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Iron oxide nanoparticle-mediated development of cellular gap junction crosstalk to improve mesenchymal stem cells' therapeutic efficacy for myocardial infarction

 Jin Han  ;  Bokyoung Kim  ;  Jung-Youn Shin  ;  Seungmi Ryu  ;  Myungkyung Noh  ;  Jongsu Woo  ;  Jin-Sil Park  ;  Youjin Lee  ;  Nohyun Lee  ;  Taeghwan Hyeon  ;  Donghoon Choi  ;  Byung-Soo Kim 
 ACS NANO, Vol.9(3) : 2805-2819, 2015 
Journal Title
Issue Date
Animals ; Biological Transport ; Cell Line ; Cell Separation ; Coculture Techniques ; Connexin 43/metabolism ; Ferric Compounds/chemistry* ; Ferric Compounds/metabolism ; Ferric Compounds/pharmacology* ; Gap Junctions/drug effects* ; Gene Expression Regulation/drug effects ; Humans ; Mesenchymal Stem Cell Transplantation* ; Mesenchymal Stromal Cells/cytology* ; Mesenchymal Stromal Cells/drug effects ; Mesenchymal Stromal Cells/metabolism ; Myocardial Infarction/pathology ; Myocardial Infarction/physiopathology ; Myocardial Infarction/surgery* ; Myocardium/metabolism ; Myocardium/pathology ; Nanoparticles* ; Paracrine Communication ; Phenotype ; Rats ; Rats, Sprague-Dawley ; Survival Analysis ; Ventricular Remodeling
ion delivery ; iron oxide nanoparticle ; mesenchymal stem cells ; myocardial infarction ; tissue engineering
Electrophysiological phenotype development and paracrine action of mesenchymal stem cells (MSCs) are the critical factors that determine the therapeutic efficacy of MSCs for myocardial infarction (MI). In such respect, coculture of MSCs with cardiac cells has windowed a platform for cardiac priming of MSCs. Particularly, active gap junctional crosstalk of MSCs with cardiac cells in coculture has been known to play a major role in the MSC modification through coculture. Here, we report that iron oxide nanoparticles (IONPs) significantly augment the expression of connexin 43 (Cx43), a gap junction protein, of cardiomyoblasts (H9C2), which would be critical for gap junctional communication with MSCs in coculture for the generation of therapeutic potential-improved MSCs. MSCs cocultured with IONP-harboring H9C2 (cocultured MSCs: cMSCs) showed active cellular crosstalk with H9C2 and displayed significantly higher levels of electrophysiological cardiac biomarkers and a cardiac repair-favorable paracrine profile, both of which are responsible for MI repair. Accordingly, significantly improved animal survival and heart function were observed upon cMSC injection into rat MI models compared with the injection of unmodified MSCs. The present study highlights an application of IONPs in developing gap junctional crosstalk among the cells and generating cMSCs that exceeds the reparative potentials of conventional MSCs. On the basis of our finding, the potential application of IONPs can be extended in cell biology and stem cell-based therapies.
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1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
Park, Jin Sil(박진실)
Choi, Dong Hoon(최동훈) ORCID logo https://orcid.org/0000-0002-2009-9760
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