Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm

Abstract Subarachnoid hemorrhage being the rupture of intracranial aneurysm (IA) as a major cause has quite poor prognosis, despite the modern technical advances. Thereby, the mechanisms underlying the rupture of lesions should be clarified. Recently, we and others have clarified the formation of va...

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Main Authors: Isao Ono, Tomomichi Kayahara, Akitsugu Kawashima, Akihiro Okada, Susumu Miyamoto, Hiroharu Kataoka, Hiroki Kurita, Akira Ishii, Tomohiro Aoki
Format: Article
Language:English
Published: Nature Portfolio 2023-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-32001-z
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author Isao Ono
Tomomichi Kayahara
Akitsugu Kawashima
Akihiro Okada
Susumu Miyamoto
Hiroharu Kataoka
Hiroki Kurita
Akira Ishii
Tomohiro Aoki
author_facet Isao Ono
Tomomichi Kayahara
Akitsugu Kawashima
Akihiro Okada
Susumu Miyamoto
Hiroharu Kataoka
Hiroki Kurita
Akira Ishii
Tomohiro Aoki
author_sort Isao Ono
collection DOAJ
description Abstract Subarachnoid hemorrhage being the rupture of intracranial aneurysm (IA) as a major cause has quite poor prognosis, despite the modern technical advances. Thereby, the mechanisms underlying the rupture of lesions should be clarified. Recently, we and others have clarified the formation of vasa vasorum in IA lesions presumably for inflammatory cells to infiltrate in lesions as the potential histopathological alternation leading to rupture. In the present study, we clarified the origin of vasa vasorum as arteries located at the brain surface using 3D-immunohistochemistry with tissue transparency. Using Hypoxyprobe, we then found the presence of hypoxic microenvironment mainly at the adventitia of intracranial arteries where IA is formed. In addition, the production of vascular endothelial growth factor (VEGF) from cultured macrophages in such a hypoxic condition was identified. Furthermore, we found the accumulation of VEGF both in rupture-prone IA lesions induced in a rat model and human unruptured IA lesions. Finally, the VEGF-dependent induction of neovessels from arteries on brain surface was confirmed. The findings from the present study have revealed the potential role of hypoxic microenvironment and hypoxia-induced VEGF production as a machinery triggering rupture of IAs via providing root for inflammatory cells in lesions to exacerbate inflammation.
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spelling doaj.art-c825276e6b4e407fade85041438b83f92023-04-09T11:14:13ZengNature PortfolioScientific Reports2045-23222023-04-0113111210.1038/s41598-023-32001-zHypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysmIsao Ono0Tomomichi Kayahara1Akitsugu Kawashima2Akihiro Okada3Susumu Miyamoto4Hiroharu Kataoka5Hiroki Kurita6Akira Ishii7Tomohiro Aoki8Department of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular CenterDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular CenterDepartment of Neurosurgery, Tokyo Women’s Medical University Yachiyo Medical CenterDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular CenterDepartment of Neurosurgery, Kyoto University Graduate School of MedicineDepartment of Neurosurgery, National Cerebral and Cardiovascular CenterDepartment of Cerebrovascular Surgery, Saitama Medical University International Medical CenterDepartment of Neurosurgery, Kyoto University Graduate School of MedicineDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular CenterAbstract Subarachnoid hemorrhage being the rupture of intracranial aneurysm (IA) as a major cause has quite poor prognosis, despite the modern technical advances. Thereby, the mechanisms underlying the rupture of lesions should be clarified. Recently, we and others have clarified the formation of vasa vasorum in IA lesions presumably for inflammatory cells to infiltrate in lesions as the potential histopathological alternation leading to rupture. In the present study, we clarified the origin of vasa vasorum as arteries located at the brain surface using 3D-immunohistochemistry with tissue transparency. Using Hypoxyprobe, we then found the presence of hypoxic microenvironment mainly at the adventitia of intracranial arteries where IA is formed. In addition, the production of vascular endothelial growth factor (VEGF) from cultured macrophages in such a hypoxic condition was identified. Furthermore, we found the accumulation of VEGF both in rupture-prone IA lesions induced in a rat model and human unruptured IA lesions. Finally, the VEGF-dependent induction of neovessels from arteries on brain surface was confirmed. The findings from the present study have revealed the potential role of hypoxic microenvironment and hypoxia-induced VEGF production as a machinery triggering rupture of IAs via providing root for inflammatory cells in lesions to exacerbate inflammation.https://doi.org/10.1038/s41598-023-32001-z
spellingShingle Isao Ono
Tomomichi Kayahara
Akitsugu Kawashima
Akihiro Okada
Susumu Miyamoto
Hiroharu Kataoka
Hiroki Kurita
Akira Ishii
Tomohiro Aoki
Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
Scientific Reports
title Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
title_full Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
title_fullStr Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
title_full_unstemmed Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
title_short Hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
title_sort hypoxic microenvironment as a crucial factor triggering events leading to rupture of intracranial aneurysm
url https://doi.org/10.1038/s41598-023-32001-z
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