摘要
分化簇 (CD155) 以前被鉴定为脊髓灰质炎病毒受体 (PVR),后来被鉴定为免疫球蛋白分子,参与细胞粘附、增殖、侵袭和迁移。它是一种主要在正常和转化的恶性细胞上表达的表面蛋白。受体的表达因组织来源而异。该蛋白的表达由 sonic Hedgehog 通路、Ras-MEK-ERK 通路和压力条件(如 DNA 损伤反应)中涉及的因素决定。该蛋白质使用交替剪接机制,产生四种同工型,两种是可溶的(CD155β 和 CD155γ),另一种是跨膜蛋白(CD155α 和 CD155δ)。除了作为病毒受体外,研究人员还发现 CD155 在癌症研究和细胞信号传导领域发挥重要作用。该受体被认为是识别癌组织的生物标志物。该受体与参与细胞防御机制的分子相互作用。正在破译 CD155 的免疫监视作用,以了解它用作肿瘤免疫分子的机制方法。 CD155 是一种非 MHC-I 配体,有助于通过抑制性 TIGIT 配体识别 NK 细胞的非自身。 TIGIT-CD155 通路是一种新的 MHC-I 独立教育机制,用于细胞耐受和 NK 细胞的激活。该受体还在癌症转移和跨内皮机制中起作用。在这篇综述中,作者讨论了通过单个跨膜受体发生的病毒-宿主相互作用,即脊髓灰质炎病毒感染途径,该途径被用作治疗途径。溶瘤病毒疗法现在是治疗癌症的有前途的方式。
关键词: CD155、PVR、脊髓灰质炎病毒、癌症、PDGFR、VEGFR。
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