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Volume 134, Issue 3, Pages 565-573 (September 2007)


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Bone marrow–derived mononuclear cell transplantation improves myocardial recovery by enhancing cellular recruitment and differentiation at the infarction site

Jussi Mäkelä, BMa, Kari Ylitalo, MD, PhDb, Siri Lehtonen, PhDa, Sebastian Dahlbacka, MDa, Eija Niemelä, BMa, Kai Kiviluoma, MD, PhDd, Jussi Rimpiläinen, MD, PhDa, Hanna Alaoja, BMa, Timo Paavonen, MD, PhDc, Petri Lehenkari, MD, PhDa, Tatu Juvonen, MD, PhDaCorresponding Author Informationemail address, Vesa Anttila, MD, PhDa

Received 25 February 2007; received in revised form 18 April 2007; accepted 2 May 2007.

Objective

Stem cell therapy in myocardial infarction is under intensive investigation; however, the mechanisms of recovery and the optimal transplantation technique remain controversial. The goal of this controlled and randomized study was to test the hypothesis that locally injected bone marrow–derived mononuclear cells can focus in on the damaged myocardium and improve cardiac function by means of active participation in remodeling.

Methods

Myocardial infarction was introduced through occlusion of the circumflex coronary artery for 90 minutes in 14 piglets (24.0 ± 4.9 kg) that were randomized to a cell-therapy group (n = 7) and a control group (n = 7). At reperfusion, autologous purified prelabeled or unlabeled cells (108 cells/2 mL) or saline were injected into the myocardium. Cardiac function was measured by using echocardiography preoperatively and postoperatively and at 3 weeks, when hearts were collected for histopathologic examination.

Results

The ejection fraction recovered in the cell-therapy group (P = .02) but failed to recover in the control group, and at 3 weeks, it remained at the lower level compared with that in the cell-therapy group (P = .067). The number of living cells in the necrotic area was significantly greater in the cell-therapy group (P < .001). Labeled cells were detected in the infarcted area, and they showed signs of myocyte differentiation. Furthermore, the proportional area of muscle actin-positive cells at the granulation area was higher in the cell-therapy group (P = .035).

Conclusions

Autologous bone marrow–derived mononuclear cells at the infarcted area localize in the myocardium. The exact mechanism of recovery remains to be determined, but our findings may give new information concerning the cellular events that occur during cell therapy–enhanced recovery.

CTSNet classification3

a Department of Surgery, Clinical Research Center, Oulu University Hospital, University of Oulu, Oulu, Finland

b Department of Cardiology, Clinical Research Center, Oulu University Hospital, University of Oulu, Oulu, Finland

c Department of Pathology, Clinical Research Center, Oulu University Hospital, University of Oulu, Oulu, Finland

d Department of Anaesthesiology, Clinical Research Center, Oulu University Hospital, University of Oulu, Oulu, Finland.

Corresponding Author InformationAddress for reprints: Professor Tatu Juvonen, Department of Surgery, Oulu University Hospital, PO Box 21, 90029 Oulu, Finland.

 The study was supported by the Finnish Heart Research Foundation.

 Drs Lehenkari, Juvonen, and Anttila all contributed equally to this study.

PII: S0022-5223(07)00770-2

doi:10.1016/j.jtcvs.2007.05.004


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