Spatial distribution patterns of interphase centromeres during retinoic acid-induced differentiation of promyelocytic leukemia cells

被引:33
作者
Beil, M [1 ]
Dürschmied, D
Paschke, S
Schreiner, B
Nolte, U
Bruel, A
Irinopoulou, T
机构
[1] Univ Ulm, Dept Internal Med 1, D-89070 Ulm, Germany
[2] Imagenium, Paris, France
[3] Univ Ulm, Dept Human Genet, D-89070 Ulm, Germany
[4] Univ Paris 07, Hosp St Louis, Inst Hematol, Paris, France
[5] Hop Broussais, INSERM Unit 430, F-75674 Paris, France
来源
CYTOMETRY | 2002年 / 47卷 / 04期
关键词
confocal microscopy; centromere; differentiation; heterochromatin; minimal spanning tree; promyelocytic leukemia; 3D image analysis;
D O I
10.1002/cyto.10077
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The pericentromeric heterochromatin is an important element for the regulation of gene silencing. Its spatial distribution during interphase appears to be celltype specific. This study analyzes three-dimensional (3D) centromere distribution patterns during cellular differentiation along the neutrophil pathway. Methods: Differentiation of the promyelocytic leukemia cell line NB4 was induced by retinoic acid, Centromeres in interphase nuclei were visualized by immunofluorescence staining of centromere-associated proteins with CREST serum. 3D images of nuclei were obtained by confocal microscopy. Automated methods for the segmentation of point-like objects in 3D images were implemented to detect the position of centromeres. Features of centromere localization patterns were determined by constructing the minimal spanning tree of the centromere distribution. Results: In differentiated NB4 cells, the number of centromere conglomerates (chromocenters) was decreased and the distance between chromocenters was increased as compared with untreated controls. The nuclear volume did not differ between the two groups. Conclusions: The measured rearrangement of centromeres indicates a progressive clustering of heterochromatin and a global remodeling of interphase chromosome territories during differentiation of NB4 cells. The developed methods for the analysis of 3D centromere distribution patterns provide the opportunity for a fast and objective analysis of heterochromatin remodeling. (C) 2002 Wiley-Liss, Inc.
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页码:217 / 225
页数:9
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