Ezumi Y, Uchiyama T, Takayama H
Department of Hematology and Oncology, Clinical Sciences for Pathological Organs, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawaracho, Sakyo-ku, Kyoto, 606-8507, Japan.
Biochem Biophys Res Commun. 2000 Oct 14;277(1):27-36. doi: 10.1006/bbrc.2000.3624.
Glycoprotein VI (GPVI) is the major collagen receptor underlying platelet activation. We cloned the full-length cDNA for GPVI (GPVI-1) and its two isoforms (GPVI-2 and -3) from phorbol-ester-stimulated CMK cells. The GPVI-1 cDNA was identical in the coding region with the cDNA that has recently been reported to belong to the immunoglobulin superfamily. The GPVI gene consisted of 8 exons spanning over 23 kbp and was mapped on the chromosome 19q13. 4. The promoter of GPVI gene lacked TATA and CAAT boxes and had multiple transcription start sites like other megakaryocytic genes. When COS-7 cells were cotransfected with the GPVI isoforms and Fc receptor gamma chain, Fc receptor gamma chain was associated with GPVI-1 and -2 but did not affect the GPVI expression levels. GPVI-1 and -2 could bind the collagen-related peptide, which exhibits triple-helical and polymeric structure of collagen to activate platelets via GPVI.
糖蛋白VI(GPVI)是血小板激活的主要胶原受体。我们从佛波酯刺激的CMK细胞中克隆了GPVI的全长cDNA(GPVI-1)及其两种异构体(GPVI-2和-3)。GPVI-1 cDNA在编码区与最近报道的属于免疫球蛋白超家族的cDNA相同。GPVI基因由8个外显子组成,跨越23kbp,定位于19号染色体q13.4。GPVI基因的启动子缺乏TATA和CAAT框,并且像其他巨核细胞基因一样有多个转录起始位点。当COS-7细胞与GPVI异构体和Fc受体γ链共转染时,Fc受体γ链与GPVI-1和-2相关,但不影响GPVI的表达水平。GPVI-1和-2可以结合胶原相关肽,该肽呈现胶原的三螺旋和多聚体结构,通过GPVI激活血小板。