Three-dimensional organization of pKi-67: a comparative fluorescence and electron tomography study using fluoronanogold

被引:27
作者
Cheutin, T
O'Donohue, MF
Beorchia, A
Klein, C
Kaplan, H
Ploton, D
机构
[1] UFR Pharm, CNRS, UMR 6142, Unite MeDian, F-51096 Reims, France
[2] UFR Sci, DTI, UMR 6107, Reims, France
[3] Inst Biomed Cordeliers, INSERM, IFR58, Serv Commun Imagerie Cellulaire & Cytometrie, Paris, France
[4] IFR53, Reims, France
关键词
confocal microscopy; electron tomography; heterochromatin; Ki-67; antigen; nucleolus;
D O I
10.1177/002215540305101102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The monoclonal antibody (MAb) Ki-67 is routinely used in clinical studies to estimate the growth fraction of tumors. However, the role of pKi-67, the protein detected by the Ki-67 MAb, remains elusive, although some biochemical data strongly suggest that it might organize chromatin. To better understand the functional organization of pKi-67, we studied its three-dimensional distribution in interphase cells by confocal microscopy and electron tomography. FluoroNanogold, a single probe combining a dense marker with a fluorescent dye, was used to investigate pKi-67 organization at the optical and ultrastructural levels. Observation by confocal microscopy followed by 3D reconstruction showed that pKi-67 forms a shell around the nucleoli. Double labeling experiments revealed that pKi-67 co-localizes with perinucleolar heterochromatin. Electron microscopy studies confirmed this close association and demonstrated that pKi-67 is located neither in the fibrillar nor in the granular components of the nucleolus. Finally, spatial analyses by electron tomography showed that pKi-67 forms cords 250-300 nm in diameter, which are themselves composed of 30-50-nm-thick fibers. These detailed comparative in situ analyses strongly suggest the involvement of pKi-67 in the higher-order organization of perinucleolar chromatin.
引用
收藏
页码:1411 / 1423
页数:13
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