...
首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The microRNA-30 family targets DLL4 to modulate endothelial cell behavior during angiogenesis
【24h】

The microRNA-30 family targets DLL4 to modulate endothelial cell behavior during angiogenesis

机译:microRNA-30家族靶向DLL4在血管生成过程中调节内皮细胞行为

获取原文
获取原文并翻译 | 示例

摘要

Delta-like 4 (DLL4), a membrane-bound ligand belonging to the Notch signaling family, plays a fundamental role in vascular development and angiogenesis. We identified a conserved microRNA family, miR-30, which targets DLL4. Overexpression of miR-30b in endothelial cells led to increased vessel number and length in an in vitro model of sprouting angiogenesis. Microinjection of miR-30 mimics into zebrafish embryos resulted in suppression of dll4 and subsequent excessive sprouting of intersegmental vessels and reduction in dorsal aorta diameter. Use of a target protector against the miR-30 site within the dll4 3′UTR up-regulated dll4 and synergized with Vegfa signaling knockdown to inhibit angiogenesis. Furthermore, restoration of miR-30b or miR- 30c expression during Kaposi sarcoma herpesvirus (KSHV) infection attenuated viral induction of DLL4. Together these results demonstrate that the highly conserved molecular targeting of DLL4 by the miR-30 family regulates angiogenesis.
机译:Delta-like 4(DLL4)是属于Notch信号家族的膜结合配体,在血管发育和血管生成中起着重要作用。我们确定了一个保守的microRNA家族,miR-30,针对DLL4。在萌发性血管生成的体外模型中,内皮细胞中miR-30b的过表达导致血管数量和长度的增加。将miR-30模拟物显微注射到斑马鱼胚胎中导致dll4的抑制和随后的节间血管的过度发芽以及背主动脉直径的减小。使用针对dll4 3'UTR上调dll4中的miR-30位点的靶保护子,并与Vegfa信号敲低协同增效,以抑制血管生成。此外,在卡波西氏肉瘤疱疹病毒(KSHV)感染期间恢复miR-30b或miR-30c的表达减弱了DLL4的病毒诱导。这些结果共同证明,miR-30家族对DLL4高度保守的分子靶向作用可调节血管生成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号