Nakayama Hironao, Kusumoto Chiaki, Nakahara Masako, Fujiwara Akira, Higashiyama Shigeki
Department of Medical Science and Technology, Hiroshima International University, Higashihiroshima, Japan.
Division of Cell Growth and Tumor Regulation, Proteo-Science Center, Ehime University, Toon, Japan.
Front Physiol. 2018 Nov 23;9:1662. doi: 10.3389/fphys.2018.01662. eCollection 2018.
Axon guidance molecules play an important role in regulating proper neuronal networking during neuronal development. They also have non-neuronal properties, which include angiogenesis, inflammation, and tumor development. Semaphorin 3F (SEMA3F), a member of the class 3 semaphorins, was initially identified as an axon guidance factor, that repels axons and collapses growth cones. However, SEMA3F has similar effects on endothelial cells (ECs) and tumor cells. In this review, we discuss the novel molecular mechanisms underlying SEMA3F activity in vascular and tumor biology. Recent evidence suggests that SEMA3F functions as a PI3K-Akt-mTOR inhibitor in mammalian cells, including T cells, ECs, and tumor cells. Therefore, SEMA3F may have broad therapeutic implications. We also discuss the key role of axon guidance molecules as regulators of the tumor microenvironment. Netrin-1, a chemoattractant factor in the neuronal system, promotes tumor progression by enhancing angiogenesis and metastasis. Moreover, our recent studies demonstrate that netrin-1/neogenin interactions augment CD4+ T cell chemokinesis and elicit pro-inflammatory responses, suggesting that netrin-1 plays a key role in modulating the function of a tumor and its surrounding cells in the tumor microenvironment. Overall, this review focuses on SEMA3F and netrin-1 signaling mechanisms to understand the diverse biological functions of axon guidance molecules.
轴突导向分子在神经元发育过程中调节适当的神经网络方面发挥着重要作用。它们还具有非神经元特性,包括血管生成、炎症和肿瘤发展。3型信号素3F(SEMA3F)是3型信号素家族的成员,最初被鉴定为一种轴突导向因子,它排斥轴突并使生长锥塌陷。然而,SEMA3F对内皮细胞(ECs)和肿瘤细胞有类似的作用。在这篇综述中,我们讨论了SEMA3F在血管和肿瘤生物学中活性的新分子机制。最近的证据表明,SEMA3F在包括T细胞、内皮细胞和肿瘤细胞在内的哺乳动物细胞中作为PI3K-Akt-mTOR抑制剂发挥作用。因此,SEMA3F可能具有广泛的治疗意义。我们还讨论了轴突导向分子作为肿瘤微环境调节因子的关键作用。Netrin-1是神经系统中的一种化学吸引因子,通过增强血管生成和转移促进肿瘤进展。此外,我们最近的研究表明,netrin-1/neogenin相互作用增强CD4+T细胞的趋化作用并引发促炎反应,这表明netrin-1在调节肿瘤微环境中肿瘤及其周围细胞的功能方面起关键作用。总体而言,这篇综述聚焦于SEMA3F和netrin-1信号机制,以了解轴突导向分子的多种生物学功能。