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磷酸化Ki-67的三维结构:一项使用氟纳米金的荧光和电子断层扫描对比研究

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

作者信息

Cheutin Thierry, O'Donohue Marie-Françoise, Beorchia Adrien, Klein Christophe, Kaplan Hervé, Ploton Dominique

机构信息

Unité MéDian, CNRS UMR 6142, UFR de Pharmacie, 51 rue Cognacq-Jay, 51096 Reims Cedex, France.

出版信息

J Histochem Cytochem. 2003 Nov;51(11):1411-23. doi: 10.1177/002215540305101102.

Abstract

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.

摘要

单克隆抗体(MAb)Ki-67常用于临床研究以评估肿瘤的生长分数。然而,尽管一些生化数据强烈表明它可能参与染色质的组织,但Ki-67单克隆抗体所检测到的蛋白pKi-67的作用仍不清楚。为了更好地理解pKi-67的功能组织,我们通过共聚焦显微镜和电子断层扫描研究了其在间期细胞中的三维分布。FluoroNanogold是一种将致密标记物与荧光染料结合的单一探针,用于在光学和超微结构水平上研究pKi-67的组织情况。共聚焦显微镜观察后进行三维重建显示,pKi-67在核仁周围形成一个壳层。双重标记实验表明,pKi-67与核仁周围异染色质共定位。电子显微镜研究证实了这种紧密关联,并表明pKi-67既不在核仁的纤维成分中,也不在颗粒成分中。最后,电子断层扫描的空间分析表明,pKi-67形成直径为250 - 300 nm的索状结构,这些索状结构本身由30 - 50 nm厚的纤维组成。这些详细的原位比较分析强烈表明pKi-67参与了核仁周围染色质的高级组织形成。

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