Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain

Vascular endothelial cells (vECs) in the brain exhibit structural and functional heterogeneity. Fenestrated, permeable brain vasculature mediates neuroendocrine function, body-fluid regulation, and neural immune responses; however, its vascular formation remains poorly understood. Here, we show that...

Full description

Bibliographic Details
Main Authors: Sweta Parab, Rachael E Quick, Ryota L Matsuoka
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/64295
id doaj-450a1ae6471d48f18b9de00f20c2b143
record_format Article
spelling doaj-450a1ae6471d48f18b9de00f20c2b1432021-05-05T22:41:35ZengeLife Sciences Publications LtdeLife2050-084X2021-01-011010.7554/eLife.64295Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brainSweta Parab0https://orcid.org/0000-0002-9932-5117Rachael E Quick1https://orcid.org/0000-0003-2301-7238Ryota L Matsuoka2https://orcid.org/0000-0001-6214-2889Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, United States; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, United StatesDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, United States; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, United StatesDepartment of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, United States; Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, United StatesVascular endothelial cells (vECs) in the brain exhibit structural and functional heterogeneity. Fenestrated, permeable brain vasculature mediates neuroendocrine function, body-fluid regulation, and neural immune responses; however, its vascular formation remains poorly understood. Here, we show that specific combinations of vascular endothelial growth factors (Vegfs) are required to selectively drive fenestrated vessel formation in the zebrafish myelencephalic choroid plexus (mCP). We found that the combined, but not individual, loss of Vegfab, Vegfc, and Vegfd causes severely impaired mCP vascularization with little effect on neighboring non-fenestrated brain vessel formation, demonstrating fenestrated-vEC-specific angiogenic requirements. This Vegfs-mediated vessel-selective patterning also involves Ccbe1. Expression analyses, cell-type-specific ablation, and paracrine activity-deficient vegfc mutant characterization suggest that vEC-autonomous Vegfc and meningeal fibroblast-derived Vegfab and Vegfd are critical for mCP vascularization. These results define molecular cues and cell types critical for directing fenestrated CP vascularization and indicate that vECs’ distinct molecular requirements for angiogenesis underlie brain vessel heterogeneity.https://elifesciences.org/articles/64295choroid plexusangiogenesiscentral nervous systemVegfsgenetic interactionszebrafish
collection DOAJ
language English
format Article
sources DOAJ
author Sweta Parab
Rachael E Quick
Ryota L Matsuoka
spellingShingle Sweta Parab
Rachael E Quick
Ryota L Matsuoka
Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
eLife
choroid plexus
angiogenesis
central nervous system
Vegfs
genetic interactions
zebrafish
author_facet Sweta Parab
Rachael E Quick
Ryota L Matsuoka
author_sort Sweta Parab
title Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
title_short Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
title_full Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
title_fullStr Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
title_full_unstemmed Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
title_sort endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-01-01
description Vascular endothelial cells (vECs) in the brain exhibit structural and functional heterogeneity. Fenestrated, permeable brain vasculature mediates neuroendocrine function, body-fluid regulation, and neural immune responses; however, its vascular formation remains poorly understood. Here, we show that specific combinations of vascular endothelial growth factors (Vegfs) are required to selectively drive fenestrated vessel formation in the zebrafish myelencephalic choroid plexus (mCP). We found that the combined, but not individual, loss of Vegfab, Vegfc, and Vegfd causes severely impaired mCP vascularization with little effect on neighboring non-fenestrated brain vessel formation, demonstrating fenestrated-vEC-specific angiogenic requirements. This Vegfs-mediated vessel-selective patterning also involves Ccbe1. Expression analyses, cell-type-specific ablation, and paracrine activity-deficient vegfc mutant characterization suggest that vEC-autonomous Vegfc and meningeal fibroblast-derived Vegfab and Vegfd are critical for mCP vascularization. These results define molecular cues and cell types critical for directing fenestrated CP vascularization and indicate that vECs’ distinct molecular requirements for angiogenesis underlie brain vessel heterogeneity.
topic choroid plexus
angiogenesis
central nervous system
Vegfs
genetic interactions
zebrafish
url https://elifesciences.org/articles/64295
work_keys_str_mv AT swetaparab endothelialcelltypespecificmolecularrequirementsforangiogenesisdrivefenestratedvesseldevelopmentinthebrain
AT rachaelequick endothelialcelltypespecificmolecularrequirementsforangiogenesisdrivefenestratedvesseldevelopmentinthebrain
AT ryotalmatsuoka endothelialcelltypespecificmolecularrequirementsforangiogenesisdrivefenestratedvesseldevelopmentinthebrain
_version_ 1721457616421388288