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人DEC-205的cDNA克隆,DEC-205是一种假定的树突状细胞上的抗原摄取受体。

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

作者信息

Kato M, Neil T K, Clark G J, Morris C M, Sorg R V, Hart D N

机构信息

Hematology/Immunology/Transfusion Medicine Research Group, Christchurch School of Medicine, New Zealand.

出版信息

Immunogenetics. 1998 May;47(6):442-50. doi: 10.1007/s002510050381.

Abstract

Dendritic cells (DC) are specialist antigen presenting 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 reverse 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.

摘要

树突状细胞(DC)是专门的抗原呈递细胞,其在外周捕获抗原,向中枢迁移,并在主要组织相容性复合体和适当的共刺激分子的背景下将加工后的抗原呈递给T淋巴细胞以启动免疫反应。DEC-205已被鉴定为一种假定的抗原摄取受体,在小鼠DC上大量表达。最近克隆的小鼠DEC-205 cDNA预测的分子结构与巨噬细胞甘露糖受体有显著相似性。利用逆转录聚合酶链反应(RT-PCR)和cDNA文库筛选,我们从霍奇金病来源的L428细胞系中获得了人DEC-205 cDNA的完整编码区。预测的蛋白质结构是一种由1722个氨基酸组成的I型跨膜蛋白,由信号肽、富含半胱氨酸的结构域、II型纤连蛋白结构域、十个碳水化合物识别样结构域、跨膜结构域和细胞质尾组成。人DEC-205与小鼠蛋白的同源性为77%,半胱氨酸完全保守。通过体细胞杂交板分析和荧光原位杂交将DEC-205基因(LY75)定位于染色体带2q24。Northern印迹分析在髓系、B淋巴细胞系和霍奇金病来源的细胞系中检测到7.8和9.5千碱基的DEC-205转录本。RT-PCR分析表明,未成熟的血液DC含有几乎检测不到的DEC-205转录本,但在分化/激活后这些转录本显著增加。

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