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Secretome signature of cardiopoietic cells echoed in rescued infarcted heart proteome

Stem cell paracrine activity is implicated in cardiac repair. Linkage between secretome functionality and therapeutic outcome was here interrogated by systems analytics of biobanked human cardiopoietic cells, a regenerative biologic in advanced clinical trials. Protein chip array identified 155 prot...

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Detalles Bibliográficos
Autores principales: Arrell, D. Kent, Crespo‐Diaz, Ruben J., Yamada, Satsuki, Jeon, Ryounghoon, Garmany, Armin, Park, Sungjo, Adolf, Jeffrey P., Livia, Christopher, Hillestad, Matthew L., Bartunek, Jozef, Behfar, Atta, Terzic, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380441/
https://www.ncbi.nlm.nih.gov/pubmed/34047493
http://dx.doi.org/10.1002/sctm.20-0509
Descripción
Sumario:Stem cell paracrine activity is implicated in cardiac repair. Linkage between secretome functionality and therapeutic outcome was here interrogated by systems analytics of biobanked human cardiopoietic cells, a regenerative biologic in advanced clinical trials. Protein chip array identified 155 proteins differentially secreted by cardiopoietic cells with clinical benefit, expanded into a 520 node network, collectively revealing inherent vasculogenic properties along with cardiac and smooth muscle differentiation and development. Next generation RNA sequencing, refined by pathway analysis, pinpointed miR‐146 dependent regulation upstream of the decoded secretome. Intracellular and extracellular integration unmasked commonality across cardio‐vasculogenic processes. Mirroring the secretome pattern, infarcted hearts benefiting from cardiopoietic cell therapy restored the disease proteome engaging cardiovascular system functions. The cardiopoietic cell secretome thus confers a therapeutic molecular imprint on recipient hearts, with response informed by predictive systems profiling.