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Three-dimensional Organization of pKi-67: A Comparative Fluorescence and Electron Tomography Study Using Fluoronanogold

Authors :
Thierry Cheutin
Hervé Kaplan
Marie-Françoise O'Donohue
Dominique Ploton
Christophe Klein
Adrien Beorchia
Institut de génétique humaine (IGH)
Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Laboratoire de biologie moléculaire eucaryote (LBME)
Centre National de la Recherche Scientifique (CNRS)-Centre de Biologie Intégrative (CBI)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)
UTAP
Faculté de Médecine de Reims
Source :
Journal of Histochemistry and Cytochemistry, Journal of Histochemistry and Cytochemistry, Histochemical Society, 2016, 51 (11), pp.1411-1423. ⟨10.1177/002215540305101102⟩
Publication Year :
2003
Publisher :
SAGE Publications, 2003.

Abstract

International audience; 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.

Details

Language :
English
ISSN :
00221554
Database :
OpenAIRE
Journal :
Journal of Histochemistry and Cytochemistry, Journal of Histochemistry and Cytochemistry, Histochemical Society, 2016, 51 (11), pp.1411-1423. ⟨10.1177/002215540305101102⟩
Accession number :
edsair.doi.dedup.....13651ab7f84194ebbe477c50bac83563
Full Text :
https://doi.org/10.1177/002215540305101102⟩