Bone marrow-derived side population cells are capable of functional cardiomyogenic differentiation
- Authors
- Yoon, Jihyun; Choi, Seung Cheol; Park, Chi Yeon; Choi, Ji-Hyun; Kim, Yang In; Shim, Wan Joo; Lim, Do Sun
- Issue Date
- Apr-2008
- Publisher
- 한국분자세포생물학회
- Keywords
- Bone Marrow; Cardiomyogenic Differentiation; Side Population Cells
- Citation
- Molecules and Cells, v.25, no.2, pp 216 - 223
- Pages
- 8
- Indexed
- SCOPUS
KCI
- Journal Title
- Molecules and Cells
- Volume
- 25
- Number
- 2
- Start Page
- 216
- End Page
- 223
- URI
- https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62959
- ISSN
- 1016-8478
0219-1032
- Abstract
- It has been reported that bone marrow (BM)-side population (SP) cells, with hematopoietic stem cell activity, can transdifferentiate into cardiomyocytes and contribute to myocardial repair. However, this has been questioned by recent studies showing that hematopoietic stem cells (HSCs) adopt a hematopoietic cell lineage in the ischemic myocardium. The present study was designed to investigate whether BM-SP cells can in fact transdifferentiate into functional cardiomyocytes. Phenotypically, BM-SP cells were 19.59% +/- 9.00 CD14(+), 8.22% +/- 2.72 CD34(+), 92.93% +/- 2.68 CD44(+), 91.86% +/- 4.07 CD45(+), 28.48% +/- 2.24 c-kit(+), 71.09% +/- 3.67 Sca-1(+). Expression of endothelial cell markers (CD31, Flk-1, Tie-2 and VEGF-A) was higher in BM-SP cells than whole BM cells. After five days of co-culture with neonatal cardiomyocytes, 7.2% +/- 1.2 of the BM-SP cells expressed sarcomeric alpha-actinin as measured by flow cytometry. Moreover, BM-SP cells co-cultured on neonatal cardiomyocytes fixed to inhibit cell fusion also expressed sarcomeric alpha-actinin. The co-cultured BM-SP cells showed neonatal cardiomyocyte-like action potentials of relatively long duration and shallow resting membrane potential. They generated calcium transients with amplitude and similar to those of neonatal cardiomyocytes. results show that BM-SP cells are capable of cardiomyogenic differentiation when co-cultured with neonatal cardiomyocytes.
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