Department of Signal Transduction, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Animal Resource Center for Infectious Diseases, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Dev Cell. 2015 May 4;33(3):247-59. doi: 10.1016/j.devcel.2015.02.024. Epub 2015 Apr 23.
Molecular pathways regulating the development of arterial and venous endothelial cells (ECs) are now well established, but control of parallel arterial-venous alignment is unclear. Here we report that arterial-venous alignment in the skin is determined by apelin receptor (APJ) expression in venous ECs. One of the activators of APJ is apelin. We found that apelin is produced by arterial ECs during embryogenesis, induces chemotaxis of venous ECs, and promotes the production of secreted Frizzled-related protein 1 (sFRP1) by APJ(+) ECs. sFRP1 stimulates matrix metalloproteinase production by Ly6B.2(+) neutrophil-like cells located between the arteries and veins, resulting in remodeling of extracellular matrices to support venous displacement. Moreover, using apelin- or APJ-deficient mice, which exhibit arterial-venous disorganization, we found that arterial-venous alignment is involved in thermoregulation, possibly by regulating countercurrent heat exchange. We hypothesize that the evolution of parallel juxtapositional arterial-venous alignment was an adaptation to reduce body heat loss.
分子途径调节动脉和静脉内皮细胞 (ECs) 的发育现在已经得到很好的建立,但并行的动静脉对准的控制尚不清楚。在这里,我们报告说,皮肤中的动静脉对准由静脉 ECs 中的阿片肽受体 (APJ) 表达决定。APJ 的激活剂之一是阿皮素。我们发现,阿皮素在胚胎发生过程中由动脉 ECs 产生,诱导静脉 ECs 的趋化性,并促进 APJ(+)ECs 产生分泌型卷曲相关蛋白 1 (sFRP1)。sFRP1 刺激位于动脉和静脉之间的 Ly6B.2(+)中性粒细胞样细胞产生基质金属蛋白酶,导致细胞外基质重塑,以支持静脉移位。此外,使用阿皮素或 APJ 缺陷小鼠,其表现出动静脉组织紊乱,我们发现动静脉对准涉及体温调节,可能通过调节逆流热交换来实现。我们假设平行并列动静脉对准的进化是一种适应,以减少身体热量损失。