The EGF-TM7 family: a postgenomic view

被引:110
作者
Kwakkenbos, MJ
Kop, EN
Stacey, M
Matmati, M
Gordon, S
Lin, HH
Hamann, J
机构
[1] Univ Amsterdam, Acad Med Ctr, Expt Immunol Lab, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Div Clin Immunol & Rheumatol, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金;
关键词
CD97; class B GPCR; EMR; GPS; LNB-TM7; family;
D O I
10.1007/s00251-003-0625-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:655 / 666
页数:12
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