| Literature DB >> 36152233 |
Ana Marote1,2, Diogo Santos3,4, Bárbara Mendes-Pinheiro3,4, Cláudia Serre-Miranda3,4, Sandra I Anjo5,6, Joana Vieira7,8, Filipa Ferreira-Antunes3,4, Joana Sofia Correia3,4, Caroline Borges-Pereira3,4, Andreia G Pinho3,4, Jonas Campos3,4, Bruno Manadas5, Manuel R Teixeira7,8,9, Margarida Correia-Neves3,4, Luísa Pinto3,4,10, Pedro M Costa11, Laurent Roybon12,13,14, António J Salgado3,4.
Abstract
Mesenchymal stem cells (MSCs) hold promising therapeutic potential in several clinical applications, mainly due to their paracrine activity. The implementation of future secretome-based therapeutic strategies requires the use of easily accessible MSCs sources that provide high numbers of cells with homogenous characteristics. MSCs obtained from induced pluripotent stem cells (iMSCs) have been put forward as an advantageous alternative to the gold-standard tissue sources, such as bone marrow (BM-MSCs). In this study, we aimed at comparing the secretome of BM-MSCs and iMSCs over long-term culture. For that, we performed a broad characterization of both sources regarding their identity, proteomic secretome analysis, as well as replicative senescence and associated phenotypes, including its effects on MSCs secretome composition and immunomodulatory action. Our results evidence a rejuvenated phenotype of iMSCs, which is translated into a superior proliferative capacity before the induction of replicative senescence. Despite this significant difference between iMSCs and BM-MSCs proliferation, both untargeted and targeted proteomic analysis revealed a similar secretome composition for both sources in pre-senescent and senescent states. These results suggest that shifting from the use of BM-MSCs to a more advantageous source, like iMSCs, may yield similar therapeutic effects as identified over the past years for this gold-standard MSC source.Entities:
Keywords: Bone marrow; Human platelet lysate; Induced pluripotent stem cells; Mesenchymal stem cells; Replicative senescence; Secretome; Senescence-associated secretory profile
Year: 2022 PMID: 36152233 DOI: 10.1007/s12015-022-10453-6
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 6.692