Endothelial TDP-43 controls sprouting angiogenesis and vascular barrier integrity, and its deletion triggers neuroinflammation

TAR DNA-binding protein 43 (TDP-43) is a DNA/RNA-binding protein that regulates gene expression, and its malfunction in neurons has been causally associated with multiple neurodegenerative disorders. Although progress has been made in understanding the functions of TDP-43 in neurons, little is known...

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Detalles Bibliográficos
Autores: Arribas, Víctor, Onetti Vilalta, Yara, Ramiro Pareta, Marina|||0000-0002-9017-4981, Villacampa, Pilar|||0000-0002-2860-7475, Beck, Heike, Alberola, Mariona, Esteve-Codina, Anna|||0000-0003-0361-2873, Merkel, Angelika|||0000-0001-5164-6803, Sperandio, Markus|||0000-0002-7689-3613, Martínez-Estrada, Ofelia M.|||0000-0002-1814-1974, Schmid, Bettina, Montanez, Eloi|||0000-0003-4059-5056
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:301940
Acceso en línea:https://ddd.uab.cat/record/301940
https://dx.doi.org/urn:doi:10.1172/jci.insight.177819
Access Level:acceso abierto
Palabra clave:Angiogenesis
Animals
DNA-Binding Proteins
Endothelial Cells
Mice
Neovascularization, Physiologic
Neuroinflammatory Diseases
Descripción
Sumario:TAR DNA-binding protein 43 (TDP-43) is a DNA/RNA-binding protein that regulates gene expression, and its malfunction in neurons has been causally associated with multiple neurodegenerative disorders. Although progress has been made in understanding the functions of TDP-43 in neurons, little is known about its roles in endothelial cells (ECs), angiogenesis, and vascular function. Using inducible EC-specific TDP-43-KO mice, we showed that TDP-43 is required for sprouting angiogenesis, vascular barrier integrity, and blood vessel stability. Postnatal EC-specific deletion of TDP-43 led to retinal hypovascularization due to defects in vessel sprouting associated with reduced EC proliferation and migration. In mature blood vessels, loss of TDP-43 disrupted the blood-brain barrier and triggered vascular degeneration. These vascular defects were associated with an inflammatory response in the CNS with activation of microglia and astrocytes. Mechanistically, deletion of TDP-43 disrupted the fibronectin matrix around sprouting vessels and reduced β-catenin signaling in ECs. Together, our results indicate that TDP-43 is essential for the formation of a stable and mature vasculature.