Correction of image instability in confocal microscopy using image realignment - Effects on the analysis of intracellular calcium

被引:0
作者
Massensini, AR
Romano-Silva, MA
Suckling, J
Gomez, MV
Brammer, MJ
机构
[1] Kings Coll London, Inst Psychiat, Dept Biostat & Comp, Brain Imaging Anal Unit, London SE5 8AF, England
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Fisiol & Biofis, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Farmacol, Belo Horizonte, MG, Brazil
基金
英国惠康基金;
关键词
image instability; confocal microscopy; image realignment;
D O I
10.1016/S0143-4160(03)00155-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Using confocal microscopy, we have examined the increases in [Ca2+](i) evoked by sodium channel toxins in cells labelled with the fluorescent dye INDO-1. We describe a new image analysis method that improves the detection of region-specific, toxin-induced patterns of change of intracellular calcium. This method is based on correction of global image motion followed by calculation of the strength of correlation between calcium changes in "seed" or reference pixels chosen to represent different regions of cells and those in other regions of the image. When the selected "seed" pixel was chosen to be in either varicosities or neurites, correlations were detected in the same regions of other cells as well as in the soma, indicating specific but spatially distinct patterns of behaviour. Control images (without changes in [Ca2+](i)) did not reveal significant interpixel correlations. The ability to recognize correlated patterns of calcium change in different regions of cells was greatly improved by correction for global motion. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 85
页数:7
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