Kwakkenbos Mark J, Kop Else N, Stacey Martin, Matmati Mourad, Gordon Siamon, Lin Hsi-Hsien, Hamann Jörg
Laboratory for Experimental Immunology, Academic Medical Center, University of Amsterdam, G1-106, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
Immunogenetics. 2004 Jan;55(10):655-66. doi: 10.1007/s00251-003-0625-2. Epub 2003 Nov 27.
With the human and mouse genome projects now completed, the receptor repertoire of mammalian cells has finally been elucidated. The EGF-TM7 receptors are a family of class B seven-span transmembrane (TM7) receptors predominantly expressed by cells of the immune system. Within the large TM7 superfamily, the molecular structure and ligand-binding properties of EGF-TM7 receptors are unique. Derived from the processing of a single polypeptide, they are expressed at the cell surface as heterodimers consisting of a large extracellular region associated with a TM7 moiety. Through a variable number of N-terminal epidermal growth factor (EGF)-like domains, EGF-TM7 receptors interact with cellular ligands such as CD55 and chondroitin sulfate. Recent in vivo studies demonstrate a role of the EGF-TM7 receptor CD97 in leukocyte migration. The different number of EGF-TM7 genes in man compared with mice, the chimeric nature of EMR2 and the inactivation of human EMR4 point toward a still-evolving receptor family. Here we discuss the currently available information on this intriguing receptor family.
随着人类和小鼠基因组计划的完成,哺乳动物细胞的受体库终于得以阐明。表皮生长因子七次跨膜(EGF-TM7)受体是B类七次跨膜(TM7)受体家族,主要由免疫系统细胞表达。在庞大的TM7超家族中,EGF-TM7受体的分子结构和配体结合特性独具特色。它们由单一多肽加工而来,在细胞表面以异二聚体形式表达,由一个与TM7部分相关的大细胞外区域组成。通过可变数量的N端表皮生长因子(EGF)样结构域,EGF-TM7受体与细胞配体如CD55和硫酸软骨素相互作用。最近的体内研究表明EGF-TM7受体CD97在白细胞迁移中发挥作用。与小鼠相比,人类中EGF-TM7基因数量不同,EMR2的嵌合性质以及人类EMR4的失活表明该受体家族仍在不断进化。在此,我们讨论关于这个有趣受体家族的现有信息。