Graduate School of International Agricultural Technology and Institutes of Green-Bio Science and Technology, Seoul National University, 1447 Pyeongchang-daero, Pyeongchang, Gangwon-do, 25354, Republic of Korea.
Department of Molecular and Cellular Physiology, Louisiana State University Health Science Center, 1501 Kings Highway, Shreveport, LA, 71103, USA.
Stem Cell Res Ther. 2023 Mar 16;14(1):41. doi: 10.1186/s13287-023-03267-x.
Extensive efforts have been made to achieve vascular regeneration accompanying tissue repair for treating vascular dysfunction-associated diseases. Recent advancements in stem cell biology and cell reprogramming have opened unforeseen opportunities to promote angiogenesis in vivo and generate autologous endothelial cells (ECs) for clinical use. We have, for the first time, identified a unique endothelial-specific transcription factor, ETV2/ER71, and revealed its essential role in regulating endothelial cell generation and function, along with vascular regeneration and tissue repair. Furthermore, we and other groups have demonstrated its ability to directly reprogram terminally differentiated non-ECs into functional ECs, proposing ETV2/ER71 as an effective therapeutic target for vascular diseases. In this review, we discuss the up-to-date status of studies on ETV2/ER71, spanning from its molecular mechanism to vasculo-angiogenic role and direct cell reprogramming toward ECs. Furthermore, we discuss future directions to deploy the clinical potential of ETV2/ER71 as a novel and potent target for vascular disorders such as cardiovascular disease, neurovascular impairment and cancer.
人们已经做出了广泛的努力来实现伴随组织修复的血管再生,以治疗与血管功能障碍相关的疾病。干细胞生物学和细胞重编程的最新进展为促进体内血管生成和生成用于临床的自体内皮细胞 (EC) 开辟了前所未有的机会。我们首次鉴定了一种独特的内皮特异性转录因子 ETV2/ER71,并揭示了它在调节内皮细胞生成和功能、血管再生和组织修复中的重要作用。此外,我们和其他小组已经证明它能够直接将终末分化的非 EC 重编程为功能性 EC,提出 ETV2/ER71 作为血管疾病的有效治疗靶点。在这篇综述中,我们讨论了 ETV2/ER71 的最新研究现状,涵盖了从其分子机制到血管生成作用以及向 EC 的直接细胞重编程。此外,我们讨论了未来的方向,以利用 ETV2/ER71 的临床潜力,将其作为心血管疾病、神经血管损伤和癌症等血管疾病的新型有效靶点。