Numasaki Muneo, Tsukamoto Hiroki, Tomioka Yoshihisa, Nishioka Yasuhiko, Ohrui Takashi
Laboratory of Clinical Science and Biomedicine, Faculty of Pharmaceutical Sciences, Josai University.
Tohoku J Exp Med. 2016 Sep;240(1):47-56. doi: 10.1620/tjem.240.47.
The interleukin (IL)-17 family, consisting of six homodimeric cytokines IL-17A, IL-17B, IL-17C, IL-17D, IL-17E/IL-25, and IL-17F, mediates a variety of biological activities including regulation of chemokine secretion and angiogenesis. Among the IL-17 family members, IL-17A and IL-17E/IL-25 are angiogenesis stimulators, while IL-17B and IL-17F are angiogenesis inhibitors. Recently, IL-17A/F heterodimer, comprised of the IL-17A and IL-17F subunits, was found as another member of the IL-17 cytokine family. However, to date, it has been unknown whether IL-17A/F has biological actions to affect the angiogenesis-related vascular endothelial functions. Therefore, in this study, we investigated the biological effects of IL-17A/F on the growth, migration and capillary-like tube formation of vascular endothelial cells. Recombinant IL-17A/F protein had no direct effects on the growth of human dermal microvascular endothelial cells (HMVECs), whereas, after 4-hour incubation in a modified Boyden Chemotaxicell chamber, IL-17A/F significantly induced migration of HMVECs over a wide range of doses via the phosphatidylinositol-3 kinase (PI3K) signaling pathway. We further investigated the biological effect of IL-17A/F on capillary-like tube formation using a co-culture system of human umbilical vein endothelial cells (HUVECs) and human dermal fibroblasts (HDFs), which mimicked the in vivo microenvironment. In this co-culture system, IL-17A/F significantly promoted capillary-like endothelial tube formation in a dose-dependent fashion via the PI3K and extracellular signal-regulated kinase (ERK) signaling pathways. Additionally, IL-17A/F up-regulated secretion of angiogenic growth factors such as IL-8 and growth-related oncogene (GRO)-α by HDFs. These findings identify a novel biological function for IL-17A/F as an indirect angiogenic agent.
白细胞介素(IL)-17家族由六种同型二聚体细胞因子IL-17A、IL-17B、IL-17C、IL-17D、IL-17E/IL-25和IL-17F组成,介导多种生物学活性,包括调节趋化因子分泌和血管生成。在IL-17家族成员中,IL-17A和IL-17E/IL-25是血管生成刺激因子,而IL-17B和IL-17F是血管生成抑制剂。最近,由IL-17A和IL-17F亚基组成的IL-17A/F异二聚体被发现是IL-17细胞因子家族的另一个成员。然而,迄今为止,尚不清楚IL-17A/F是否具有影响血管生成相关血管内皮功能的生物学作用。因此,在本研究中,我们研究了IL-17A/F对血管内皮细胞生长、迁移和毛细血管样管形成的生物学效应。重组IL-17A/F蛋白对人真皮微血管内皮细胞(HMVECs)的生长没有直接影响,然而,在改良的博伊登趋化小室中孵育4小时后,IL-17A/F通过磷脂酰肌醇-3激酶(PI3K)信号通路在很宽的剂量范围内显著诱导HMVECs迁移。我们进一步使用人脐静脉内皮细胞(HUVECs)和人真皮成纤维细胞(HDFs)的共培养系统研究了IL-17A/F对毛细血管样管形成的生物学效应,该系统模拟了体内微环境。在这个共培养系统中,IL-17A/F通过PI3K和细胞外信号调节激酶(ERK)信号通路以剂量依赖的方式显著促进毛细血管样内皮管的形成。此外,IL-17A/F上调了HDFs分泌血管生成生长因子如IL-8和生长相关癌基因(GRO)-α的水平。这些发现确定了IL-17A/F作为间接血管生成剂的一种新的生物学功能。