Timing of transplantation of autologous bone marrow derived mesenchymal stem cells for treating myocardial infarction

被引:21
作者
Chen YiHuan
Teng XiaoMei
Chen WeiQian
Yang JunJie
Yang ZiYing
Yu YunSheng
Shen ZhenYa [1 ]
机构
[1] Soochow Univ, Dept Cardiovasc Surg, Affiliated Hosp 1, Suzhou 215006, Peoples R China
关键词
bone marrow mesenchymal stem cells (BMSCs); cell transplantation; myocardial infarction; NF-KAPPA-B; PATHWAYS; REPAIR; HEART;
D O I
10.1007/s11427-013-4605-y
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is still unclear whether the timing of intracoronary stem cell therapy affects the therapeutic response in patients with myocardial infarction. The natural course of healing the infarction and the presence of putative homing signals within the damaged myocardium appear to favor cell engraftment during the transendothelial passage in the early days after reperfusion. However, the adverse inflammatory environment, with its high oxidative stress, might be deleterious if cells are administered too early after reperfusion. Here we highlight several aspects of the timing of intracoronary stem cell therapy. Our results showed that transplantation of bone marrow mesenchymal stem cells at 2-4 weeks after myocardial infarction is more favorable for reduction of the scar area, inhibition of left ventricular remodeling, and recovery of heart function. Coronary injection of autologous bone marrow mesenchymal stem cells at 2-4 weeks after acute myocardial infarction is safe and does not increase the incidence of complications.
引用
收藏
页码:195 / 200
页数:6
相关论文
共 18 条
[1]   Reactive oxygen species activate the HIF-1α promoter via a functional NFκB site [J].
Bonello, Steve ;
Zahringer, Christian ;
BelAiba, Rachida S. ;
Djordjevic, Talija ;
Hess, John ;
Michiels, Carine ;
Kietzmann, Thomas ;
Goerlach, Agnes .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (04) :755-761
[2]   Amelioration of angiotensin II-induced cardiac injury by a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor [J].
Dechend, R ;
Fiebeler, A ;
Park, JK ;
Muller, DN ;
Theuer, J ;
Mervaala, E ;
Bieringer, M ;
Gulba, D ;
Dietz, R ;
Luft, FC ;
Haller, H .
CIRCULATION, 2001, 104 (05) :576-581
[3]   Induction and suppression of interferon-inducible protein (IP)-10 in reperfused myocardial infarcts may regulate angiogenesis [J].
Frangogiannis, NG ;
Mendoza, LH ;
Lewallen, M ;
Michael, LH ;
Smith, CW ;
Entman, ML .
FASEB JOURNAL, 2001, 15 (06) :1428-+
[4]   Local implantation of autologous bone marrow cells for therapeutic angiogenesis in patients with ischemic heart disease - Clinical trial and preliminary results [J].
Hamano, K ;
Nishida, M ;
Hirata, K ;
Mikamo, A ;
Li, TS ;
Harada, M ;
Miura, T ;
Matsuzaki, M ;
Esato, K .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 2001, 65 (09) :845-847
[5]   Stimulation of paracrine pathways with growth factors enhances embryonic stem cell engraftment and host-specific differentiation in the heart after ischemic myocardial injury [J].
Kofidis, T ;
de Bruin, JL ;
Yamane, T ;
Tanaka, M ;
Lebl, DR ;
Swijnenburg, RJ ;
Weissman, IL ;
Robbins, RC .
CIRCULATION, 2005, 111 (19) :2486-2493
[6]   Optimal time for cardiomyocyte transplantation to maximize myocardial function after left ventricular injury [J].
Li, RK ;
Mickle, DAG ;
Weisel, RD ;
Rao, VV ;
Jia, ZQ .
ANNALS OF THORACIC SURGERY, 2001, 72 (06) :1957-1963
[7]   Intracoronary bone marrow cell transfer after myocardial infarction - Eighteen months' follow-up data from the randomized, controlled BOOST (BOne marrOw transfer to enhance ST-elevation infarct regeneration) trial [J].
Meyer, GP ;
Wollert, KC ;
Lotz, J ;
Steffens, J ;
Lippolt, P ;
Fichtner, S ;
Hecker, H ;
Schaefer, A ;
Arseniev, L ;
Hertenstein, B ;
Ganser, A ;
Drexler, H .
CIRCULATION, 2006, 113 (10) :1287-1294
[8]   BRAIN NATRIURETIC PEPTIDE AS A NOVEL CARDIAC HORMONE IN HUMANS - EVIDENCE FOR AN EXQUISITE DUAL NATRIURETIC PEPTIDE SYSTEM, ATRIAL-NATRIURETIC-PEPTIDE AND BRAIN NATRIURETIC PEPTIDE [J].
MUKOYAMA, M ;
NAKAO, K ;
HOSODA, K ;
SUGA, S ;
SAITO, Y ;
OGAWA, Y ;
SHIRAKAMI, G ;
JOUGASAKI, M ;
OBATA, K ;
YASUE, H ;
KAMBAYASHI, Y ;
INOUYE, K ;
IMURA, H .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (04) :1402-1412
[9]   Integrating cell-signalling pathways with NF-κB and IKK function [J].
Perkins, Neil D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (01) :49-62
[10]   β-D-glucoside suppresses tumor necrosis factor-induced activation of nuclear transcription factor κB but potentiates apoptosis [J].
Sarkar, A ;
Sreenivasan, Y ;
Ramesh, GT ;
Manna, SK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) :33768-33781