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Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes

Crosstalk mechanisms between pericytes, endothelial cells, and astrocytes preserve integrity and function of the blood-brain-barrier (BBB) under physiological conditions. Long intercellular channels allowing the transfer of small molecules and organelles between distant cells called tunneling nanotu...

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Autores principales: Pisani, Francesco, Castagnola, Valentina, Simone, Laura, Loiacono, Fabrizio, Svelto, Maria, Benfenati, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256725/
https://www.ncbi.nlm.nih.gov/pubmed/35790716
http://dx.doi.org/10.1038/s41419-022-05025-y
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author Pisani, Francesco
Castagnola, Valentina
Simone, Laura
Loiacono, Fabrizio
Svelto, Maria
Benfenati, Fabio
author_facet Pisani, Francesco
Castagnola, Valentina
Simone, Laura
Loiacono, Fabrizio
Svelto, Maria
Benfenati, Fabio
author_sort Pisani, Francesco
collection PubMed
description Crosstalk mechanisms between pericytes, endothelial cells, and astrocytes preserve integrity and function of the blood-brain-barrier (BBB) under physiological conditions. Long intercellular channels allowing the transfer of small molecules and organelles between distant cells called tunneling nanotubes (TNT) represent a potential substrate for energy and matter exchanges between the tripartite cellular compartments of the BBB. However, the role of TNT across BBB cells under physiological conditions and in the course of BBB dysfunction is unknown. In this work, we analyzed the TNT’s role in the functional dialog between human brain endothelial cells, and brain pericytes co-cultured with human astrocytes under normal conditions or after exposure to ischemia/reperfusion, a condition in which BBB breakdown occurs, and pericytes participate in the BBB repair. Using live time-lapse fluorescence microscopy and laser-scanning confocal microscopy, we found that astrocytes form long TNT with pericytes and endothelial cells and receive functional mitochondria from both cell types through this mechanism. The mitochondrial transfer also occurred in multicellular assembloids of human BBB that reproduce the three-dimensional architecture of the BBB. Under conditions of ischemia/reperfusion, TNT formation is upregulated, and astrocytes exposed to oxygen-glucose deprivation were rescued from apoptosis by healthy pericytes through TNT-mediated transfer of functional mitochondria, an effect that was virtually abolished in the presence of TNT-destroying drugs. The results establish a functional role of TNT in the crosstalk between BBB cells and demonstrate that TNT-mediated mitochondrial transfer from pericytes rescues astrocytes from ischemia/reperfusion-induced apoptosis. Our data confirm that the pericytes might play a pivotal role in preserving the structural and functional integrity of BBB under physiological conditions and participate in BBB repair in brain diseases. [Image: see text]
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spelling pubmed-92567252022-07-07 Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes Pisani, Francesco Castagnola, Valentina Simone, Laura Loiacono, Fabrizio Svelto, Maria Benfenati, Fabio Cell Death Dis Article Crosstalk mechanisms between pericytes, endothelial cells, and astrocytes preserve integrity and function of the blood-brain-barrier (BBB) under physiological conditions. Long intercellular channels allowing the transfer of small molecules and organelles between distant cells called tunneling nanotubes (TNT) represent a potential substrate for energy and matter exchanges between the tripartite cellular compartments of the BBB. However, the role of TNT across BBB cells under physiological conditions and in the course of BBB dysfunction is unknown. In this work, we analyzed the TNT’s role in the functional dialog between human brain endothelial cells, and brain pericytes co-cultured with human astrocytes under normal conditions or after exposure to ischemia/reperfusion, a condition in which BBB breakdown occurs, and pericytes participate in the BBB repair. Using live time-lapse fluorescence microscopy and laser-scanning confocal microscopy, we found that astrocytes form long TNT with pericytes and endothelial cells and receive functional mitochondria from both cell types through this mechanism. The mitochondrial transfer also occurred in multicellular assembloids of human BBB that reproduce the three-dimensional architecture of the BBB. Under conditions of ischemia/reperfusion, TNT formation is upregulated, and astrocytes exposed to oxygen-glucose deprivation were rescued from apoptosis by healthy pericytes through TNT-mediated transfer of functional mitochondria, an effect that was virtually abolished in the presence of TNT-destroying drugs. The results establish a functional role of TNT in the crosstalk between BBB cells and demonstrate that TNT-mediated mitochondrial transfer from pericytes rescues astrocytes from ischemia/reperfusion-induced apoptosis. Our data confirm that the pericytes might play a pivotal role in preserving the structural and functional integrity of BBB under physiological conditions and participate in BBB repair in brain diseases. [Image: see text] Nature Publishing Group UK 2022-07-05 /pmc/articles/PMC9256725/ /pubmed/35790716 http://dx.doi.org/10.1038/s41419-022-05025-y 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
Pisani, Francesco
Castagnola, Valentina
Simone, Laura
Loiacono, Fabrizio
Svelto, Maria
Benfenati, Fabio
Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title_full Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title_fullStr Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title_full_unstemmed Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title_short Role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
title_sort role of pericytes in blood–brain barrier preservation during ischemia through tunneling nanotubes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256725/
https://www.ncbi.nlm.nih.gov/pubmed/35790716
http://dx.doi.org/10.1038/s41419-022-05025-y
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