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The Rat Myosin Light Chain Promoter-Driven DsRed Reporter System Allows Specific Monitoring of Bone Marrow Mesenchymal Stem Cell-Derived CardiomyocytesThe Rat Myosin Light Chain Promoter-Driven DsRed Reporter System Allows Specific Monitoring of Bone Marrow Mesenchymal Stem Cell-Derived Cardiomyocytes

Other Titles
The Rat Myosin Light Chain Promoter-Driven DsRed Reporter System Allows Specific Monitoring of Bone Marrow Mesenchymal Stem Cell-Derived Cardiomyocytes
Authors
최승철임도선
Issue Date
2008
Publisher
사단법인 한국동물생명공학회
Keywords
Cardiomyogenic differentiation; DsRed; Promoter; Mesenchymal stem cells; Reporter gene; Cardiomyogenic differentiation; DsRed; Promoter; Mesenchymal stem cells; Reporter gene
Citation
Reproductive & Developmental biology, v.32, no.1, pp.21 - 25
Indexed
KCI
Journal Title
Reproductive & Developmental biology
Volume
32
Number
1
Start Page
21
End Page
25
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/124734
ISSN
1738-2432
Abstract
Bone marrow mesenchymal stem cells (BMMSCs) have the capacity for self-renewal and differentiation into a variety of cell types. They represent an attractive source of cells for gene and cell therapy. The purpose of this study is to direct the specific expression of the DsRed reporter gene in Sca-1+ BMMSCs differentiated into a cardiomyogenic lineage. We constructed the prMLC-2v-DsRed vector expressing DsRed under the control of the 309 bp fragment of the rat MLC-2v 5'-flanking region. The specific expression of the DsRed reporter gene under the transcriptional control of the 309 bp fragment of the rat MLC-2v promoter was tested in 5-azacytidine treated-Sca-1+ BMMSCs over 2 weeks after the prMLC-2v-DsRed transfection. The prMLC-2v-DsRed was specifically expressed in the Sca-1+ BMMSCs with cardiomyogenic lineage differentiation, and it demonstrates that the 309 bp sequences of the rat MLC-2v 5'-flanking region is sufficient to confer cardiac specific expression on a DsRed reporter gene. The cardiac-specific promoter-driven reporter vector provides an important tool for the study of stem cell differentiation and cell replacement therapy in ischemic cardiomyopathy.
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