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The EGF-TM7 family: a postgenomic view
Authors:Mark?J?Kwakkenbos  Else?N?Kop  Martin?Stacey  Mourad?Matmati  Siamon?Gordon  Hsi-Hsien?Lin  Email author" target="_blank">J?rg?HamannEmail author
Institution:(1) Laboratory for Experimental Immunology, Academic Medical Center, University of Amsterdam, G1-106, P.O. Box 22700, 1100 DE Amsterdam, The Netherlands;(2) Division of Clinical Immunology and Rheumatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands;(3) Sir William Dunn School of Pathology, University of Oxford, Oxford, UK
Abstract: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.
Keywords:CD97  Class B GPCR  EMR  GPS  LNB-TM7 family
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