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Matrix mechanics and water permeation regulate extracellular vesicle transport
Cells release extracellular vesicles (EVs) to communicate over long distances, requiring EVs to traverse the extracellular matrix (ECM). However, given that the size of EVs is usually larger than the mesh size of the ECM, it is not clear how they can travel through the dense ECM. Here we show that i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075670/ https://www.ncbi.nlm.nih.gov/pubmed/32066904 http://dx.doi.org/10.1038/s41565-020-0636-2 |
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author | Lenzini, Stephen Bargi, Raymond Chung, Gina Shin, Jae-Won |
author_facet | Lenzini, Stephen Bargi, Raymond Chung, Gina Shin, Jae-Won |
author_sort | Lenzini, Stephen |
collection | PubMed |
description | Cells release extracellular vesicles (EVs) to communicate over long distances, requiring EVs to traverse the extracellular matrix (ECM). However, given that the size of EVs is usually larger than the mesh size of the ECM, it is not clear how they can travel through the dense ECM. Here we show that in contrast to synthetic nanoparticles, EVs readily transport through nanoporous ECM. Using engineered hydrogels, we demonstrate that the mechanical properties of the matrix regulate anomalous EV transport under confinement. Matrix stress relaxation allows EVs to overcome confinement, and a higher crosslinking density facilitates fluctuating transport motion through the polymer mesh, leading to free diffusion and fast transport. Furthermore, water permeation through aquaporin-1 mediates EV deformability, which further supports EV transport in hydrogels and decellularized matrix. Our results provide evidence of the nature of EV transport within confined environments and demonstrate an unexpected dependence on matrix mechanics and water permeation. |
format | Online Article Text |
id | pubmed-7075670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70756702020-08-17 Matrix mechanics and water permeation regulate extracellular vesicle transport Lenzini, Stephen Bargi, Raymond Chung, Gina Shin, Jae-Won Nat Nanotechnol Article Cells release extracellular vesicles (EVs) to communicate over long distances, requiring EVs to traverse the extracellular matrix (ECM). However, given that the size of EVs is usually larger than the mesh size of the ECM, it is not clear how they can travel through the dense ECM. Here we show that in contrast to synthetic nanoparticles, EVs readily transport through nanoporous ECM. Using engineered hydrogels, we demonstrate that the mechanical properties of the matrix regulate anomalous EV transport under confinement. Matrix stress relaxation allows EVs to overcome confinement, and a higher crosslinking density facilitates fluctuating transport motion through the polymer mesh, leading to free diffusion and fast transport. Furthermore, water permeation through aquaporin-1 mediates EV deformability, which further supports EV transport in hydrogels and decellularized matrix. Our results provide evidence of the nature of EV transport within confined environments and demonstrate an unexpected dependence on matrix mechanics and water permeation. 2020-02-17 2020-03 /pmc/articles/PMC7075670/ /pubmed/32066904 http://dx.doi.org/10.1038/s41565-020-0636-2 Text en Reprints and permission information is available online at www.nature.com/reprints (http://www.nature.com/reprints) . Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lenzini, Stephen Bargi, Raymond Chung, Gina Shin, Jae-Won Matrix mechanics and water permeation regulate extracellular vesicle transport |
title | Matrix mechanics and water permeation regulate extracellular vesicle transport |
title_full | Matrix mechanics and water permeation regulate extracellular vesicle transport |
title_fullStr | Matrix mechanics and water permeation regulate extracellular vesicle transport |
title_full_unstemmed | Matrix mechanics and water permeation regulate extracellular vesicle transport |
title_short | Matrix mechanics and water permeation regulate extracellular vesicle transport |
title_sort | matrix mechanics and water permeation regulate extracellular vesicle transport |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075670/ https://www.ncbi.nlm.nih.gov/pubmed/32066904 http://dx.doi.org/10.1038/s41565-020-0636-2 |
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