I
10.1267/ahc.07002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Quantitative colocalization analysis is an advanced digital imaging tool to examine antigens of interest in immunofluorescence images obtained using confocal microscopes. It employs specialized algorithms to estimate the degree of overlap of fluorescence signals and thus enables acquiring important new information not otherwise obtainable using qualitative approaches alone. As raw confocal images have high levels of background, they should be prepared to become suitable for reliable calculation of colocalization coefficients by correcting it. We provide concise theoretical basis of quantitative colocalization analysis, discuss its limitations, and describe proper use of the technique. The use of quantitative colocalization analysis is demonstrated by studying bile salt export pump and multidrug resistance associated protein 2 in the liver and major basic protein and platelet activating factor receptor antigens in conjunctiva. The review is focused on the applicability and correct interpretation of the results of colocalization coefficients calculations.
引用
收藏
页码:101 / 111
页数:11
相关论文
共 35 条
[1]   New methods to evaluate colocalization of fluorophores in immunocytochemical preparations as exemplified by a study on A2A and D2 receptors in Chinese hamster ovary cells [J].
Agnati, LF ;
Fuxe, K ;
Torvinen, M ;
Genedani, S ;
Franco, R ;
Watson, S ;
Nussdorfer, GG ;
Leo, G ;
Guidolin, D .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2005, 53 (08) :941-953
[2]   Trypsin-sensitive modulation of intestinal epithelial MD-2 as mechanism of lipopolysaccharide tolerance [J].
Cario, Elke ;
Golenbock, Douglas T. ;
Visintin, Alberto ;
Ruenzi, Michael ;
Gerken, Guido ;
Podolsky, Daniel K. .
JOURNAL OF IMMUNOLOGY, 2006, 176 (07) :4258-4266
[3]   SIMULTANEOUS CONFOCAL RECORDING OF MULTIPLE FLUORESCENT LABELS WITH IMPROVED CHANNEL SEPARATION [J].
CARLSSON, K ;
ASLUND, N ;
MOSSBERG, K ;
PHILIP, J .
JOURNAL OF MICROSCOPY-OXFORD, 1994, 176 :287-299
[4]   IMPROVED FLUOROPHORE SEPARATION WITH IMS CONFOCAL MICROSCOPY [J].
CARLSSON, K ;
ULFHAKE, B .
NEUROREPORT, 1995, 6 (08) :1169-1173
[5]  
*COLOCALIZATION RE, 2006, COLOCALIZER PRO US G
[6]  
Costes SV, 2004, BIOPHYS J, V86, P3993, DOI 10.1529/biophysi.103.038422
[7]   Tumor metastasis but not tumor growth is dependent on Src-mediated vascular permeability [J].
Criscuoli, ML ;
Nguyen, M ;
Eliceiri, BP .
BLOOD, 2005, 105 (04) :1508-1514
[8]  
DEMANDOLX D, 1995, J TRACE MICROPROBE T, V13, P217
[9]   Multicolour analysis and local image correlation in confocal microscopy [J].
Demandolx, D ;
Davoust, J .
JOURNAL OF MICROSCOPY, 1997, 185 :21-36
[10]   How the molecule number is correctly quantified in two-color fluorescence cross-correlation spectroscopy:: Corrections for cross-talk and quenching in experiments [J].
Földes-Papp, Z .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2005, 6 (06) :437-444