Hemodynamics regulate spatiotemporal artery muscularization in the developing circle of Willis.

artery muscularization brain artery development circle of Willis developmental biology flow hemodynamics vascular smooth muscle cell differentiation zebrafish

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
10 Jul 2024
Historique:
medline: 10 7 2024
pubmed: 10 7 2024
entrez: 10 7 2024
Statut: epublish

Résumé

Vascular smooth muscle cells (VSMCs) envelop vertebrate brain arteries and play a crucial role in regulating cerebral blood flow and neurovascular coupling. The dedifferentiation of VSMCs is implicated in cerebrovascular disease and neurodegeneration. Despite its importance, the process of VSMC differentiation on brain arteries during development remains inadequately characterized. Understanding this process could aid in reprogramming and regenerating dedifferentiated VSMCs in cerebrovascular diseases. In this study, we investigated VSMC differentiation on zebrafish circle of Willis (CoW), comprising major arteries that supply blood to the vertebrate brain. We observed that arterial specification of CoW endothelial cells (ECs) occurs after their migration from cranial venous plexus to form CoW arteries. Subsequently,

Identifiants

pubmed: 38985140
doi: 10.7554/eLife.94094
pii: 94094
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : R01NS109160
Pays : United States
Organisme : NIH HHS
ID : R01DK118728
Pays : United States
Organisme : American Heart Association
ID : AHA23POST1025829

Informations de copyright

© 2024, Cheng, Xia et al.

Déclaration de conflit d'intérêts

SC, IX, RW, JA, AS, SN No competing interests declared

Auteurs

Siyuan Cheng (S)

Department of Genetics, Yale School of Medicine, New Haven, United States.
Yale Cardiovascular Research Center, Section of Cardiology, Department of Internal Medicine, Yale School of Medicine, New Haven, United States.
Vascular Biology & Therapeutics Program, Yale School of Medicine, New Haven, United States.

Ivan Fan Xia (IF)

Department of Genetics, Yale School of Medicine, New Haven, United States.
Yale Cardiovascular Research Center, Section of Cardiology, Department of Internal Medicine, Yale School of Medicine, New Haven, United States.
Vascular Biology & Therapeutics Program, Yale School of Medicine, New Haven, United States.

Renate Wanner (R)

Department of Genetics, Yale School of Medicine, New Haven, United States.
Yale Cardiovascular Research Center, Section of Cardiology, Department of Internal Medicine, Yale School of Medicine, New Haven, United States.
Vascular Biology & Therapeutics Program, Yale School of Medicine, New Haven, United States.

Javier Abello (J)

Department of Cell Biology & Physiology, School of Medicine, Washington University in St. Louis, St. Louis, United States.

Amber N Stratman (AN)

Department of Cell Biology & Physiology, School of Medicine, Washington University in St. Louis, St. Louis, United States.

Stefania Nicoli (S)

Department of Genetics, Yale School of Medicine, New Haven, United States.
Yale Cardiovascular Research Center, Section of Cardiology, Department of Internal Medicine, Yale School of Medicine, New Haven, United States.
Vascular Biology & Therapeutics Program, Yale School of Medicine, New Haven, United States.

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