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Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport
Next to the skin, the peritoneum is the largest human organ, essentially involved in abdominal health and disease states, but information on peritoneal paracellular tight junctions and transcellular channels and transporters relative to peritoneal transmembrane transport is scant. We studied their p...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575882/ https://www.ncbi.nlm.nih.gov/pubmed/37833387 http://dx.doi.org/10.1038/s41598-023-44466-z |
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author | Levai, Eszter Marinovic, Iva Bartosova, Maria Zhang, Conghui Schaefer, Betti Jenei, Hanna Du, Zhiwei Drozdz, Dorota Klaus, Günter Arbeiter, Klaus Romero, Philipp Schwenger, Vedat Schwab, Constantin Szabo, Attila J. Zarogiannis, Sotirios G. Schmitt, Claus Peter |
author_facet | Levai, Eszter Marinovic, Iva Bartosova, Maria Zhang, Conghui Schaefer, Betti Jenei, Hanna Du, Zhiwei Drozdz, Dorota Klaus, Günter Arbeiter, Klaus Romero, Philipp Schwenger, Vedat Schwab, Constantin Szabo, Attila J. Zarogiannis, Sotirios G. Schmitt, Claus Peter |
author_sort | Levai, Eszter |
collection | PubMed |
description | Next to the skin, the peritoneum is the largest human organ, essentially involved in abdominal health and disease states, but information on peritoneal paracellular tight junctions and transcellular channels and transporters relative to peritoneal transmembrane transport is scant. We studied their peritoneal localization and quantity by immunohistochemistry and confocal microscopy in health, in chronic kidney disease (CKD) and on peritoneal dialysis (PD), with the latter allowing for functional characterizations, in a total of 93 individuals (0–75 years). Claudin-1 to -5, and -15, zonula occludens-1, occludin and tricellulin, SGLT1, PiT1/SLC20A1 and ENaC were consistently detected in mesothelial and arteriolar endothelial cells, with age dependent differences for mesothelial claudin-1 and arteriolar claudin-2/3. In CKD mesothelial claudin-1 and arteriolar claudin-2 and -3 were more abundant. Peritonea from PD patients exhibited increased mesothelial and arteriolar claudin-1 and mesothelial claudin-2 abundance and reduced mesothelial and arteriolar claudin-3 and arteriolar ENaC. Transperitoneal creatinine and glucose transport correlated with pore forming arteriolar claudin-2 and mesothelial claudin-4/-15, and creatinine transport with mesothelial sodium/phosphate cotransporter PiT1/SLC20A1. In multivariable analysis, claudin-2 independently predicted the peritoneal transport rates. In conclusion, tight junction, transcellular transporter and channel proteins are consistently expressed in peritoneal mesothelial and endothelial cells with minor variations across age groups, specific modifications by CKD and PD and distinct associations with transperitoneal creatinine and glucose transport rates. The latter deserve experimental studies to demonstrate mechanistic links. Clinical Trial registration: The study was performed according to the Declaration of Helsinki and is registered at www.clinicaltrials.gov (NCT01893710). |
format | Online Article Text |
id | pubmed-10575882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105758822023-10-15 Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport Levai, Eszter Marinovic, Iva Bartosova, Maria Zhang, Conghui Schaefer, Betti Jenei, Hanna Du, Zhiwei Drozdz, Dorota Klaus, Günter Arbeiter, Klaus Romero, Philipp Schwenger, Vedat Schwab, Constantin Szabo, Attila J. Zarogiannis, Sotirios G. Schmitt, Claus Peter Sci Rep Article Next to the skin, the peritoneum is the largest human organ, essentially involved in abdominal health and disease states, but information on peritoneal paracellular tight junctions and transcellular channels and transporters relative to peritoneal transmembrane transport is scant. We studied their peritoneal localization and quantity by immunohistochemistry and confocal microscopy in health, in chronic kidney disease (CKD) and on peritoneal dialysis (PD), with the latter allowing for functional characterizations, in a total of 93 individuals (0–75 years). Claudin-1 to -5, and -15, zonula occludens-1, occludin and tricellulin, SGLT1, PiT1/SLC20A1 and ENaC were consistently detected in mesothelial and arteriolar endothelial cells, with age dependent differences for mesothelial claudin-1 and arteriolar claudin-2/3. In CKD mesothelial claudin-1 and arteriolar claudin-2 and -3 were more abundant. Peritonea from PD patients exhibited increased mesothelial and arteriolar claudin-1 and mesothelial claudin-2 abundance and reduced mesothelial and arteriolar claudin-3 and arteriolar ENaC. Transperitoneal creatinine and glucose transport correlated with pore forming arteriolar claudin-2 and mesothelial claudin-4/-15, and creatinine transport with mesothelial sodium/phosphate cotransporter PiT1/SLC20A1. In multivariable analysis, claudin-2 independently predicted the peritoneal transport rates. In conclusion, tight junction, transcellular transporter and channel proteins are consistently expressed in peritoneal mesothelial and endothelial cells with minor variations across age groups, specific modifications by CKD and PD and distinct associations with transperitoneal creatinine and glucose transport rates. The latter deserve experimental studies to demonstrate mechanistic links. Clinical Trial registration: The study was performed according to the Declaration of Helsinki and is registered at www.clinicaltrials.gov (NCT01893710). Nature Publishing Group UK 2023-10-13 /pmc/articles/PMC10575882/ /pubmed/37833387 http://dx.doi.org/10.1038/s41598-023-44466-z Text en © The Author(s) 2023 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 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/) . |
spellingShingle | Article Levai, Eszter Marinovic, Iva Bartosova, Maria Zhang, Conghui Schaefer, Betti Jenei, Hanna Du, Zhiwei Drozdz, Dorota Klaus, Günter Arbeiter, Klaus Romero, Philipp Schwenger, Vedat Schwab, Constantin Szabo, Attila J. Zarogiannis, Sotirios G. Schmitt, Claus Peter Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title | Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title_full | Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title_fullStr | Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title_full_unstemmed | Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title_short | Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
title_sort | human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575882/ https://www.ncbi.nlm.nih.gov/pubmed/37833387 http://dx.doi.org/10.1038/s41598-023-44466-z |
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