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Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier
Microvascular basement membrane (BM) plays a pivotal role in the interactions of astrocyte with endothelium to maintain the blood–brain barrier (BBB) homeostasis; however, the significance and precise regulation of the endothelial cell–derived BM component in the BBB remain incompletely understood....
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067974/ https://www.ncbi.nlm.nih.gov/pubmed/36995368 http://dx.doi.org/10.1083/jcb.202103098 |
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author | Liu, Hui Wei, Jia-Yi Li, Yuan Ban, Meng Sun, Qi Wang, Hui-Jie Zhao, Dan Tong, Pai-Ge Wang, Li Wang, Kang-Ji Yue, Jin-Li Zhang, Hong-Yan Fang, Wen-Gang Liu, Dong-Xin Shang, De-Shu Li, Bo Jin, Ya-Ping Cao, Liu Zhao, Wei-Dong Chen, Yu-Hua |
author_facet | Liu, Hui Wei, Jia-Yi Li, Yuan Ban, Meng Sun, Qi Wang, Hui-Jie Zhao, Dan Tong, Pai-Ge Wang, Li Wang, Kang-Ji Yue, Jin-Li Zhang, Hong-Yan Fang, Wen-Gang Liu, Dong-Xin Shang, De-Shu Li, Bo Jin, Ya-Ping Cao, Liu Zhao, Wei-Dong Chen, Yu-Hua |
author_sort | Liu, Hui |
collection | PubMed |
description | Microvascular basement membrane (BM) plays a pivotal role in the interactions of astrocyte with endothelium to maintain the blood–brain barrier (BBB) homeostasis; however, the significance and precise regulation of the endothelial cell–derived BM component in the BBB remain incompletely understood. Here, we report that conditional knockout of Atg7 in endothelial cells (Atg7-ECKO) leads to astrocyte–microvascular disassociation in the brain. Our results reveal astrocytic endfeet detachment from microvessels and BBB leakage in Atg7-ECKO mice. Furthermore, we find that the absence of endothelial Atg7 downregulates the expression of fibronectin, a major BM component of the BBB, causing significantly reduced coverage of astrocytes along cerebral microvessels. We reveal Atg7 triggers the expression of endothelial fibronectin via regulating PKA activity to affect the phosphorylation of cAMP-responsive element-binding protein. These results suggest that Atg7-regulated endothelial fibronectin production is required for astrocytes adhesion to microvascular wall for maintaining the BBB homeostasis. Thus, endothelial Atg7 plays an essential role in astrocyte–endothelium interactions to maintain the BBB integrity. |
format | Online Article Text |
id | pubmed-10067974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100679742023-09-30 Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier Liu, Hui Wei, Jia-Yi Li, Yuan Ban, Meng Sun, Qi Wang, Hui-Jie Zhao, Dan Tong, Pai-Ge Wang, Li Wang, Kang-Ji Yue, Jin-Li Zhang, Hong-Yan Fang, Wen-Gang Liu, Dong-Xin Shang, De-Shu Li, Bo Jin, Ya-Ping Cao, Liu Zhao, Wei-Dong Chen, Yu-Hua J Cell Biol Article Microvascular basement membrane (BM) plays a pivotal role in the interactions of astrocyte with endothelium to maintain the blood–brain barrier (BBB) homeostasis; however, the significance and precise regulation of the endothelial cell–derived BM component in the BBB remain incompletely understood. Here, we report that conditional knockout of Atg7 in endothelial cells (Atg7-ECKO) leads to astrocyte–microvascular disassociation in the brain. Our results reveal astrocytic endfeet detachment from microvessels and BBB leakage in Atg7-ECKO mice. Furthermore, we find that the absence of endothelial Atg7 downregulates the expression of fibronectin, a major BM component of the BBB, causing significantly reduced coverage of astrocytes along cerebral microvessels. We reveal Atg7 triggers the expression of endothelial fibronectin via regulating PKA activity to affect the phosphorylation of cAMP-responsive element-binding protein. These results suggest that Atg7-regulated endothelial fibronectin production is required for astrocytes adhesion to microvascular wall for maintaining the BBB homeostasis. Thus, endothelial Atg7 plays an essential role in astrocyte–endothelium interactions to maintain the BBB integrity. Rockefeller University Press 2023-03-30 /pmc/articles/PMC10067974/ /pubmed/36995368 http://dx.doi.org/10.1083/jcb.202103098 Text en © 2023 Liu et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Liu, Hui Wei, Jia-Yi Li, Yuan Ban, Meng Sun, Qi Wang, Hui-Jie Zhao, Dan Tong, Pai-Ge Wang, Li Wang, Kang-Ji Yue, Jin-Li Zhang, Hong-Yan Fang, Wen-Gang Liu, Dong-Xin Shang, De-Shu Li, Bo Jin, Ya-Ping Cao, Liu Zhao, Wei-Dong Chen, Yu-Hua Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title | Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title_full | Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title_fullStr | Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title_full_unstemmed | Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title_short | Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
title_sort | endothelial depletion of atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067974/ https://www.ncbi.nlm.nih.gov/pubmed/36995368 http://dx.doi.org/10.1083/jcb.202103098 |
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