Skip Navigation


Cardiovascular Research Advance Access originally published online on September 27, 2007
Cardiovascular Research 2008 77(1):143-150; doi:10.1093/cvr/cvm027
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Data
Right arrow All Versions of this Article:
77/1/143    most recent
cvm027v2
cvm027v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Lutz, M.
Right arrow Articles by Frey, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lutz, M.
Right arrow Articles by Frey, N.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2007. For permissions please email: journals.permissions@oxfordjournals.org

Local injection of stem cell factor (SCF) improves myocardial homing of systemically delivered c-kit + bone marrow-derived stem cells

Matthias Lutz1,{dagger}, Mark Rosenberg1,{dagger}, Fabian Kiessling2, Volker Eckstein3, Thomas Heger1, Jutta Krebs1, Anthony D. Ho3, Hugo A. Katus1 and Norbert Frey1,*

1 Department of Cardiology, Internal Medicine III, University of Heidelberg, INF 410, D-69120 Heidelberg, Germany
2 Department of Medical Physics in Radiology, German Cancer Research Center, INF 280, D-69120 Heidelberg, Germany
3 Department of Hematology, Internal Medicine V, University of Heidelberg, INF 410, D-69120 Heidelberg, Germany

* Corresponding author. Tel: +49 6221 561505; fax: +49 6221 568647. E-mail address: norbert.frey{at}med.uni-heidelberg.de, freynorbert{at}hotmail.com

Aims: Recent studies have shown that stem cell therapy may alleviate the detrimental effects of myocardial infarction. Yet, most of these reports observed only modest effects on cardiac function, suggesting that there still is need for improvement before widespread clinical use. One potential approach would be to increase migration of stem cells to the heart. We therefore tested whether local administration of stem cell factor (SCF) improves myocardial homing of intravenously infused lin-/c-kit+ stem cells after myocardial infarction.

Methods and results: Myocardial infarction was induced in mice via ligation of the left anterior descending artery and 2.5 µg of SCF were injected into the peri-infarct zone. Sham-operated mice and animals with intramyocardial injection of phosphate-buffered saline (PBS) served as controls. Twenty-four hours after myocardial infarction, lin-/c-kit+ stem cells were separated from murine bone marrow by magnetic cell sorting, labelled with the green fluorescent cell tracker CFDA or 111Indium, and subsequently 750 000 labelled cells were systemically infused via the tail vein. Another 24 or 72 h later, respectively (i.e. 48 and 96 h after myocardial infarction), hearts were removed and analysed for myocardial homing of stem cells. Green fluorescent stem cells were exclusively detected in the peri-infarct zone of animals having prior SCF treatment. Radioactive measurements revealed that an intramyocardial SCF injection significantly amplified myocardial homing of lin-/c-kit+ stem cells compared to animals with PBS injections (3.58 ± 0.53 vs. 2.28 ± 0.23 cpm/mg/106cpm, +60%, P < 0.05) and sham-operated mice without myocardial infarction (3.58 ± 0.53 vs. 1.95 ± 0.22 cpm/mg/106cpm, +85%, P < 0.01). Similar results were obtained 72 h after stem cell injection.

Conclusion: We demonstrate that intramyocardial administration of SCF sustainably directs more lin-/c-kit+ stem cells to the heart. Future studies will have to show whether higher levels of myocardial SCF (i.e. by virus-mediated gene transfer) can further improve homing of systemically delivered c-kit+ stem cells and thus favourably influence cardiac remodelling following myocardial infarction.

KEYWORDS Stem cells; Homing; Myocardial infarction; Stem Cell Factor (SCF)


Time for primary review 18 days

{dagger} These authors contributed equally to this study


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
CirculationHome page
F.-L. Xiang, X. Lu, L. Hammoud, P. Zhu, P. Chidiac, J. Robbins, and Q. Feng
Cardiomyocyte-Specific Overexpression of Human Stem Cell Factor Improves Cardiac Function and Survival After Myocardial Infarction in Mice
Circulation, September 22, 2009; 120(12): 1065 - 1074.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.