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               <dc:title>Wharton's jelly mesenchymal stromal cells and derived extracellular vesicles as post-myocardial infarction therapeutic toolkit : an experienced view</dc:title>
               <dc:creator>Muñoz-Domínguez, Noelia</dc:creator>
               <dc:creator>Roura, Santiago</dc:creator>
               <dc:creator>Prat-Vidal, Cristina</dc:creator>
               <dc:creator>Vives Armengol, Joaquim</dc:creator>
               <dc:creator>Universitat Autònoma de Barcelona</dc:creator>
               <dc:subject>Biomanufacturing</dc:subject>
               <dc:subject>Cardiac tissue engineering</dc:subject>
               <dc:subject>Clinical translation</dc:subject>
               <dc:subject>Extracellular vesicles</dc:subject>
               <dc:subject>Mesenchymal stromal cells</dc:subject>
               <dc:subject>Myocardial infarction</dc:subject>
               <dc:subject>Wharton's jelly</dc:subject>
               <dc:description>Outstanding progress has been achieved in developing therapeutic options for reasonably alleviating symptoms and prolonging the lifespan of patients suffering from myocardial infarction (MI). Current treatments, however, only partially address the functional recovery of post-infarcted myocardium, which is in fact the major goal for effective primary care. In this context, we largely investigated novel cell and TE tissue engineering therapeutic approaches for cardiac repair, particu-larly using multipotent mesenchymal stromal cells (MSC) and natural extracellular matrices, from pre-clinical studies to clinical application. A further step in this field is offered by MSC-derived extracellular vesicles (EV), which are naturally released nanosized lipid bilayer-delimited particles with a key role in cell-to-cell communication. Herein, in this review, we further describe and discuss the rationale, outcomes and challenges of our evidence-based therapy approaches using Wharton's jelly MSC and derived EV in post-MI management.</dc:description>
               <dc:date>2021</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>Instituto de Salud Carlos III PI18/00256</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI18/01227</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI19/01788</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI17/01487</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PIC18/00014</dc:relation>
               <dc:relation>Instituto de Salud Carlos III ICI19/00039</dc:relation>
               <dc:relation>Instituto de Salud Carlos III ICI20/00135</dc:relation>
               <dc:relation>Agencia Estatal de Investigación PID2019-110137RB-I00</dc:relation>
               <dc:relation>Agencia Estatal de Investigación SAF2017-84324-C2-1-R</dc:relation>
               <dc:relation>Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-483</dc:relation>
               <dc:relation>Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-719</dc:relation>
               <dc:relation>Agència de Gestió d'Ajuts Universitaris i de Recerca 2019PROD00122</dc:relation>
               <dc:relation>Pharmaceutics ; Vol. 13 Núm. 9 (september 2021), p. 1336</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>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.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
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