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Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells

Fractal morphometry was used to investigate the ultrastructural features of the plasma membrane, perinuclear membrane and nuclear chromatin in SK‐BR‐3 human breast cancer cells undergoing apoptosis. Cells were incubated with 1 μM calcimycin (A23187) for 24 h. Cells in the early stage of apoptosis ha...

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Detalles Bibliográficos
Autores principales: Castelli, Christian, Losa, Gabriele A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617388/
https://www.ncbi.nlm.nih.gov/pubmed/11790854
http://dx.doi.org/10.1155/2001/828309
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author Castelli, Christian
Losa, Gabriele A.
author_facet Castelli, Christian
Losa, Gabriele A.
author_sort Castelli, Christian
collection PubMed
description Fractal morphometry was used to investigate the ultrastructural features of the plasma membrane, perinuclear membrane and nuclear chromatin in SK‐BR‐3 human breast cancer cells undergoing apoptosis. Cells were incubated with 1 μM calcimycin (A23187) for 24 h. Cells in the early stage of apoptosis had fractal dimension (FD) values indicating that their plasma membranes were less rough (lower FD) than those of control cells, while their perinuclear membranes were unaffected. Changes of the chromatin texture within the entire nucleus and in selected nuclear domains were more pronounced in treated cells. This confirms that the morphological reorganization imputable to a loss of structural complexity (reduced FD) occurs in the early stage of apoptosis, is accompanied by the inhibition of distinct enzymatic events and precedes the onset of conventional cellular markers, which can only be detected during the active phases of the apoptotic process.
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spelling pubmed-46173882016-01-12 Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells Castelli, Christian Losa, Gabriele A. Anal Cell Pathol Other Fractal morphometry was used to investigate the ultrastructural features of the plasma membrane, perinuclear membrane and nuclear chromatin in SK‐BR‐3 human breast cancer cells undergoing apoptosis. Cells were incubated with 1 μM calcimycin (A23187) for 24 h. Cells in the early stage of apoptosis had fractal dimension (FD) values indicating that their plasma membranes were less rough (lower FD) than those of control cells, while their perinuclear membranes were unaffected. Changes of the chromatin texture within the entire nucleus and in selected nuclear domains were more pronounced in treated cells. This confirms that the morphological reorganization imputable to a loss of structural complexity (reduced FD) occurs in the early stage of apoptosis, is accompanied by the inhibition of distinct enzymatic events and precedes the onset of conventional cellular markers, which can only be detected during the active phases of the apoptotic process. IOS Press 2001 2001-01-01 /pmc/articles/PMC4617388/ /pubmed/11790854 http://dx.doi.org/10.1155/2001/828309 Text en Copyright © 2001 Hindawi Publishing Corporation.
spellingShingle Other
Castelli, Christian
Losa, Gabriele A.
Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title_full Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title_fullStr Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title_full_unstemmed Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title_short Ultrastructural Complexity of Nuclear Components During Early Apoptotic Phases in Breast Cancer Cells
title_sort ultrastructural complexity of nuclear components during early apoptotic phases in breast cancer cells
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617388/
https://www.ncbi.nlm.nih.gov/pubmed/11790854
http://dx.doi.org/10.1155/2001/828309
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