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The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities

BACKGROUND: In a previous work we showed for the first time that human tumor cells secrete Hsp60 via exosomes, which are considered immunologically active microvesicles involved in tumor progression. This finding raised questions concerning the route followed by Hsp60 to reach the exosomes, its loca...

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Autores principales: Campanella, Claudia, Bucchieri, Fabio, Merendino, Anna M., Fucarino, Alberto, Burgio, Giosalba, Corona, Davide F. V., Barbieri, Giovanna, David, Sabrina, Farina, Felicia, Zummo, Giovanni, de Macario, Everly Conway, Macario, Alberto J. L., Cappello, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405006/
https://www.ncbi.nlm.nih.gov/pubmed/22848686
http://dx.doi.org/10.1371/journal.pone.0042008
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author Campanella, Claudia
Bucchieri, Fabio
Merendino, Anna M.
Fucarino, Alberto
Burgio, Giosalba
Corona, Davide F. V.
Barbieri, Giovanna
David, Sabrina
Farina, Felicia
Zummo, Giovanni
de Macario, Everly Conway
Macario, Alberto J. L.
Cappello, Francesco
author_facet Campanella, Claudia
Bucchieri, Fabio
Merendino, Anna M.
Fucarino, Alberto
Burgio, Giosalba
Corona, Davide F. V.
Barbieri, Giovanna
David, Sabrina
Farina, Felicia
Zummo, Giovanni
de Macario, Everly Conway
Macario, Alberto J. L.
Cappello, Francesco
author_sort Campanella, Claudia
collection PubMed
description BACKGROUND: In a previous work we showed for the first time that human tumor cells secrete Hsp60 via exosomes, which are considered immunologically active microvesicles involved in tumor progression. This finding raised questions concerning the route followed by Hsp60 to reach the exosomes, its location in them, and whether Hsp60 can be secreted also via other mechanisms, e.g., by the Golgi. We addressed these issues in the work presented here. PRINCIPAL FINDINGS: We found that Hsp60 localizes in the tumor cell plasma membrane, is associated with lipid rafts, and ends up in the exosomal membrane. We also found evidence that Hsp60 localizes in the Golgi apparatus and its secretion is prevented by an inhibitor of this organelle. CONCLUSIONS/SIGNIFICANCE: We propose a multistage process for the translocation of Hsp60 from the inside to the outside of the cell that includes a combination of protein traffic pathways and, ultimately, presence of the chaperonin in the circulating blood. The new information presented should help in designing future strategies for research and for developing diagnostic-monitoring means useful in clinical oncology.
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spelling pubmed-34050062012-07-30 The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities Campanella, Claudia Bucchieri, Fabio Merendino, Anna M. Fucarino, Alberto Burgio, Giosalba Corona, Davide F. V. Barbieri, Giovanna David, Sabrina Farina, Felicia Zummo, Giovanni de Macario, Everly Conway Macario, Alberto J. L. Cappello, Francesco PLoS One Research Article BACKGROUND: In a previous work we showed for the first time that human tumor cells secrete Hsp60 via exosomes, which are considered immunologically active microvesicles involved in tumor progression. This finding raised questions concerning the route followed by Hsp60 to reach the exosomes, its location in them, and whether Hsp60 can be secreted also via other mechanisms, e.g., by the Golgi. We addressed these issues in the work presented here. PRINCIPAL FINDINGS: We found that Hsp60 localizes in the tumor cell plasma membrane, is associated with lipid rafts, and ends up in the exosomal membrane. We also found evidence that Hsp60 localizes in the Golgi apparatus and its secretion is prevented by an inhibitor of this organelle. CONCLUSIONS/SIGNIFICANCE: We propose a multistage process for the translocation of Hsp60 from the inside to the outside of the cell that includes a combination of protein traffic pathways and, ultimately, presence of the chaperonin in the circulating blood. The new information presented should help in designing future strategies for research and for developing diagnostic-monitoring means useful in clinical oncology. Public Library of Science 2012-07-25 /pmc/articles/PMC3405006/ /pubmed/22848686 http://dx.doi.org/10.1371/journal.pone.0042008 Text en Campanella et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Campanella, Claudia
Bucchieri, Fabio
Merendino, Anna M.
Fucarino, Alberto
Burgio, Giosalba
Corona, Davide F. V.
Barbieri, Giovanna
David, Sabrina
Farina, Felicia
Zummo, Giovanni
de Macario, Everly Conway
Macario, Alberto J. L.
Cappello, Francesco
The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title_full The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title_fullStr The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title_full_unstemmed The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title_short The Odyssey of Hsp60 from Tumor Cells to Other Destinations Includes Plasma Membrane-Associated Stages and Golgi and Exosomal Protein-Trafficking Modalities
title_sort odyssey of hsp60 from tumor cells to other destinations includes plasma membrane-associated stages and golgi and exosomal protein-trafficking modalities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405006/
https://www.ncbi.nlm.nih.gov/pubmed/22848686
http://dx.doi.org/10.1371/journal.pone.0042008
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