Endoventricular porcine autologous myoblast transplantation can be successfully achieved with minor mechanical cell damage

被引:31
作者
Chazaud, W
Hittinger, L
Sonnet, C
Champagne, S
Le Corvoisier, P
Benhaiem-Sigaux, N
Unterseeh, T
Su, JB
Merlet, P
Rahmouni, A
Garot, J
Gherardi, R
Teiger, E
机构
[1] Hop Henri Mondor, Serv Explorat Fonct, F-94010 Creteil, France
[2] Fac Med, INSERM U492, Creteil, France
[3] Hop Henri Mondor, Serv Radiol & Imagerie Med, F-94010 Creteil, France
[4] Hop Henri Mondor, Nucl Med Serv, F-94010 Creteil, France
[5] Hop Henri Mondor, Serv Histoembryol Cytogenet, F-94010 Creteil, France
[6] Hop Henri Mondor, Ctr Rech Chirurg, F-94010 Creteil, France
[7] Fac Med, INSERM U400, F-94010 Creteil, France
[8] Hop Henri Mondor, Federat Cardiol, F-94010 Creteil, France
[9] Hop Henri Mondor, INSERM E0011, F-94010 Creteil, France
关键词
heart failure; infarction; myocytes; stem cells; transplantation;
D O I
10.1016/S0008-6363(02)00834-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Transplantation of skeletal myogenic precursor cells (mpc) into the myocardium using a non-surgical procedure. Methods: Closed-chest mpc transplantation Was assessed in pigs using the NOGA-Biosense(R) device allowing both electromechanical mapping of the left ventricle (LV), and guided mpc injections through endocardium. Results: We successively established that: (1) adequate preimplantation handling of mpc can be achieved when mpc are kept in 0.1% serum albumin-containing medium until implantation; (2) mpc are neither retained nor destroyed in the catheter or the needle and their passage does not affect their survival, growth and differentiation; (3) large numbers of autologous mpc can be actually transplanted in the LV myocardium by transendocardial route, as assessed by post-mortem examination of pigs injected with iron-loaded mpc; (4) cell injection into the myocardium does not induce conspicuous cell mortality since more than 80% of mpc recovered from LV tissue are alive 15 min after injection; (5) mpc injections can be guided into circumscribed LV targets such as infarcted areas, as assessed by comparison of map injection sites with location of iron-loaded mpc at post-mortem examination of LV myocardium. Conclusion: This new approach may pave the way for a large spectrum of cell therapies targeting myocardial diseases. (C) 2003 European Society of Cardiology. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:444 / 450
页数:7
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