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               <dc:title>Endothelial TDP-43 controls sprouting angiogenesis and vascular barrier integrity, and its deletion triggers neuroinflammation</dc:title>
               <dc:creator>Esteve Codina, Anna</dc:creator>
               <dc:creator>Arribas, Víctor</dc:creator>
               <dc:creator>Onetti, Yara</dc:creator>
               <dc:creator>Ramiro Pareta, Marina</dc:creator>
               <dc:creator>Villacampa, Pilar</dc:creator>
               <dc:creator>Beck, Heike</dc:creator>
               <dc:creator>Alberola, Mariona</dc:creator>
               <dc:creator>Merkel, Angelika</dc:creator>
               <dc:creator>Sperandio, Markus</dc:creator>
               <dc:creator>Martínez Estrada, Ofelia María</dc:creator>
               <dc:creator>Schmid, Bettina</dc:creator>
               <dc:creator>Montañez, Eloi</dc:creator>
               <dc:subject>Endoteli</dc:subject>
               <dc:subject>Angiogènesi</dc:subject>
               <dc:subject>Animals</dc:subject>
               <dc:subject>Proteïnes</dc:subject>
               <dc:subject>Endothelium</dc:subject>
               <dc:subject>Neovascularization</dc:subject>
               <dc:subject>Animals</dc:subject>
               <dc:subject>Proteins</dc:subject>
               <dc:description>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.</dc:description>
               <dc:date>2024-06-04T18:07:25Z</dc:date>
               <dc:date>2024-06-04T18:07:25Z</dc:date>
               <dc:date>2024-02-01</dc:date>
               <dc:date>2024-06-04T18:07:30Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1172/jci.insight.177819</dc:relation>
               <dc:relation>JCI Insight, 2024, vol. 9, num.5</dc:relation>
               <dc:relation>https://doi.org/10.1172/jci.insight.177819</dc:relation>
               <dc:rights>(c) American Society for Clinical Investigation, 2024</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>American Society for Clinical Investigation</dc:publisher>
               <dc:source>Articles publicats en revistes (Ciències Fisiològiques)</dc:source>
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