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Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner

Dysfunctional and leaky blood vessels resulting from disruption of the endothelial cell (EC) barrier accompanies numerous diseases. The EC barrier is established through endothelial cell tight and adherens junctions. However, the expression pattern and precise contribution of different junctional pr...

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Autores principales: Richards, Mark, Nwadozi, Emmanuel, Pal, Sagnik, Martinsson, Pernilla, Kaakinen, Mika, Gloger, Marleen, Sjöberg, Elin, Koltowska, Katarzyna, Betsholtz, Christer, Eklund, Lauri, Nordling, Sofia, Claesson-Welsh, Lena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348850/
https://www.ncbi.nlm.nih.gov/pubmed/35861713
http://dx.doi.org/10.7554/eLife.78517
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author Richards, Mark
Nwadozi, Emmanuel
Pal, Sagnik
Martinsson, Pernilla
Kaakinen, Mika
Gloger, Marleen
Sjöberg, Elin
Koltowska, Katarzyna
Betsholtz, Christer
Eklund, Lauri
Nordling, Sofia
Claesson-Welsh, Lena
author_facet Richards, Mark
Nwadozi, Emmanuel
Pal, Sagnik
Martinsson, Pernilla
Kaakinen, Mika
Gloger, Marleen
Sjöberg, Elin
Koltowska, Katarzyna
Betsholtz, Christer
Eklund, Lauri
Nordling, Sofia
Claesson-Welsh, Lena
author_sort Richards, Mark
collection PubMed
description Dysfunctional and leaky blood vessels resulting from disruption of the endothelial cell (EC) barrier accompanies numerous diseases. The EC barrier is established through endothelial cell tight and adherens junctions. However, the expression pattern and precise contribution of different junctional proteins to the EC barrier is poorly understood. Here, we focus on organs with continuous endothelium to identify structural and functional in vivo characteristics of the EC barrier. Assembly of multiple single-cell RNAseq datasets into a single integrated database revealed the variability and commonalities of EC barrier patterning. Across tissues, Claudin5 exhibited diminishing expression along the arteriovenous axis, correlating with EC barrier integrity. Functional analysis identified tissue-specific differences in leakage properties and response to the leakage agonist histamine. Loss of Claudin5 enhanced histamine-induced leakage in an organotypic and vessel type-specific manner in an inducible, EC-specific, knock-out mouse. Mechanistically, Claudin5 loss left junction ultrastructure unaffected but altered its composition, with concomitant loss of zonula occludens-1 and upregulation of VE-Cadherin expression. These findings uncover the organ-specific organisation of the EC barrier and distinct importance of Claudin5 in different vascular beds, providing insights to modify EC barrier stability in a targeted, organ-specific manner.
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spelling pubmed-93488502022-08-04 Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner Richards, Mark Nwadozi, Emmanuel Pal, Sagnik Martinsson, Pernilla Kaakinen, Mika Gloger, Marleen Sjöberg, Elin Koltowska, Katarzyna Betsholtz, Christer Eklund, Lauri Nordling, Sofia Claesson-Welsh, Lena eLife Cell Biology Dysfunctional and leaky blood vessels resulting from disruption of the endothelial cell (EC) barrier accompanies numerous diseases. The EC barrier is established through endothelial cell tight and adherens junctions. However, the expression pattern and precise contribution of different junctional proteins to the EC barrier is poorly understood. Here, we focus on organs with continuous endothelium to identify structural and functional in vivo characteristics of the EC barrier. Assembly of multiple single-cell RNAseq datasets into a single integrated database revealed the variability and commonalities of EC barrier patterning. Across tissues, Claudin5 exhibited diminishing expression along the arteriovenous axis, correlating with EC barrier integrity. Functional analysis identified tissue-specific differences in leakage properties and response to the leakage agonist histamine. Loss of Claudin5 enhanced histamine-induced leakage in an organotypic and vessel type-specific manner in an inducible, EC-specific, knock-out mouse. Mechanistically, Claudin5 loss left junction ultrastructure unaffected but altered its composition, with concomitant loss of zonula occludens-1 and upregulation of VE-Cadherin expression. These findings uncover the organ-specific organisation of the EC barrier and distinct importance of Claudin5 in different vascular beds, providing insights to modify EC barrier stability in a targeted, organ-specific manner. eLife Sciences Publications, Ltd 2022-07-21 /pmc/articles/PMC9348850/ /pubmed/35861713 http://dx.doi.org/10.7554/eLife.78517 Text en © 2022, Richards et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Richards, Mark
Nwadozi, Emmanuel
Pal, Sagnik
Martinsson, Pernilla
Kaakinen, Mika
Gloger, Marleen
Sjöberg, Elin
Koltowska, Katarzyna
Betsholtz, Christer
Eklund, Lauri
Nordling, Sofia
Claesson-Welsh, Lena
Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title_full Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title_fullStr Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title_full_unstemmed Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title_short Claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
title_sort claudin5 protects the peripheral endothelial barrier in an organ and vessel-type-specific manner
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348850/
https://www.ncbi.nlm.nih.gov/pubmed/35861713
http://dx.doi.org/10.7554/eLife.78517
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