Laboratory of Immunogenetics, Department of Medical Sciences, University of Torino, Via Santena 19, 10126 Torino, Italy.
Front Biosci (Landmark Ed). 2014 Jan 1;19(2):366-78. doi: 10.2741/4213.
CD157 is a member of the ADP-ribosyl cyclase gene family that is involved in the metabolism of NAD. CD157 behaves both as an ectoenzyme and as a receptor. Though CD157 is anchored to the membrane by a glycosylphosphatidylinositol moiety, which makes it unsuitable to transduce signals on its own, it exploits its localization in selected membrane microdomains and its proclivity to interact with integrins to accomplish receptor functions. Initially characterized as a stromal and myeloid antigen involved in the control of leukocyte adhesion, migration and diapedesis, CD157 was subsequently found to have a far wider distribution. In particular, CD157 was found to be expressed by epithelial ovarian cancer cells where it is involved in interactions among tumor cells, extracellular matrix proteins and mesothelium. The overall picture inferred from experimental and clinical observations is that CD157 is a critical player both in leukocyte trafficking and in ovarian cancer invasion and metastasis formation. In this review, we will discuss the biological mechanisms underpinning the role of CD157 in the control of leukocyte migration and ovarian cancer dissemination.
CD157 是 ADP-ribosyl 环化酶基因家族的一员,参与 NAD 的代谢。CD157 既是一种外切酶,也是一种受体。虽然 CD157 通过糖基磷脂酰肌醇部分锚定在膜上,使其本身不适合传递信号,但它利用其在选定的膜微区的定位和与整合素相互作用的倾向来完成受体功能。CD157 最初被描述为一种参与白细胞黏附、迁移和渗出控制的基质和髓样抗原,随后发现它的分布范围更广。特别是,CD157 在卵巢癌细胞中表达,在那里它参与肿瘤细胞、细胞外基质蛋白和间皮之间的相互作用。从实验和临床观察中推断出的总体情况是,CD157 是白细胞迁移和卵巢癌侵袭转移形成的关键参与者。在这篇综述中,我们将讨论 CD157 在控制白细胞迁移和卵巢癌细胞扩散中的作用的生物学机制。