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Intracardiac injection of matrigel induces stem cell recruitment and improves cardiac functions in a rat myocardial infarction model
Authors:Lailiang Ou  Wenzhong Li  Yue Zhang  Weiwei Wang  Jun Liu  Heiko Sorg  Dario Furlani  Ralf Gäbel  Peter Mark  Christian Klopsch  Liang Wang  Karola Lützow  Andreas Lendlein  Klaus Wagner  Doris Klee  Andreas Liebold  Ren‐Ke Li  Deling Kong  Gustav Steinhoff  Nan Ma
Institution:1. Reference‐ and Translation Center for Cardiac Stem Cell Therapy (RTC), Department of Cardiac Surgery, University of Rostock, Rostock, Germany;2. Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Science, Nankai University, Tianjin, China;3. Institute of Polymer Research, GKSS Research Center, Geesthacht, Germany;4. Department of Anesthesia, Klinikum Südstadt Rostock, Rostock, Germany;5. Institute of Technical and Macromolecular Chemistry Aachen, Aachen, Germany;6. Division of Cardiovasculary Surgery, Toronto General Hospital and the University of Toronto, Toronto, Canada
Abstract:Matrigel promotes angiogenesis in the myocardium from ischemic injury and prevents remodelling of the left ventricle. We assessed the therapeutic efficacy of intracardiac matrigel injection and matrigel‐mediated stem cell homing in a rat myocardial infarction (MI) model. Following MI, matrigel (250 μl) or phosphate‐buffered solution (PBS) was delivered by intracardiac injection. Compared to the MI control group (MI‐PBS), matrigel significantly improved left ventricular function (n= 11, P < 0.05) assessed by pressure–volume loops after 4 weeks. There is no significant difference in infarct size between MI‐matrigel (MI‐M; 21.48 ± 1.49%, n= 10) and MI‐PBS hearts (20.98 ± 1.25%, n= 10). The infarct wall thickness of left ventricle is significantly higher (P < 0.01) in MI‐M (0.72 ± 0.02 mm, n= 10) compared with MI‐PBS (0.62 ± 0.02 mm, n= 10). MI‐M hearts exhibited higher capillary density (border 130.8 ± 4.7 versus 115.4 ± 6.0, P < 0.05; vessels per high‐power field HPF; 400×], n= 6) than MI‐PBS hearts. c‐Kit+ stem cells (38.3 ± 5.3 versus 25.7 ± 1.5 c‐Kit+ cells per HPF 630×], n= 5, P < 0.05) and CD34+ cells (13.0 ± 1.51 versus 5.6 ± 0.68 CD34+ cells per HPF 630×], n= 5, P < 0.01) were significantly more numerous in MI‐M than in MI‐PBS in the infarcted hearts (n= 5, P < 0.05). Intracardiac matrigel injection restores myocardial functions following MI, which may attribute to the improved recruitment of CD34+ and c‐Kit+ stem cells.
Keywords:cardiac regeneration  ischemia  matrigel  stem and progenitor cells
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