Morita Rimpei, Suzuki Mayu, Kasahara Hidenori, Shimizu Nana, Shichita Takashi, Sekiya Takashi, Kimura Akihiro, Sasaki Ken-ichiro, Yasukawa Hideo, Yoshimura Akihiko
Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan; Core Research for Evolutional Science and Technology Program, Japan Science and Technology Agency, Tokyo 102-0076, Japan;
Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo 160-8582, Japan; Core Research for Evolutional Science and Technology Program, Japan Science and Technology Agency, Tokyo 102-0076, Japan; PRESTO (Precursory Research for Embryonic Science and Technology), Chiyoda-ku, Tokyo 102-0075, Japan; and.
Proc Natl Acad Sci U S A. 2015 Jan 6;112(1):160-5. doi: 10.1073/pnas.1413234112. Epub 2014 Dec 24.
Transplantation of endothelial cells (ECs) is a promising therapeutic approach for ischemic disorders. In addition, the generation of ECs has become increasingly important for providing vascular plexus to regenerated organs, such as the liver. Although many attempts have been made to generate ECs from pluripotent stem cells and nonvascular cells, the minimum number of transcription factors that specialize in directly inducing vascular ECs remains undefined. Here, by screening 18 transcription factors that are important for both endothelial and hematopoietic development, we demonstrate that ets variant 2 (ETV2) alone directly converts primary human adult skin fibroblasts into functional vascular endothelial cells (ETVECs). In coordination with endogenous FOXC2 in fibroblasts, transduced ETV2 elicits expression of multiple key endothelial development factors, including FLI1, ERG, and TAL1, and induces expression of endothelial functional molecules, including EGFL7 and von Willebrand factor. Consequently, ETVECs exhibits EC characteristics in vitro and forms mature functional vasculature in Matrigel plugs transplanted in NOD SCID mice. Furthermore, ETVECs significantly improve blood flow recovery in a hind limb ischemic model using BALB/c-nu mice. Our study indicates that the creation of ETVECs provides further understanding of human EC development induced by ETV2.
内皮细胞(ECs)移植是一种治疗缺血性疾病的有前景的方法。此外,对于为诸如肝脏等再生器官提供血管丛而言,ECs的生成变得越来越重要。尽管已经进行了许多尝试来从多能干细胞和非血管细胞生成ECs,但专门直接诱导血管ECs的转录因子的最小数量仍未明确。在这里,通过筛选对内皮和造血发育都很重要的18种转录因子,我们证明单独的ets变体2(ETV2)可直接将原代人类成人皮肤成纤维细胞转化为功能性血管内皮细胞(ETVECs)。在成纤维细胞中与内源性FOXC2协同作用,转导的ETV2引发包括FLI1、ERG和TAL1在内的多种关键内皮发育因子的表达,并诱导包括EGFL7和血管性血友病因子在内的内皮功能分子的表达。因此,ETVECs在体外表现出EC特征,并在移植到NOD SCID小鼠体内的基质胶塞中形成成熟的功能性脉管系统。此外,ETVECs在使用BALB/c-nu小鼠的后肢缺血模型中显著改善了血流恢复。我们的研究表明,ETVECs的产生为进一步了解ETV2诱导的人类EC发育提供了依据。