cDNA cloning of human DEC-205, a putative antigen-uptake receptor on dendritic cells

被引:58
作者
Kato, M
Neil, TK
Clark, GJ
Morris, CM
Sorg, RV
Hart, DNJ
机构
[1] Christchurch Sch Med, Hematol Immunol Transfus Med Res Grp, Christchurch 8030, New Zealand
[2] Christchurch Sch Med, Cytogenet & Mol Oncol Unit, Christchurch 8030, New Zealand
关键词
antigen presenting cells; dendritic cells; cell surface molecule; antigen receptor; human;
D O I
10.1007/s002510050381
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dendritic cells (DC) are specialist antigen pre senting cells which capture antigens in the periphery, migrate centrally, and present the processed antigens in the context of major histocompatibility complex and appropriate co-stimulatory molecules to T lymphocytes for the initiation of an immune response. DEC-205 has been identified as a putative antigen-uptake receptor, which is expressed abundantly on mouse DC. The recently cloned mouse DEC-205 cDNA predicts a molecular structure which has a marked similarity to the macrophage mannose receptor. Using re verse transcriptase-polymerase chain reaction (RT-PCR) and cDNA library screening, we obtained the full coding region of human DEC-205 cDNA from the Hodgkin's disease-derived L428 cell line. The predicted protein structure is a type I transmembrane protein of 1722 amino acids consisting of a signal peptide, cysteine-rich domain, fibronectin type II domain, ten carbohydrate recognition-like domains, transmembrane domain, and a cytoplasmic tail. Human DEC-205 is 77% identical to the mouse protein with completely conserved cysteines. The DEC-205 gene (LY75) was mapped to chromosome band 2q24 by somatic cell hybrid panel analysis and fluorescent in situ hybridization. Northern blot analysis detected 7.8 and 9.5 kilobase DEC-205 transcripts in myeloid, B lymphoid, and Hodgkin's disease-derived cell lines. RT-PCR analysis indicated that immature blood DC contain a barely detectable amount of DEC-205 transcripts but these were markedly increased upon differentiation/activation.
引用
收藏
页码:442 / 450
页数:9
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