MS-818 accelerates mobilization of endothelial progenitor cells and differentiation to endothelial cells

被引:5
作者
Kanemura, M
Abe, M
Ueda, M
Ueki, M
Awaya, A
Sato, Y
机构
[1] Tohoku Univ, Dept Vasc Biol, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Osaka Med Coll, Dept Obstet & Gynecol, Osaka, Japan
[3] Japan Sci & Technol Agcy, Tokyo, Japan
来源
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH | 2004年 / 11卷 / 5-6期
关键词
angiogenesis; embryonic stem cells (ES cells); endothelial progenitor cells (EPCs); MS-818; vasculogenesis;
D O I
10.1080/10623320490904089
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MS-818 that is a synthetic pyrimidine compound and shown to have neurotrophic actions, enhanced basic fibroblast growth factor (bFGF)-induced angiogenesis in vivo. However, the mechanism and whether MS-818 affects endothelial cells (ECs) directly is not known. Here, the authors investigated whether MS-818 alone could induce angiogenesis and tried to clarify the mechanism of neovascularization by MS-818 in terms of angiogenesis and vasculogenesis. The authors show that MS-818 affects ECs directly and induces migration of and tube formation by ECs in vitro (angiogenesis). Furthermore, the authors demonstrate that MS-818 mobilizes endothelial progenitor cells (EPCs) from the bone marrow and potentiates their differentiation to ECs (vasculogenesis). The effect of MS-818 on the endothelial differentiation was further confirmed with an in vitro differentiation system using mouse embryonic stem cells. MS-818 activates the mitogen-activated protein kinase (MAPK) pathway but not the phosphoinositol 3-kinase (PI3K)-Akt pathway in ECs. These results indicate that MS-818, a synthetic compound, promotes both angiogenesis and vasculogenesis.
引用
收藏
页码:221 / 230
页数:10
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