Paracrine action accounts for marked protection of ischemic heart by Akt-modified mesenchymal stem cells
By M. Gnecchi, Huamei He, Olin D. Liang, L. Melo, F. Morello, H. Mu, N. Noiseux, Lunan Zhang, R. Pratt, J. Ingwall and 1 more. Nature Medicine, 2005
1,699 citations recorded by the source corpus.
Subfields: Biomaterials, Genetics, Surgery
View Paper: https://www.semanticscholar.org/paper/44630cdb51f90c7da3e39355e71f3057e7ea53ee
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Citations in the corpus
- Harnessing the Mesenchymal Stem Cell Secretome for the Treatment of Cardiovascular Disease (2012, background): “Please refer to the publisher's site for terms of use.”
- Exosome secreted by MSC reduces myocardial ischemia/reperfusion injury. (2010, background): “Recent reports have suggested that some of these reparative effects are mediated by paracrine factors secreted by MSCs (Caplan and Dennis, 2006a; Gnecchi et al., 2005, 2006; Schafer and Northoff, 2008).”
- Reduction of myocardial infarct size by human mesenchymal stem cell conditioned medium. (2008, background): “Recently, it has been demonstrated that rat bone marrow derived MSCs, transduced with the survival gene Akt, can protect ischemic myocardium via their paracrine secretions (Gnecchi et al., 2005).”
- Allogeneic mesenchymal stem cells restore cardiac function in chronic ischemic cardiomyopathy via trilineage differentiating capacity (2009, background): “Many studies have failed to document MSC differentiation into cardiac cell constituents in the infarcted heart (12, 28, 29).”
- Production of De Novo Cardiomyocytes: Human Pluripotent Stem Cell Differentiation and Direct Reprogramming (2012, neutral): “Because these transplanted populations do not generate new cardiomyocytes, the improvement may be due to paracrine effects that lead to enhanced vascularization (Gnecchi et al., 2005).”
- Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts (2007, background): “There is evidence that transplanted cells produce paracrine factors that enhance survival of host cardiomyocytes postinfarctio”
- Exosomes: vehicles of intercellular signaling, biomarkers, and vectors of cell therapy. (2015, neutral): “(73) first proposed that the effect of genetically engineered MSCs takes place in less than 72 h, before any regeneration can take place, and showed that CM from MSCs (MSC-CM) cultured in vitro have efficacy comparable to that of whole-cell transplantation in preventing ventricular remodeling.”
- Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury. (2013, background): “Most studies suggest that MSCs mediate their therapeutic efficacy through the secretion of paracrine factors (Chimenti et al., 2010; Gnecchi et al., 2005, 2006, 2008).”