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Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines

Doppel, a prion-like protein, is a GPI-membrane anchored protein generally not expressed in the Central Nervous System (CNS) of different mammalian species, including human. Nevertheless, in astrocytomas, a particular kind of glial tumors, the doppel encoding gene (PRND) is over-expressed and the co...

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Autores principales: Sbalchiero, Elena, Azzalin, Alberto, Palumbo, Silvia, Barbieri, Giulia, Arias, Agustina, Simonelli, Luca, Ferretti, Luca, Comincini, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618817/
https://www.ncbi.nlm.nih.gov/pubmed/18607068
http://dx.doi.org/10.3233/CLO-2008-0429
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author Sbalchiero, Elena
Azzalin, Alberto
Palumbo, Silvia
Barbieri, Giulia
Arias, Agustina
Simonelli, Luca
Ferretti, Luca
Comincini, Sergio
author_facet Sbalchiero, Elena
Azzalin, Alberto
Palumbo, Silvia
Barbieri, Giulia
Arias, Agustina
Simonelli, Luca
Ferretti, Luca
Comincini, Sergio
author_sort Sbalchiero, Elena
collection PubMed
description Doppel, a prion-like protein, is a GPI-membrane anchored protein generally not expressed in the Central Nervous System (CNS) of different mammalian species, including human. Nevertheless, in astrocytomas, a particular kind of glial tumors, the doppel encoding gene (PRND) is over-expressed and the corresponding protein product (Dpl) is ectopically localized in the cytoplasm of the tumor cells. In this study we have analysed the sub-cellular localization of Dpl using double-immunofluorescence staining and confocal microscopy examinations in two astrocytoma-derived human cell lines (IPDDC-A2 and D384-MG). Our results confirmed that Dpl is localized in the cytoplasm of the astrocytoma cells and indicated that it is mostly associated with Lamp-1 and Limp-2 positive lysosomal vesicles and, marginally, to the Golgi apparatus and other cellular organelles. Noticeably, none of the examined tumor cells showed a membrane-Dpl localization. The membrane-associated Dpl expression was restored after the transfection of the astrocytoma cells with mutated Dpl-expression vectors in its glycosylation sites. Additionally, Dpl showed altered expression and traffic using the acidotropic agent ammonium chloride, leading to the accumulation of Dpl in nascent exocytic vesicles. Altogether, these results indicated that in the astrocytic tumor cells Dpl has an altered biosynthetic trafficking, likely derived from abnormal post-translational processes: these modifications do not permit the localization of Dpl in correspondence of the plasma membrane and lead to its intracellular accumulation in the lysosomes. In these proteolytic compartments, the astrocytic tumor cells might provide to the degradation of the excess of a potentially cytotoxic Dpl product.
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spelling pubmed-46188172016-01-12 Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines Sbalchiero, Elena Azzalin, Alberto Palumbo, Silvia Barbieri, Giulia Arias, Agustina Simonelli, Luca Ferretti, Luca Comincini, Sergio Cell Oncol Other Doppel, a prion-like protein, is a GPI-membrane anchored protein generally not expressed in the Central Nervous System (CNS) of different mammalian species, including human. Nevertheless, in astrocytomas, a particular kind of glial tumors, the doppel encoding gene (PRND) is over-expressed and the corresponding protein product (Dpl) is ectopically localized in the cytoplasm of the tumor cells. In this study we have analysed the sub-cellular localization of Dpl using double-immunofluorescence staining and confocal microscopy examinations in two astrocytoma-derived human cell lines (IPDDC-A2 and D384-MG). Our results confirmed that Dpl is localized in the cytoplasm of the astrocytoma cells and indicated that it is mostly associated with Lamp-1 and Limp-2 positive lysosomal vesicles and, marginally, to the Golgi apparatus and other cellular organelles. Noticeably, none of the examined tumor cells showed a membrane-Dpl localization. The membrane-associated Dpl expression was restored after the transfection of the astrocytoma cells with mutated Dpl-expression vectors in its glycosylation sites. Additionally, Dpl showed altered expression and traffic using the acidotropic agent ammonium chloride, leading to the accumulation of Dpl in nascent exocytic vesicles. Altogether, these results indicated that in the astrocytic tumor cells Dpl has an altered biosynthetic trafficking, likely derived from abnormal post-translational processes: these modifications do not permit the localization of Dpl in correspondence of the plasma membrane and lead to its intracellular accumulation in the lysosomes. In these proteolytic compartments, the astrocytic tumor cells might provide to the degradation of the excess of a potentially cytotoxic Dpl product. IOS Press 2008 2008-07-01 /pmc/articles/PMC4618817/ /pubmed/18607068 http://dx.doi.org/10.3233/CLO-2008-0429 Text en Copyright © 2008 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Sbalchiero, Elena
Azzalin, Alberto
Palumbo, Silvia
Barbieri, Giulia
Arias, Agustina
Simonelli, Luca
Ferretti, Luca
Comincini, Sergio
Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title_full Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title_fullStr Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title_full_unstemmed Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title_short Altered Cellular Distribution and Sub-Cellular Sorting of Doppel (Dpl) Protein in Human Astrocytoma Cell Lines
title_sort altered cellular distribution and sub-cellular sorting of doppel (dpl) protein in human astrocytoma cell lines
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618817/
https://www.ncbi.nlm.nih.gov/pubmed/18607068
http://dx.doi.org/10.3233/CLO-2008-0429
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