Cargando…

Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth

The contributions of mesenchymal stem cells (MSCs) to tumour growth and stroma formation are poorly understood. Tumour cells can transfer genetic information and modulate cell signalling in other cells through the release of extracellular vesicles (EVs). We examined the contribution of EV-mediated i...

Descripción completa

Detalles Bibliográficos
Autores principales: Haga, Hiroaki, Yan, Irene K., Takahashi, Kenji, Wood, Joseph, Zubair, Abba, Patel, Tushar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283029/
https://www.ncbi.nlm.nih.gov/pubmed/25557794
http://dx.doi.org/10.3402/jev.v4.24900
_version_ 1782351207463911424
author Haga, Hiroaki
Yan, Irene K.
Takahashi, Kenji
Wood, Joseph
Zubair, Abba
Patel, Tushar
author_facet Haga, Hiroaki
Yan, Irene K.
Takahashi, Kenji
Wood, Joseph
Zubair, Abba
Patel, Tushar
author_sort Haga, Hiroaki
collection PubMed
description The contributions of mesenchymal stem cells (MSCs) to tumour growth and stroma formation are poorly understood. Tumour cells can transfer genetic information and modulate cell signalling in other cells through the release of extracellular vesicles (EVs). We examined the contribution of EV-mediated inter-cellular signalling between bone marrow MSCs and tumour cells in human cholangiocarcinoma, highly desmoplastic cancers that are characterized by tumour cells closely intertwined within a dense fibrous stroma. Exposure of MSCs to tumour cell–derived EVs enhanced MSC migratory capability and expression of alpha-smooth muscle actin mRNA, in addition to mRNA expression and release of CXCL-1, CCL2 and IL-6. Conditioned media from MSCs exposed to tumour cell–derived EVs increased STAT-3 phosphorylation and proliferation in tumour cells. These effects were completely blocked by anti-IL-6R antibody. In conclusion, tumour cell–derived EVs can contribute to the generation of tumour stroma through fibroblastic differentiation of MSCs, and can also selectively modulate the cellular release of soluble factors such as IL-6 by MSCs that can, in turn, alter tumour cell proliferation. Thus, malignant cells can “educate” MSCs to induce local microenvironmental changes that enhance tumour cell growth.
format Online
Article
Text
id pubmed-4283029
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Co-Action Publishing
record_format MEDLINE/PubMed
spelling pubmed-42830292015-01-26 Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth Haga, Hiroaki Yan, Irene K. Takahashi, Kenji Wood, Joseph Zubair, Abba Patel, Tushar J Extracell Vesicles Original Research Article The contributions of mesenchymal stem cells (MSCs) to tumour growth and stroma formation are poorly understood. Tumour cells can transfer genetic information and modulate cell signalling in other cells through the release of extracellular vesicles (EVs). We examined the contribution of EV-mediated inter-cellular signalling between bone marrow MSCs and tumour cells in human cholangiocarcinoma, highly desmoplastic cancers that are characterized by tumour cells closely intertwined within a dense fibrous stroma. Exposure of MSCs to tumour cell–derived EVs enhanced MSC migratory capability and expression of alpha-smooth muscle actin mRNA, in addition to mRNA expression and release of CXCL-1, CCL2 and IL-6. Conditioned media from MSCs exposed to tumour cell–derived EVs increased STAT-3 phosphorylation and proliferation in tumour cells. These effects were completely blocked by anti-IL-6R antibody. In conclusion, tumour cell–derived EVs can contribute to the generation of tumour stroma through fibroblastic differentiation of MSCs, and can also selectively modulate the cellular release of soluble factors such as IL-6 by MSCs that can, in turn, alter tumour cell proliferation. Thus, malignant cells can “educate” MSCs to induce local microenvironmental changes that enhance tumour cell growth. Co-Action Publishing 2015-01-02 /pmc/articles/PMC4283029/ /pubmed/25557794 http://dx.doi.org/10.3402/jev.v4.24900 Text en © 2015 Hiroaki Haga et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Haga, Hiroaki
Yan, Irene K.
Takahashi, Kenji
Wood, Joseph
Zubair, Abba
Patel, Tushar
Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title_full Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title_fullStr Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title_full_unstemmed Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title_short Tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
title_sort tumour cell–derived extracellular vesicles interact with mesenchymal stem cells to modulate the microenvironment and enhance cholangiocarcinoma growth
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283029/
https://www.ncbi.nlm.nih.gov/pubmed/25557794
http://dx.doi.org/10.3402/jev.v4.24900
work_keys_str_mv AT hagahiroaki tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth
AT yanirenek tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth
AT takahashikenji tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth
AT woodjoseph tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth
AT zubairabba tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth
AT pateltushar tumourcellderivedextracellularvesiclesinteractwithmesenchymalstemcellstomodulatethemicroenvironmentandenhancecholangiocarcinomagrowth