Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10953987 | Journal of Molecular and Cellular Cardiology | 2010 | 9 Pages |
Abstract
⺠Previously, we reported that the autologous administration of bone marrow-derived mesenchymal stem cells (BM-MSC) significantly attenuated myocardial dysfunction and injury in a rat model of acute myocarditis. But BM aspiration procedures are invasive and can yield low numbers of MSC after processing. ⺠In this study, we focused on fetal membranes (FMs) as an alternative source of BM-MSC to provide a large number of cells. ⺠This study showed that the intravenous allogeneic administration of FM-MSC ameliorated cardiac dysfunction in a rat model of acute myocarditis. These beneficial effects may be mainly attributable to the suppression of T-lymphocyte activation rather than to angiogenesis and cardiomyocyte differentiation of the administrated allogeneic FM-MSC. ⺠These results suggest that allogeneic administration of FM-MSC might provide a new therapeutic strategy for the treatment of acute myocarditis.
Keywords
BM-MSCleft ventricular diastolic dimensionLVDsLVSPTGF-β3FMSLVDdMCP1α-MEMMSCHRPGFPPBSFBSFITCH&EEAMα-Minimal essential mediumTransforming growth factor-β3fetal bovine serumImmunosuppressionMesenchymal stem cellsBone marrow-derived mesenchymal stem cellsfetal membranesfetal membraneleft ventricular systolic pressurefluorescein isothiocyanatemajor histocompatibility complexMHCPhosphate-buffered salinebone marrowAcute myocarditisexperimental autoimmune myocarditisHematoxylin and EosinHorseradish peroxidasemonocyte chemoattractant protein 1green fluorescent proteinAllogeneic transplantationaci
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Authors
Shin Ishikane, Kenichi Yamahara, Masaharu Sada, Kazuhiko Harada, Makoto Kodama, Hatsue Ishibashi-Ueda, Kazuhide Hayakawa, Kenichi Mishima, Katsunori Iwasaki, Michihiro Fujiwara, Kenji Kangawa, Tomoaki Ikeda,