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Tissue-Specific Stem Cells
Article first published online: 22 OCT 2012
Copyright © 2012 AlphaMed Press
Volume 30, Issue 11, pages 2512–2522, November 2012
How to Cite
Cottage, C. T., Neidig, L., Sundararaman, B., Din, S., Joyo, A. Y., Bailey, B., Gude, N., Hariharan, N. and Sussman, M. A. (2012), Increased Mitotic Rate Coincident with Transient Telomere Lengthening Resulting from Pim-1 Overexpression in Cardiac Progenitor Cells. STEM CELLS, 30: 2512–2522. doi: 10.1002/stem.1211
Author contributions: C.T.C.: conception and design, collection and/or assembly of data, data analysis and interpretation, and manuscript writing, L.N., B.S., S.D., A.J., B.B., N.G., and N.H.: collection and/or assembly of data, M.S.: conception and design, financial support, manuscript writing, and final approval of manuscript.
Disclosure of potential conflicts of interest is found at the end of this article.
First published online in STEM CELLSEXPRESS August 22, 2012.
- Issue published online: 22 OCT 2012
- Article first published online: 22 OCT 2012
- Accepted manuscript online: 22 AUG 2012 10:40AM EST
- Manuscript Accepted: 23 JUL 2012
- Manuscript Received: 7 JUN 2012
- National Heart, Lung, and Blood Institute. Grant Numbers: R21-HL102714, R01-HL067245, R37-HL091102, P01-HL085577, RC1-HL100891, R21-HL102613, R21 HL104544, R01 HL105759
- Rees-Stealy Research Foundation
- San Diego ARCS Foundation
- American Heart Association Pre-doctoral Fellowship. Grant Number: 10PRE3060046
- Inamori Foundation Fellowship
- Cardiac progenitor cell;
Cardiac regeneration following myocardial infarction rests with the potential of c-kit+ cardiac progenitor cells (CPCs) to repopulate damaged myocardium. The ability of CPCs to reconstitute the heart is restricted by patient age and disease progression. Increasing CPC proliferation, telomere length, and survival will improve the ability of autologous CPCs to be successful in myocardial regeneration. Prior studies have demonstrated enhancement of myocardial regeneration by engineering CPCs to express Pim-1 kinase, but cellular and molecular mechanisms for Pim-1-mediated effects on CPCs remain obscure. We find CPCs rapidly expand following overexpression of cardioprotective kinase Pim-1 (CPCeP), however, increases in mitotic rate are short-lived as late passage CPCePs proliferate similar to control CPCs. Telomere elongation consistent with a young phenotype is observed following Pim-1 modification of CPCeP; in addition, telomere elongation coincides with increased telomerase expression and activity. Interestingly, telomere length and telomerase activity normalize after several rounds of passaging, consistent with the ability of Pim-1 to transiently increase mitosis without resultant oncogenic transformation. Accelerating mitosis in CPCeP without immortalization represents a novel strategy to expand the CPC population in order to improve their therapeutic efficacy. STEM CELLS2012;30:2512–2522