TY - JOUR
T1 - Cellular Aging Secretes
T2 - a Comparison of Bone-Marrow-Derived and Induced Mesenchymal Stem Cells and Their Secretome Over Long-Term Culture
AU - Marote, Ana
AU - Santos, Diogo
AU - Mendes-Pinheiro, Bárbara
AU - Serre-Miranda, Cláudia
AU - Anjo, Sandra I.
AU - Vieira, Joana
AU - Ferreira-Antunes, Filipa
AU - Correia, Joana Sofia
AU - Borges-Pereira, Caroline
AU - Pinho, Andreia G.
AU - Campos, Jonas
AU - Manadas, Bruno
AU - Teixeira, Manuel R.
AU - Correia-Neves, Margarida
AU - Pinto, Luísa
AU - Costa, Pedro M.
AU - Roybon, Laurent
AU - Salgado, António J.
PY - 2023
Y1 - 2023
N2 - 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. Graphical Abstract: [Figure not available: see fulltext.].
AB - 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. Graphical Abstract: [Figure not available: see fulltext.].
KW - Bone marrow
KW - Human platelet lysate
KW - Induced pluripotent stem cells
KW - Mesenchymal stem cells
KW - Replicative senescence
KW - Secretome
KW - Senescence-associated secretory profile
U2 - 10.1007/s12015-022-10453-6
DO - 10.1007/s12015-022-10453-6
M3 - Article
C2 - 36152233
AN - SCOPUS:85138719382
SN - 2629-3269
VL - 19
SP - 248
EP - 263
JO - Stem Cell Reviews and Reports
JF - Stem Cell Reviews and Reports
IS - 1
ER -