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Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform

Extracellular vesicles (EVs) are cell-derived membranous structures carrying transmembrane proteins and luminal cargo. Their complex cargo requires pH stability in EVs while traversing diverse body fluids. We used a filtration-based platform to capture and stabilize EVs based on their size and studi...

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Autores principales: Riazanski, Vladimir, Mauleon, Gerardo, Lucas, Kilean, Walker, Samuel, Zimnicka, Adriana M., McGrath, James L., Nelson, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748679/
https://www.ncbi.nlm.nih.gov/pubmed/35013561
http://dx.doi.org/10.1038/s42003-021-02965-7
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author Riazanski, Vladimir
Mauleon, Gerardo
Lucas, Kilean
Walker, Samuel
Zimnicka, Adriana M.
McGrath, James L.
Nelson, Deborah J.
author_facet Riazanski, Vladimir
Mauleon, Gerardo
Lucas, Kilean
Walker, Samuel
Zimnicka, Adriana M.
McGrath, James L.
Nelson, Deborah J.
author_sort Riazanski, Vladimir
collection PubMed
description Extracellular vesicles (EVs) are cell-derived membranous structures carrying transmembrane proteins and luminal cargo. Their complex cargo requires pH stability in EVs while traversing diverse body fluids. We used a filtration-based platform to capture and stabilize EVs based on their size and studied their pH regulation at the single EV level. Dead-end filtration facilitated EV capture in the pores of an ultrathin (100 nm thick) and nanoporous silicon nitride (NPN) membrane within a custom microfluidic device. Immobilized EVs were rapidly exposed to test solution changes driven across the backside of the membrane using tangential flow without exposing the EVs to fluid shear forces. The epithelial sodium-hydrogen exchanger, NHE1, is a ubiquitous plasma membrane protein tasked with the maintenance of cytoplasmic pH at neutrality. We show that NHE1 identified on the membrane of EVs is functional in the maintenance of pH neutrality within single vesicles. This is the first mechanistic description of EV function on the single vesicle level.
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spelling pubmed-87486792022-01-20 Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform Riazanski, Vladimir Mauleon, Gerardo Lucas, Kilean Walker, Samuel Zimnicka, Adriana M. McGrath, James L. Nelson, Deborah J. Commun Biol Article Extracellular vesicles (EVs) are cell-derived membranous structures carrying transmembrane proteins and luminal cargo. Their complex cargo requires pH stability in EVs while traversing diverse body fluids. We used a filtration-based platform to capture and stabilize EVs based on their size and studied their pH regulation at the single EV level. Dead-end filtration facilitated EV capture in the pores of an ultrathin (100 nm thick) and nanoporous silicon nitride (NPN) membrane within a custom microfluidic device. Immobilized EVs were rapidly exposed to test solution changes driven across the backside of the membrane using tangential flow without exposing the EVs to fluid shear forces. The epithelial sodium-hydrogen exchanger, NHE1, is a ubiquitous plasma membrane protein tasked with the maintenance of cytoplasmic pH at neutrality. We show that NHE1 identified on the membrane of EVs is functional in the maintenance of pH neutrality within single vesicles. This is the first mechanistic description of EV function on the single vesicle level. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748679/ /pubmed/35013561 http://dx.doi.org/10.1038/s42003-021-02965-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Riazanski, Vladimir
Mauleon, Gerardo
Lucas, Kilean
Walker, Samuel
Zimnicka, Adriana M.
McGrath, James L.
Nelson, Deborah J.
Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title_full Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title_fullStr Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title_full_unstemmed Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title_short Real time imaging of single extracellular vesicle pH regulation in a microfluidic cross-flow filtration platform
title_sort real time imaging of single extracellular vesicle ph regulation in a microfluidic cross-flow filtration platform
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748679/
https://www.ncbi.nlm.nih.gov/pubmed/35013561
http://dx.doi.org/10.1038/s42003-021-02965-7
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