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Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis

Extracellular signal-regulated kinases (ERK) 1, 2 and 3 are involved in cell proliferation and differentiation, and apoptosis; although ERK1/2 have been widely studied, limited knowledge on ERK3 is available. The present work aimed at investigating ERK3 distribution during cell cycle and apoptosis i...

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Detalles Bibliográficos
Autores principales: Aredia, F., Malatesta, M., Veneroni, P., Bottone, M.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698618/
https://www.ncbi.nlm.nih.gov/pubmed/26708186
http://dx.doi.org/10.4081/ejh.2015.2571
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author Aredia, F.
Malatesta, M.
Veneroni, P.
Bottone, M.G.
author_facet Aredia, F.
Malatesta, M.
Veneroni, P.
Bottone, M.G.
author_sort Aredia, F.
collection PubMed
description Extracellular signal-regulated kinases (ERK) 1, 2 and 3 are involved in cell proliferation and differentiation, and apoptosis; although ERK1/2 have been widely studied, limited knowledge on ERK3 is available. The present work aimed at investigating ERK3 distribution during cell cycle and apoptosis in human tumor HeLa cells. The analysis performed by double immunofluorescence and immunoelectron microscopy revealed that during interphase ERK3 is mainly resident in the nucleoplasm in association with ribonuclear proteins involved in early pre-mRNA splicing, it undergoes cell cycle-dependent redistribution and, during apoptosis, it remains in the nucleus in the form of massive nuclear aggregates, then moves to the cytoplasm and is finally extruded.
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spelling pubmed-46986182016-01-15 Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis Aredia, F. Malatesta, M. Veneroni, P. Bottone, M.G. Eur J Histochem Brief Report Extracellular signal-regulated kinases (ERK) 1, 2 and 3 are involved in cell proliferation and differentiation, and apoptosis; although ERK1/2 have been widely studied, limited knowledge on ERK3 is available. The present work aimed at investigating ERK3 distribution during cell cycle and apoptosis in human tumor HeLa cells. The analysis performed by double immunofluorescence and immunoelectron microscopy revealed that during interphase ERK3 is mainly resident in the nucleoplasm in association with ribonuclear proteins involved in early pre-mRNA splicing, it undergoes cell cycle-dependent redistribution and, during apoptosis, it remains in the nucleus in the form of massive nuclear aggregates, then moves to the cytoplasm and is finally extruded. PAGEPress Publications, Pavia, Italy 2015-12-01 /pmc/articles/PMC4698618/ /pubmed/26708186 http://dx.doi.org/10.4081/ejh.2015.2571 Text en ©Copyright F. Aredia et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Aredia, F.
Malatesta, M.
Veneroni, P.
Bottone, M.G.
Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title_full Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title_fullStr Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title_full_unstemmed Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title_short Analysis of ERK3 Intracellular Localization: Dynamic Distribution During Mitosis and Apoptosis
title_sort analysis of erk3 intracellular localization: dynamic distribution during mitosis and apoptosis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698618/
https://www.ncbi.nlm.nih.gov/pubmed/26708186
http://dx.doi.org/10.4081/ejh.2015.2571
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