In situ delivery of bone marrow cells and mesenchymal stem cells improves cardiovascular function in hypertensive rats submitted to myocardial infarction

被引:55
作者
Gomes de Macedo Braga, Luisa Maria [1 ,2 ]
Lacchini, Silvia [3 ]
Schaan, Beatriz D'Agord [3 ,4 ]
Rodrigues, Bruno [3 ]
Rosa, Kaleizu [3 ]
De Angelis, Katia [3 ]
Borges, Luciano Figueiredo [3 ]
Irigoyen, Maria Claudia [3 ]
Nardi, Nance Beyer [1 ]
机构
[1] Univ Fed Rio de Janeiro, Dept Genet, BR-91501970 Porto Alegre, RS, Brazil
[2] State Fdn Prod & Res Hlth Rio Grande Sul, Porto Alegre, RS, Brazil
[3] Univ Sao Paulo, Inst Heart, Hypertens Unit, Sao Paulo, Brazil
[4] Cardiol Fdn, Cardiol Inst, Porto Alegre, RS, Brazil
关键词
bone marrow cells; mesenchymal stem cells; spontaneously hypertensive rats; hypertension; in situ delivery;
D O I
10.1007/s11373-008-9237-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
This work aimed to evaluate cardiac morphology/function and histological changes induced by bone marrow cells (BMCs) and cultured mesenchymal stem cells (MSCs) injected at the myocardium of spontaneously hypertensive rats (SHR) submitted to surgical coronary occlusion. Female syngeneic adult SHR, submitted (MI) or not (C) to coronary occlusion, were treated 24 h later with in situ injections of normal medium (NM), or with MSCs (MSC) or BMCs (BM) from male rats. The animals were evaluated after 1 and 30 days by echocardiography, histology of heart sections and PCR for the Y chromosome. Improved ejection fraction and reduced left ventricle infarcted area were observed in MSC rats as compared to the other experimental groups. Treated groups had significantly reduced lesion tissue score, increased capillary density and normal (not-atrophied) myocytes, as compared to NM and C groups. The survival rate was higher in C, NM and MSC groups as compared to MI and BM groups. In situ injection of both MSCs and BMCs resulted in improved cardiac morphology, in a more physiological model of myocardial infarction represented by surgical coronary occlusion of spontaneously hypertensive rats. Only treatment with MSCs, however, ameliorated left ventricle dysfunction, suggesting a positive role of these cells in heart remodeling in infarcted hypertensive subjects.
引用
收藏
页码:365 / 374
页数:10
相关论文
共 34 条
[1]
Amado LC, 2005, P NATL ACAD SCI USA, V102, P11474, DOI 10.1073/pnas.0504388102
[2]
Skeletal muscle cells expressing VEGF induce capillary formation and reduce cardiac injury in rats [J].
Becker, Claudia ;
Lacchini, Silvia ;
Muotri, Alysson Renato ;
Justo da Silva, Gustavo Jose ;
Castelli, Jussara Bianchi ;
Vassallo, Paula F. ;
Martins Menck, Carlos Frederico ;
Krieger, Jose Eduardo .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2006, 113 (03) :348-354
[3]
Beyer Nardi N, 2006, HANDB EXP PHARM, V174, P249
[4]
BOOMSMA RA, 2006, INT J CARDIOL
[5]
BRAGA LMG, 2007, CLIN EXP PHARM PHYSL, V35
[6]
Mesenchymal stem cells reside in virtually all post-natal organs and tissues [J].
da Silva Meirelles, Lindolfo ;
Chagastelles, Pedro Cesar ;
Nardi, Nance Beyer .
JOURNAL OF CELL SCIENCE, 2006, 119 (11) :2204-2213
[7]
Mesenchymal progenitor cells differentiate into an endothelial phenotype, enhance vascular density, and improve heart function in a rat cellular cardiomyoplasty model [J].
Davani, S ;
Marandin, A ;
Mersin, N ;
Royer, B ;
Kantelip, B ;
Hervé, P ;
Etievent, JP ;
Kantelip, JP .
CIRCULATION, 2003, 108 (10) :253-258
[8]
Nonstimulated cardiomyoplasty improves hemodynamics in myocardial-infarcted rats [J].
De Angelis, K ;
Leirner, AA ;
Irigoyen, MC ;
Cestari, IA .
ARTIFICIAL ORGANS, 2001, 25 (11) :939-943
[9]
Rat models of hypertension, cardiac hypertrophy and failure [J].
Doggrell, SA ;
Brown, L .
CARDIOVASCULAR RESEARCH, 1998, 39 (01) :89-105
[10]
Direct intramyocardial but not intracoronary injection of bone marrow cells induces ventricular arrhythmias in a rat chronic ischemic heart failure model [J].
Fukushima, Satsuki ;
Varela-Carver, Anabel ;
Coppen, Steven R. ;
Yamahara, Kenichi ;
Felkin, Leanne E. ;
Lee, Joon ;
Barton, Paul J. R. ;
Terracciano, Cesare M. N. ;
Yacoub, Magdi H. ;
Suzuki, Ken .
CIRCULATION, 2007, 115 (17) :2254-2261