Dual-modal tracking of transplanted mesenchymal stem cells after myocardial infarction

被引:25
作者
Li, Yefei [1 ]
Yao, Yuyu [1 ]
Sheng, Zulong [1 ]
Yang, Yanxiaoxiao [1 ]
Ma, Genshan [1 ]
机构
[1] Southeast Univ, Dept Cardiol, Zhongda Hosp, Sch Med, Nanjing 210009, Jiangsu, Peoples R China
关键词
stem cell tracking; superparamagnetic iron oxide; DiD; cardiac function; myocardial infarction; BONE-MARROW; INTRACORONARY INJECTION; PROGENITOR CELLS; HEART-DISEASE; RAT-HEART; THERAPY; CARDIOMYOCYTES; DELIVERY; MODEL;
D O I
10.2147/IJN.S17611
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: Results for implantation efficiency and effective improvement of cardiac function in the field of mesenchymal stem cells (MSCs) are controversial. To attempt to clarify this debate, we utilized magnetic resonance imaging (MRI) and near-infrared optical imaging (OI) to explore the effects of different delivery modes of mesenchymal stem cells on cell retention time and cardiac function after myocardial infarction (MI). Methods: Rat MSCs were labeled with superparamagnetic iron oxide nanoparticles and 1, 1'-dioctadecyl-3,3,3', 3'-tetramethylindodicarbocyanine, 4-chlorobenzenesulfonate salt (DiD) for noninvasive cell tracking in a rat MI model. Rats underwent coronary artery ligation and were randomized into three experimental groups: intravenous (IV), intramyocardial (IM), and a control group. The first two groups referred to the route of delivery of the transplanted dual-labeled MSCs; whereas the control group was given an IV injection of serum-free medium one day post-MI. Cellular engraftment was determined 1 day and 7 days post cell delivery by measuring the iron and optical signals in explanted organs. Prussian blue staining and fluorescent microscopy were performed on histological sections for iron and DiD, respectively. Cardiac function was measured by echocardiography on day 7. Results: The cardiac function of the IM group increased significantly compared to the IV and control groups at day 7. In the IM group, labeled cells were visualized in the infracted heart by serial MRI, and the intensity by OI was significantly higher on day 1. In the IV group, the heart signals were significantly attenuated by dual-modal tracking at two time points, but the lung signals in OI were significantly stronger than the IM group at both time points. Conclusion: IM injection of MSCs increased cell engraftment within infarcted hearts and improved cardiac function after MI. However, IV infusion has a low efficacy due to the cell trapping in the lung. Therefore, direct injection may provide an advantage over IV, with regard to retention of stem cells and protection of cardiac function.
引用
收藏
页码:815 / 823
页数:9
相关论文
共 33 条
[1]   Assessment of the tissue distribution of transplanted human endothelial progenitor cells by radioactive labeling [J].
Aicher, A ;
Brenner, W ;
Zuhayra, M ;
Badorff, C ;
Massoudi, S ;
Assmus, B ;
Eckey, T ;
Henze, E ;
Zeiher, AM ;
Dimmeler, S .
CIRCULATION, 2003, 107 (16) :2134-2139
[2]   Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium - Feasibility, cell migration, and body distribution [J].
Barbash, IM ;
Chouraqui, P ;
Baron, J ;
Feinberg, MS ;
Etzion, S ;
Tessone, A ;
Miller, L ;
Guetta, E ;
Zipori, D ;
Kedes, LH ;
Kloner, RA ;
Leor, J .
CIRCULATION, 2003, 108 (07) :863-868
[3]   Transplantation of autologous fresh bone marrow into infarcted myocardium:: A word of caution [J].
Bel, A ;
Messas, E ;
Agbulut, O ;
Richard, P ;
Samuel, JL ;
Bruneval, P ;
Hagège, AA ;
Menasché, P .
CIRCULATION, 2003, 108 (10) :247-252
[4]   Bone marrow-derived stromal cells home to and remain in the infarcted rat heart but fail to improve function: an in vivo cine-MRI study [J].
Carr, Carolyn A. ;
Stuckey, Daniel J. ;
Tatton, Louise ;
Tyler, Damian J. ;
Hale, Sarah J. M. ;
Sweeney, Dominic ;
Schneider, Juergen E. ;
Martin-Rendon, Enca ;
Radda, George K. ;
Harding, Sian E. ;
Watt, Suzanne M. ;
Clarke, Kieran .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2008, 295 (02) :H533-H542
[5]   Stem cell mechanisms and paracrine effects: Potential in cardiac surgery [J].
Crisostomo, Paul R. ;
Wang, Meijing ;
Markel, Troy A. ;
Lahm, Tim ;
Abarbanell, Aaron M. ;
Herrmann, Jeremy L. ;
Meldrum, Daniel R. .
SHOCK, 2007, 28 (04) :375-383
[6]   Noninvasive tracking of cardiac embryonic stem cells in vivo using magnetic resonance imaging techniques [J].
Ebert, Steven N. ;
Taylor, David G. ;
Nguyen, Ha-Long ;
Kodack, David P. ;
Beyers, Ronald J. ;
Xu, Yaqin ;
Yang, Zequan ;
French, Brent A. .
STEM CELLS, 2007, 25 (11) :2936-2944
[7]   A quantitative, randomized study evaluating three methods of mesenchymal stem cell delivery following myocardial infarction [J].
Freyman, T ;
Polin, G ;
Osman, H ;
Crary, J ;
Lu, MM ;
Cheng, L ;
Palasis, M ;
Wilensky, RL .
EUROPEAN HEART JOURNAL, 2006, 27 (09) :1114-1122
[8]   In vivo tracking in cardiac stem cell-based therapy [J].
Hoshino, Kozo ;
Ly, Hung Q. ;
Frangioni, John V. ;
Hajjar, Roger J. .
PROGRESS IN CARDIOVASCULAR DISEASES, 2007, 49 (06) :414-420
[9]   Mesenchymal stem cells in the infarcted heart [J].
Jain, M ;
Pfister, O ;
Hajjar, RJ ;
Liao, RL .
CORONARY ARTERY DISEASE, 2005, 16 (02) :93-97
[10]   Autologous bone marrow-derived stem-cell transfer in patients with ST-segment elevation myocardial infarction: double-blind, randomised controlled trial [J].
Janssens, S ;
Dubois, C ;
Bogaert, J ;
Theunissen, K ;
Deroose, C ;
Desmet, W ;
Kolantzi, M ;
Herbots, L ;
Sinnaeve, P ;
Dens, J ;
Maertens, J ;
Rademakers, F ;
Dymarkowski, S ;
Gheysens, O ;
Van Cleemput, J ;
Bormans, G ;
Nuyts, J ;
Belmans, A ;
Mortelmans, L ;
Boogaerts, M ;
Van de Werf, F .
LANCET, 2006, 367 (9505) :113-121