Coexpression of platelet-derived growth factor receptor alpha and fetal liver kinase 1 enhances cardiogenic potential in embryonic stem cell differentiation in vitro

被引:29
作者
Hirata, Hirokazu
Kawamata, Shin
Murakami, Yoshinobu
Inoue, Kayoko
Nagahashi, Ayako
Tosaka, Mako
Yoshimura, Naoko
Miyamoto, Yoshiaki
Iwasaki, Hiroto
Asahara, Takayuki
Sawa, Yoshiki
机构
[1] Fdn Biomed Res & Innovat, Dept Tissue Engn & Cell Therapy, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Kyoto Univ, Inst Frontier Med Sci, Sakyo Ku, Kyoto 6068507, Japan
[3] RIKEN, Ctr Dev Biol, Chuo Ku, Kobe, Hyogo 6500047, Japan
[4] Osaka Univ, Grad Sch Med, Div Cardiovasc Surg, Dept Surg, Suita, Osaka 5650871, Japan
关键词
platelet-derived growth factor receptor alpha (PDGFR alpha); embryonic stem cell; cardiac differentiation; cardiac precursor; MOUSE EMBRYOGENESIS; LIMITING DILUTION; PROGENITOR CELLS; EXPRESSION; KINASE; VASCULOGENESIS; LINEAGE; FLK-1; GUIDANCE; ASSAYS;
D O I
10.1263/jbb.103.412
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nascent mesodermal cells derived from EB5 embryonic stem (ES) cells were sorted in terms of cardiogenic potential on the basis of their expression levels of platelet-derived growth factor receptor alpha (PDGFR alpha) and fetal liver kinase 1 (Flk-1). The sorted cells were cocultured with OP9 stromal cells to induce terminal differentiation into contractile cardiac colonies. A significant number of cardiac colonies were found in the Flk-1+/PDGFR alpha+ fraction. The enrichment double-positive fraction produced approximately fivefold more cardiac colonies than the Flk-1+/PDGFR alpha-fraction and 10-fold more than the Flk-1-/PDGFR alpha+ fraction. To investigate the involvement of these markers in embryonic cardiogenesis, the cells that disseminated from the E7.5-7.75 embryos were fractionated and seeded on OP9 cells. The cardiogenic potential was markedly enhanced in the Flk-1+/PDGFRa+ fraction. These results suggest that some of the precursor cells coexpressing these markers are selectively involved in cardiogenic events, and that the identification of ES-cell-derived precursors with these markers will contribute to the effective production of cardiomyocytes for cell therapies.
引用
收藏
页码:412 / 419
页数:8
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