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Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions

Patients with end-stage kidney disease (ESKD) suffer from high levels of protein-bound uremic toxins (PBUTs) that contribute to various comorbidities. Conventional dialysis methods are ineffective in removing these PBUTs. A potential solution could be offered by a bioartificial kidney (BAK) composed...

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Autores principales: Faria, João, Ahmed, Sabbir, Stamatialis, Dimitrios, Verhaar, Marianne C., Masereeuw, Rosalinde, Gerritsen, Karin G. F., Mihăilă, Silvia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419568/
https://www.ncbi.nlm.nih.gov/pubmed/37569805
http://dx.doi.org/10.3390/ijms241512435
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author Faria, João
Ahmed, Sabbir
Stamatialis, Dimitrios
Verhaar, Marianne C.
Masereeuw, Rosalinde
Gerritsen, Karin G. F.
Mihăilă, Silvia M.
author_facet Faria, João
Ahmed, Sabbir
Stamatialis, Dimitrios
Verhaar, Marianne C.
Masereeuw, Rosalinde
Gerritsen, Karin G. F.
Mihăilă, Silvia M.
author_sort Faria, João
collection PubMed
description Patients with end-stage kidney disease (ESKD) suffer from high levels of protein-bound uremic toxins (PBUTs) that contribute to various comorbidities. Conventional dialysis methods are ineffective in removing these PBUTs. A potential solution could be offered by a bioartificial kidney (BAK) composed of porous membranes covered by proximal tubule epithelial cells (PTECs) that actively secrete PBUTs. However, BAK development is currently being hampered by a lack of knowledge regarding the cytocompatibility of the dialysis fluid (DF) that comes in contact with the PTECs. Here, we conducted a comprehensive functional assessment of the DF on human conditionally immortalized PTECs (ciPTECs) cultured as monolayers in well plates, on Transwell(®) inserts, or on hollow fiber membranes (HFMs) that form functional units of a BAK. We evaluated cell viability markers, monolayer integrity, and PBUT clearance. Our results show that exposure to DF did not affect ciPTECs’ viability, membrane integrity, or function. Seven anionic PBUTs were efficiently cleared from the perfusion fluid containing a PBUTs cocktail or uremic plasma, an effect which was enhanced in the presence of albumin. Overall, our findings support that the DF is cytocompatible and does not compromise ciPTECs function, paving the way for further advancements in BAK development and its potential clinical application.
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spelling pubmed-104195682023-08-12 Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions Faria, João Ahmed, Sabbir Stamatialis, Dimitrios Verhaar, Marianne C. Masereeuw, Rosalinde Gerritsen, Karin G. F. Mihăilă, Silvia M. Int J Mol Sci Article Patients with end-stage kidney disease (ESKD) suffer from high levels of protein-bound uremic toxins (PBUTs) that contribute to various comorbidities. Conventional dialysis methods are ineffective in removing these PBUTs. A potential solution could be offered by a bioartificial kidney (BAK) composed of porous membranes covered by proximal tubule epithelial cells (PTECs) that actively secrete PBUTs. However, BAK development is currently being hampered by a lack of knowledge regarding the cytocompatibility of the dialysis fluid (DF) that comes in contact with the PTECs. Here, we conducted a comprehensive functional assessment of the DF on human conditionally immortalized PTECs (ciPTECs) cultured as monolayers in well plates, on Transwell(®) inserts, or on hollow fiber membranes (HFMs) that form functional units of a BAK. We evaluated cell viability markers, monolayer integrity, and PBUT clearance. Our results show that exposure to DF did not affect ciPTECs’ viability, membrane integrity, or function. Seven anionic PBUTs were efficiently cleared from the perfusion fluid containing a PBUTs cocktail or uremic plasma, an effect which was enhanced in the presence of albumin. Overall, our findings support that the DF is cytocompatible and does not compromise ciPTECs function, paving the way for further advancements in BAK development and its potential clinical application. MDPI 2023-08-04 /pmc/articles/PMC10419568/ /pubmed/37569805 http://dx.doi.org/10.3390/ijms241512435 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Faria, João
Ahmed, Sabbir
Stamatialis, Dimitrios
Verhaar, Marianne C.
Masereeuw, Rosalinde
Gerritsen, Karin G. F.
Mihăilă, Silvia M.
Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title_full Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title_fullStr Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title_full_unstemmed Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title_short Bioengineered Kidney Tubules Efficiently Clear Uremic Toxins in Experimental Dialysis Conditions
title_sort bioengineered kidney tubules efficiently clear uremic toxins in experimental dialysis conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419568/
https://www.ncbi.nlm.nih.gov/pubmed/37569805
http://dx.doi.org/10.3390/ijms241512435
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