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Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein

BACKGROUND: Cancer cell-derived extracellular vesicles (EVs) have previously been shown to contribute to pre-metastatic niche formation. Specifically, aggressive tumors secrete pro-metastatic EVs that travel in the circulation to distant organs to modulate the microenvironment for future metastatic...

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Autores principales: Busatto, Sara, Yang, Yubo, Walker, Sierra A., Davidovich, Irina, Lin, Wan-Hsin, Lewis-Tuffin, Laura, Anastasiadis, Panagiotis Z., Sarkaria, Jann, Talmon, Yeshayahu, Wurtz, Gregory, Wolfram, Joy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648399/
https://www.ncbi.nlm.nih.gov/pubmed/33160390
http://dx.doi.org/10.1186/s12951-020-00722-2
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author Busatto, Sara
Yang, Yubo
Walker, Sierra A.
Davidovich, Irina
Lin, Wan-Hsin
Lewis-Tuffin, Laura
Anastasiadis, Panagiotis Z.
Sarkaria, Jann
Talmon, Yeshayahu
Wurtz, Gregory
Wolfram, Joy
author_facet Busatto, Sara
Yang, Yubo
Walker, Sierra A.
Davidovich, Irina
Lin, Wan-Hsin
Lewis-Tuffin, Laura
Anastasiadis, Panagiotis Z.
Sarkaria, Jann
Talmon, Yeshayahu
Wurtz, Gregory
Wolfram, Joy
author_sort Busatto, Sara
collection PubMed
description BACKGROUND: Cancer cell-derived extracellular vesicles (EVs) have previously been shown to contribute to pre-metastatic niche formation. Specifically, aggressive tumors secrete pro-metastatic EVs that travel in the circulation to distant organs to modulate the microenvironment for future metastatic spread. Previous studies have focused on the interface between pro-metastatic EVs and epithelial/endothelial cells in the pre-metastatic niche. However, EV interactions with circulating components such as low-density lipoprotein (LDL) have been overlooked. RESULTS: This study demonstrates that EVs derived from brain metastases cells (Br-EVs) and corresponding regular cancer cells (Reg-EVs) display different interactions with LDL. Specifically, Br-EVs trigger LDL aggregation, and the presence of LDL accelerates Br-EV uptake by monocytes, which are key components in the brain metastatic niche. CONCLUSIONS: Collectively, these data are the first to demonstrate that pro-metastatic EVs display distinct interactions with LDL, which impacts monocyte internalization of EVs. [Image: see text]
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spelling pubmed-76483992020-11-09 Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein Busatto, Sara Yang, Yubo Walker, Sierra A. Davidovich, Irina Lin, Wan-Hsin Lewis-Tuffin, Laura Anastasiadis, Panagiotis Z. Sarkaria, Jann Talmon, Yeshayahu Wurtz, Gregory Wolfram, Joy J Nanobiotechnology Research BACKGROUND: Cancer cell-derived extracellular vesicles (EVs) have previously been shown to contribute to pre-metastatic niche formation. Specifically, aggressive tumors secrete pro-metastatic EVs that travel in the circulation to distant organs to modulate the microenvironment for future metastatic spread. Previous studies have focused on the interface between pro-metastatic EVs and epithelial/endothelial cells in the pre-metastatic niche. However, EV interactions with circulating components such as low-density lipoprotein (LDL) have been overlooked. RESULTS: This study demonstrates that EVs derived from brain metastases cells (Br-EVs) and corresponding regular cancer cells (Reg-EVs) display different interactions with LDL. Specifically, Br-EVs trigger LDL aggregation, and the presence of LDL accelerates Br-EV uptake by monocytes, which are key components in the brain metastatic niche. CONCLUSIONS: Collectively, these data are the first to demonstrate that pro-metastatic EVs display distinct interactions with LDL, which impacts monocyte internalization of EVs. [Image: see text] BioMed Central 2020-11-07 /pmc/articles/PMC7648399/ /pubmed/33160390 http://dx.doi.org/10.1186/s12951-020-00722-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Busatto, Sara
Yang, Yubo
Walker, Sierra A.
Davidovich, Irina
Lin, Wan-Hsin
Lewis-Tuffin, Laura
Anastasiadis, Panagiotis Z.
Sarkaria, Jann
Talmon, Yeshayahu
Wurtz, Gregory
Wolfram, Joy
Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title_full Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title_fullStr Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title_full_unstemmed Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title_short Brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
title_sort brain metastases-derived extracellular vesicles induce binding and aggregation of low-density lipoprotein
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648399/
https://www.ncbi.nlm.nih.gov/pubmed/33160390
http://dx.doi.org/10.1186/s12951-020-00722-2
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