RXR agonist enhances the differentiation of cardiomyocytes derived from embryonic stem cells in serum-free conditions

被引:26
作者
Honda, M
Hamazaki, TS [1 ]
Komazaki, S
Kagechika, H
Shudo, K
Asashima, M
机构
[1] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci Biol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Tokyo 113, Japan
[3] Int Med Ctr Japan, Res Inst, Dept Regenerat Med, Tokyo, Japan
[4] Saitama Med Sch, Dept Anat, Moroyama, Saitama, Japan
[5] Tokyo Med & Dent Univ, Grad Sch Biomed Sci, Lab Organ & Med Chem, Tokyo, Japan
[6] ITSUU Lab, Res Fdn, Tokyo, Japan
基金
日本科学技术振兴机构;
关键词
ES cells; cardiomyocytes; RXR agonist; RXR antagonist; PA024; PA452;
D O I
10.1016/j.bbrc.2005.05.202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signaling from the retinoic acid receptors (RARs) and retinoid X receptors (RXRs) is essential for cardiovascular morphogenesis in vivo. RAR and/or RXR signaling can also enhance the in vitro induction of cardiomyocytes from murine embryonic stem (ES) cells in the presence of serum. The present study examined the effect of RXR agonist that was specifically bound to RXRs on the differentiation of mouse ES cells into cardiomyocytes in vitro in the absence of serum. The number of beating embryoid body-like spheres (EBSs) derived from the ES cells increased significantly following treatment with PA024, an RXR agonist. In contrast, when EBSs were treated with PA452, which was specifically bound to RXR and worked as an antagonist, the number of beating EBSs was decreased in a dose-dependent manner. These results suggest that RXR signaling regulates cardiomyocyte numbers during the differentiation of ES cells in vitro and probably in normal development. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1334 / 1340
页数:7
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