Development of a multistage classifier for a monitoring system of cell activity based on imaging of chromosomal dynamics

被引:17
作者
Gambe, Arni E.
Ono, Rika Maniwa
Matsunaga, Sachihiro
Kutsuna, Natsumaro
Higaki, Takumi
Higashi, Tsunehito
Hasezawa, Seiichiro
Uchiyama, Susumu
Fukui, Kiichi
机构
[1] Osaka Univ, Grad Sch Engn, Dept Biotechnol, Suita, Osaka 5650871, Japan
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Chiba 2778562, Japan
关键词
multistage linear discriminant classifier; cell-cycle phases; classification;
D O I
10.1002/cyto.a.20378
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Cell-based assays utilizing digital image cytometry yield multivariate sets of information measuring the efficacy of medicines/chemicals. The use of a HeLa cell line that expresses a GFP-Histone-H1 fusion protein further enhances the performance of these systems, avoiding the use of dyes that may have detrimental influence on cells. Aside from the mitotic index, the distribution of the cell-cycle phases during mitosis can be used as measures of drug/treatment efficacy. Quantification of these parameters, however, requires skill and is time consuming. The purpose of this research was therefore to create a classifier to be incorporated into a system that can automaiically identify the cell-cycle phases in a given image. Methods: Features based on the shape and texture of the chromosomal regions in images of live Hela cells were measured and analyzed. linear discriminant functions were calculated for the eight cell-cycle phases: interphase, prophase, prometaphase, metaphase, early anaphase, anaphase, telophase and cytokinesis. Results: The multistage linear discriminant classifier developed had an average classification efficiency of 87-30%. Conclusion: We demonstrated the possibility of creating a classifier to discriminate between cell-cycle phases using shape and texture features of chromosomal regions. The classifier can be fused to an algorithm for image segmentation, forming a system to automatically and rapidly measure the aforementioned parameters. The results can then be collated to constitute an assay assessing the effects of a drug or treatment on mammalian cells. (c) 2007 International Society for Analytical Cytology.
引用
收藏
页码:286 / 296
页数:11
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