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                  <mods:namePart>Esteve Codina, Anna</mods:namePart>
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                  <mods:namePart>Arribas, Víctor</mods:namePart>
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                  <mods:namePart>Onetti, Yara</mods:namePart>
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                  <mods:namePart>Ramiro Pareta, Marina</mods:namePart>
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                  <mods:namePart>Villacampa, Pilar</mods:namePart>
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                  <mods:namePart>Beck, Heike</mods:namePart>
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                  <mods:namePart>Merkel, Angelika</mods:namePart>
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                  <mods:namePart>Sperandio, Markus</mods:namePart>
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                  <mods:namePart>Martínez Estrada, Ofelia María</mods:namePart>
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                  <mods:namePart>Schmid, Bettina</mods:namePart>
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                  <mods:namePart>Montañez, Eloi</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2024-06-04T18:07:25Z2024-06-04T18:07:25Z2024-02-012024-06-04T18:07:30Z</mods:dateIssued>
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               <mods:abstract>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.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">(c) American Society for Clinical Investigation, 2024 info:eu-repo/semantics/openAccess</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Endoteli</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Angiogènesi</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Animals</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Proteïnes</mods:topic>
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               <mods:subject>
                  <mods:topic>Endothelium</mods:topic>
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               <mods:subject>
                  <mods:topic>Neovascularization</mods:topic>
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               <mods:subject>
                  <mods:topic>Animals</mods:topic>
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               <mods:subject>
                  <mods:topic>Proteins</mods:topic>
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                  <mods:title>Endothelial TDP-43 controls sprouting angiogenesis and vascular barrier integrity, and its deletion triggers neuroinflammation</mods:title>
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