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                  <mods:namePart>Bonilla, Pablo</mods:namePart>
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                  <mods:namePart>Hernández Martín, Joaquim</mods:namePart>
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                  <mods:namePart>Giraldo, Esther</mods:namePart>
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                  <mods:namePart>González-Pérez, Miguel A.</mods:namePart>
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                  <mods:namePart>Alastrue-Agudo, Ana</mods:namePart>
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                  <mods:namePart>Elkhenany, Hoda</mods:namePart>
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                  <mods:namePart>Vicent, María J.</mods:namePart>
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                  <mods:namePart>Navarro, X. (Xavier)</mods:namePart>
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                  <mods:namePart>Edel, Michael J.</mods:namePart>
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                  <mods:namePart>Moreno-Manzano, Victoria</mods:namePart>
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               <mods:abstract>Altres ajuts: Fundació Marató TV3 2017/refs.20172230, 20172231 i 20172110We currently lack effective treatments for the devastating loss of neural function associated with spinal cord injury (SCI). In this study, we evaluated a combination therapy comprising human neural stem cells derived from induced pluripotent stem cells (iPSC-NSC), human mesen-chymal stem cells (MSC), and a pH-responsive polyacetal-curcumin nanoconjugate (PA-C) that al-lows the sustained release of curcumin. In vitro analysis demonstrated that PA-C treatment pro-tected iPSC-NSC from oxidative damage in vitro, while MSC co-culture prevented lipopolysaccha-ride-induced activation of nuclear factor-κB (NF-κB) in iPSC-NSC. Then, we evaluated the combination of PA-C delivery into the intrathecal space in a rat model of contusive SCI with stem cell transplantation. While we failed to observe significant improvements in locomotor function (BBB scale) in treated animals, histological analysis revealed that PA-C-treated or PA-C and iPSC-NSC + MSC-treated animals displayed significantly smaller scars, while PA-C and iPSC-NSC + MSC treatment induced the preservation of β-III Tubulin-positive axons. iPSC-NSC + MSC transplantation fostered the preservation of motoneurons and myelinated tracts, while PA-C treatment polarized microglia into an anti-inflammatory phenotype. Overall, the combination of stem cell transplantation and PA-C treatment confers higher neuroprotective effects compared to individual treatments.</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Spinal cord injury</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Stem cells</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Curcumin</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Neuroprotection</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Polymer-drug conjugate</mods:topic>
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                  <mods:title>Human-induced neural and mesenchymal stem cell therapy combined with a curcumin nanoconjugate as a spinal cord injury treatment</mods:title>
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