Significant improvement of heart function by cotransplantation of human mesenchymal stem cells and fetal cardiomyocytes in postinfarcted pigs

被引:130
作者
Min, JY
Sullivan, MF
Yang, Y
Zhang, JP
Converso, KL
Morgan, JP
Xiao, YF
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med,Thorndike Lab, Dept Med,Cardiovasc Div, Boston, MA 02215 USA
[2] Charles A Dana Res Inst, Stem Cell Res Lab, Boston, MA 02215 USA
关键词
D O I
10.1016/S0003-4975(02)03952-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Viable cardiomyocytes after myocardial infarction (MI) are unable to repair the necrotic myocardium due to their limited capability of regeneration. The present study investigated whether intramyocardial transplantation of human mesenchymal stem cells (hMSCs) or cotransplantation of hMSCs plus human fetal cardiomyocytes (hFCs; 1:1) reconstituted impaired myocardium and improved cardiac function in MI pigs. Methods and Results. Cultured hMSCs were transfected with green fluorescent protein (GFP). Six weeks after MI induction and cell transplantation, cardiac function was significantly improved in MI pigs transplanted with hMSCs alone. However, the improvement was even markedly greater in MI pigs cotransplanted with hMSCs plus hFCs. Histological examination demonstrated that transplantation of hMSCs alone or hMSCs plus hFCs formed GFP-positive engrafts in infarcted myocardium. In addition, immunostaining for cardiac a-myosin heavy chain and troponin I showed positive stains in infarcted regions transplanted with hMSCs alone or hMSCs plus hFCs. Conclusions. Our data demonstrate that transplantation of hMSCs alone improved cardiac function in MI pigs with a markedly greater improvement from cotransplantation of hMSCs plus hFCs. This improvement might result from myocardial regeneration and angiogenesis in injured hearts by engrafted cells. (C) 2002 by The Society of Thoracic Surgeons.
引用
收藏
页码:1568 / 1575
页数:8
相关论文
共 32 条
[1]   Evidence that human cardiac myocytes divide after myocardial infarction (Publication with Expression of Concern. See vol. 379, pg. 1870, 2018) [J].
Beltrami, AP ;
Urbanek, K ;
Kajstura, J ;
Yan, SM ;
Finato, N ;
Bussani, R ;
Nadal-Ginard, B ;
Silvestri, F ;
Leri, A ;
Beltrami, CA ;
Anversa, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (23) :1750-1757
[2]  
CHIU RCJ, 1995, ANN THORAC SURG, V60, P12
[3]   DIFFERENTIATION OF MUSCLE, FAT, CARTILAGE, AND BONE FROM PROGENITOR CELLS PRESENT IN A BONE-DERIVED CLONAL CELL-POPULATION - EFFECT OF DEXAMETHASONE [J].
GRIGORIADIS, AE ;
HEERSCHE, JNM ;
AUBIN, JE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (06) :2139-2151
[4]   BASIC FIBROBLAST GROWTH-FACTOR IMPROVES MYOCARDIAL-FUNCTION IN CHRONICALLY ISCHEMIC PORCINE HEARTS [J].
HARADA, K ;
GROSSMAN, W ;
FRIEDMAN, M ;
EDELMAN, ER ;
PRASAD, PV ;
KEIGHLEY, CS ;
MANNING, WJ ;
SELLKE, FW ;
SIMONS, M .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) :623-630
[5]   BLOOD-FLOW MEASUREMENTS WITH RADIONUCLIDE-LABELED PARTICLES [J].
HEYMANN, MA ;
PAYNE, BD ;
HOFFMAN, JIE ;
RUDOLPH, AM .
PROGRESS IN CARDIOVASCULAR DISEASES, 1977, 20 (01) :55-79
[6]   LONG-TERM SURVIVAL OF AT-1 CARDIOMYOCYTE GRAFTS IN SYNGENEIC MYOCARDIUM [J].
KOH, GY ;
SOONPAA, MH ;
KLUG, MG ;
FIELD, LJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :H1727-H1733
[7]  
Le Blanc Katarina, 2002, Lakartidningen, V99, P1318
[8]  
Leor J, 1996, CIRCULATION, V94, P332
[9]  
Li RK, 1996, ANN THORAC SURG, V62, P654
[10]   Human pediatric and adult ventricular cardiomyocytes in culture, assessment of phenotypic changes with passaging [J].
Li, RK ;
Mickle, DAG ;
Weisel, RD ;
Carson, S ;
Omar, SA ;
Tumiati, LC ;
Wilson, GJ ;
Williams, WG .
CARDIOVASCULAR RESEARCH, 1996, 32 (02) :362-373