Ishimaru Tomohiro, Ishida Junji, Kim Jun-Dal, Mizukami Hayase, Hara Kanako, Hashimoto Misuzu, Yagami Ken-Ichi, Sugiyama Fumihiro, Fukamizu Akiyoshi
Graduate School of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572, Japan.
Life science Center, Tsukuba Advanced Research Alliance, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan.
J Biochem. 2017 Mar 1;161(3):255-258. doi: 10.1093/jb/mvw095.
Protein arginine methyltransferase 1 (PRMT1) is involved in multiple cellular functions including proliferation and differentiation. Although PRMT1 is expressed in vascular endothelial cells (ECs), which are responsible for angiogenesis during embryonic development, its role has remained elusive. In this study, we generated endothelial-specific prmt1-knockout (Prmt1-ECKO) mice, and found that they died before embryonic day 15. The superficial temporal arteries in these embryos were poorly perfused with blood, and whole-mount 3D imaging revealed dilated and segmentalized luminal structures in Prmt1-ECKO fetuses in comparison with those of controls. Our findings provide evidence that PRMT1 is important for embryonic vascular formation.
蛋白质精氨酸甲基转移酶1(PRMT1)参与多种细胞功能,包括增殖和分化。尽管PRMT1在血管内皮细胞(ECs)中表达,而血管内皮细胞在胚胎发育过程中负责血管生成,但其作用仍不清楚。在本研究中,我们构建了内皮细胞特异性prmt1基因敲除(Prmt1-ECKO)小鼠,发现它们在胚胎第15天之前死亡。这些胚胎的颞浅动脉血液灌注不良,与对照组相比,整体三维成像显示Prmt1-ECKO胎儿的管腔结构扩张且呈节段性。我们的研究结果证明PRMT1对胚胎血管形成很重要。