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Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids
The prevalence of end-stage kidney disease (ESKD) is rapidly increasing with the need for regenerative therapies. Adult stem cell derived kidney tubuloids have the potential to functionally mimic the adult kidney tubule, but still lack the expression of important transport proteins needed for waste...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284832/ https://www.ncbi.nlm.nih.gov/pubmed/35841001 http://dx.doi.org/10.1186/s12951-022-01506-6 |
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author | Lindoso, Rafael Soares Yousef Yengej, Fjodor A. Voellmy, Franziska Altelaar, Maarten Mancheño Juncosa, Estela Tsikari, Theano Ammerlaan, Carola M. E. Van Balkom, Bas W. M. Rookmaaker, Maarten B. Verhaar, Marianne C. Masereeuw, Rosalinde |
author_facet | Lindoso, Rafael Soares Yousef Yengej, Fjodor A. Voellmy, Franziska Altelaar, Maarten Mancheño Juncosa, Estela Tsikari, Theano Ammerlaan, Carola M. E. Van Balkom, Bas W. M. Rookmaaker, Maarten B. Verhaar, Marianne C. Masereeuw, Rosalinde |
author_sort | Lindoso, Rafael Soares |
collection | PubMed |
description | The prevalence of end-stage kidney disease (ESKD) is rapidly increasing with the need for regenerative therapies. Adult stem cell derived kidney tubuloids have the potential to functionally mimic the adult kidney tubule, but still lack the expression of important transport proteins needed for waste removal. Here, we investigated the potential of extracellular vesicles (EVs) obtained from matured kidney tubular epithelial cells to modulate in vitro tubuloids functional maturation. We focused on organic anion transporter 1 (OAT1), one of the most important proteins involved in endogenous waste excretion. First, we show that EVs from engineered proximal tubule cells increased the expression of several transcription factors and epithelial transporters, resulting in improved OAT1 transport capacity. Next, a more in-depth proteomic data analysis showed that EVs can trigger various biological pathways, including mesenchymal-to-epithelial transition, which is crucial in the tubular epithelial maturation. Moreover, we demonstrated that the combination of EVs and tubuloid-derived cells can be used as part of a bioartificial kidney to generate a tight polarized epithelial monolayer with formation of dense cilia structures. In conclusion, EVs from kidney tubular epithelial cells can phenotypically improve in vitro tubuloid maturation, thereby enhancing their potential as functional units in regenerative or renal replacement therapies. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01506-6. |
format | Online Article Text |
id | pubmed-9284832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92848322022-07-16 Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids Lindoso, Rafael Soares Yousef Yengej, Fjodor A. Voellmy, Franziska Altelaar, Maarten Mancheño Juncosa, Estela Tsikari, Theano Ammerlaan, Carola M. E. Van Balkom, Bas W. M. Rookmaaker, Maarten B. Verhaar, Marianne C. Masereeuw, Rosalinde J Nanobiotechnology Research The prevalence of end-stage kidney disease (ESKD) is rapidly increasing with the need for regenerative therapies. Adult stem cell derived kidney tubuloids have the potential to functionally mimic the adult kidney tubule, but still lack the expression of important transport proteins needed for waste removal. Here, we investigated the potential of extracellular vesicles (EVs) obtained from matured kidney tubular epithelial cells to modulate in vitro tubuloids functional maturation. We focused on organic anion transporter 1 (OAT1), one of the most important proteins involved in endogenous waste excretion. First, we show that EVs from engineered proximal tubule cells increased the expression of several transcription factors and epithelial transporters, resulting in improved OAT1 transport capacity. Next, a more in-depth proteomic data analysis showed that EVs can trigger various biological pathways, including mesenchymal-to-epithelial transition, which is crucial in the tubular epithelial maturation. Moreover, we demonstrated that the combination of EVs and tubuloid-derived cells can be used as part of a bioartificial kidney to generate a tight polarized epithelial monolayer with formation of dense cilia structures. In conclusion, EVs from kidney tubular epithelial cells can phenotypically improve in vitro tubuloid maturation, thereby enhancing their potential as functional units in regenerative or renal replacement therapies. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01506-6. BioMed Central 2022-07-15 /pmc/articles/PMC9284832/ /pubmed/35841001 http://dx.doi.org/10.1186/s12951-022-01506-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Lindoso, Rafael Soares Yousef Yengej, Fjodor A. Voellmy, Franziska Altelaar, Maarten Mancheño Juncosa, Estela Tsikari, Theano Ammerlaan, Carola M. E. Van Balkom, Bas W. M. Rookmaaker, Maarten B. Verhaar, Marianne C. Masereeuw, Rosalinde Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title | Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title_full | Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title_fullStr | Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title_full_unstemmed | Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title_short | Differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
title_sort | differentiated kidney tubular cell-derived extracellular vesicles enhance maturation of tubuloids |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9284832/ https://www.ncbi.nlm.nih.gov/pubmed/35841001 http://dx.doi.org/10.1186/s12951-022-01506-6 |
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