ZFAT is essential for endothelial cell assembly and the branch point formation of capillary-like structures in an angiogenesis model

被引:16
|
作者
Yoshida, Yasuhiro [1 ,2 ]
Tsunoda, Toshiyuki [1 ,3 ]
Takashima, Yasuo [1 ,3 ]
Fujimoto, Takahiro [1 ,3 ]
Doi, Keiko [1 ,3 ]
Sasazuki, Takehiko [4 ]
Kuroki, Masahide [3 ]
Iwasaki, Akinori [2 ]
Shirasawa, Senji [1 ,3 ]
机构
[1] Fukuoka Univ, Fac Med, Dept Cell Biol, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Fac Med, Dept Thorac Endocrine & Pediat Surg, Fukuoka 8140180, Japan
[3] Fukuoka Univ, Ctr Adv Mol Med, Fukuoka 8140180, Japan
[4] Kyushu Univ, Fukuoka 8128582, Japan
基金
日本学术振兴会;
关键词
ZFAT; HUVECs; Endothelial cell assembly; Branch point formation; Vascular remodeling; Angiogenesis; IN-VITRO; DISEASE; GENES; VIVO;
D O I
10.2478/s11658-010-0028-y
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
ZFAT, originally identified as a susceptibility gene for autoimmune thyroid disease, encodes a transcriptional regulator with one AT-hook and 18 C2H2-type zinc-finger domains. It is highly conserved among species. Here, we demonstrate that ZFAT is clearly expressed in human umbilical vein endothelial cells (HUVECs). Furthermore, we show that endothelial cell assembly and the branch point formation of capillary-like structures in HUVECs is impaired by the reduction of ZFAT expression through the use of ZFAT-miRNAs, whereas differences in cell proliferation or apoptotic features were not observed after the reduction in ZFAT expression. These results suggest that ZFAT may have critical roles in the capillary-like network formation that is involved in vascular remodeling. Elucidating the ZFAT-mediated transcriptional network will lead to a better understanding of the molecular mechanisms of angiogenesis.
引用
收藏
页码:541 / 550
页数:10
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