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European Journal of Heart Failure 2008 10(2):119-124; doi:10.1016/j.ejheart.2007.11.009
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© 2008 European Society of Cardiology

Impact of different bone marrow cell preparations on left ventricular remodelling after experimental myocardial infarction

Stefan Frantza, Duttu Vallabhapurapub, Jochen Tillmannsa, Nikos Brousosb, Helga Wagnera, Kristina Heniga, Georg Ertla, Albrecht M. Müllerb,1 and Johann Bauersachsa,*,1

a Medizinische Klinik und Poliklinik I, Universitätsklinikum, Julius-Maximilians-Universität Würzburg Germany
b Institut für Medizinische Strahlenkunde und Zellforschung, Julius-Maximilians-Universität Würzburg Germany

* Corresponding author. Medizinische Klinik und Poliklinik I, Universitätsklinikum der Julius-Maximilians-Universität Würzburg, Josef Schneider-Str. 2, 97080 Würzburg, Germany. Tel.: +49 931 201 0; fax: +49 931 201 36135. E-mail address: bauersachs_j{at}medizin.uni-wuerzburg.de (J. Bauersachs).


   Abstract

Objective: Bone marrow (BM)-derived haematopoietic stem cells have been proposed as a potential cell source to functionally engraft the myocardium and to improve cardiac function after myocardial infarction (MI). However, experimental and clinical data are inconsistent. Since the specific characteristics of different BM cell subsets could influence their therapeutic potential we determined the effect of different BM cell populations on left ventricular remodelling after MI.

Methods and results: MI was induced in female mice by coronary artery ligation. Surviving mice were randomised to receive either: total BM, mature Lin+ or primitive Lin cells from male mice, or saline, via intracardiac injection. Injected cells were detected in the infarct and border zone by PCR for Y-chromosomal sequences. Serial transthoracic echocardiography was performed 1, 21, and 42 days after MI. Over a period of 6 weeks, mortality was not different between the groups. After MI, animals exhibited left ventricular dilatation, as expected. Left ventricular remodelling was not influenced by Lin+ or Lin BM cells but was partially improved by unfractionated BM cell injection. Paracrine secretion of cytokines (e.g. IL-6, GM-CSF) was differentially regulated in supernatants of cultured BM cells.

Summary: Treatment with unfractionated BM cells, but not Lin+, or Lin cells partially improved cardiac remodelling and function after MI. This may be mediated by paracrine effects.

Key Words: Myocardial infarction • Remodelling • BM cell injection • Cytokine

Received June 29, 2007; Revised October 25, 2007; Accepted November 12, 2007


1 Both authors contributed equally to the work.


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