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CD63 促进了蛤中血细胞介导的吞噬作用。

CD63 Promotes Hemocyte-Mediated Phagocytosis in the Clam, .

机构信息

Engineering Research Center of Marine Biological Resource Comprehensive Utilization, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, China.

Department of Immunology and Pathogen Biology, Zunyi Medical College, Zhuhai Campus, Zhuhai 519041, China.

出版信息

J Immunol Res. 2016;2016:7893490. doi: 10.1155/2016/7893490. Epub 2016 Oct 27.

DOI:10.1155/2016/7893490
PMID:27868074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5102739/
Abstract

As one of the surface membrane proteins of tetraspanin family, CD63 plays a crucial role in cellular trafficking and endocytosis, which also is associated with activation of a wide variety of immune cells. Here, the homolog of CD63 was characterized from one marine mollusk, , which is designated as Pu-CD63. The complete cDNA of Pu-CD63 is 1,738 bp in length with an open reading frame (ORF) of 849 bp, encoding a 282 amino acid protein with four putative hydrophobic transmembrane helixes. Bioinformatic analysis revealed that Pu-CD63 contains one putative YXXØ consensus motif of "110-YVII-113" and one N-glycosylation site "155-NGT-157" within the large extracellular loop (LEL) region, supporting its conserved function in plasma membrane and endosomal/lysosomal trafficking. Moreover, temporal expression profile analysis demonstrates a drastic induction in the expression of CD63 in hemocytes after pathogenic challenge with either or . By performing dsRNA-mediate RNAi knockdowns of CD63, a dramatic reduction in hemocytes phagocytic activity to pathogenic is recorded by flow cytometry, revealing the definite role of Pu-CD63 in promoting hemocyte-mediated phagocytosis. Therefore, our work has greatly enhanced our understanding about primitive character of innate immunity in marine mollusk.

摘要

作为四跨膜蛋白家族的表面膜蛋白之一,CD63 在细胞运输和内吞作用中起着至关重要的作用,这也与多种免疫细胞的激活有关。在这里,我们从一种海洋软体动物中鉴定出了 CD63 的同源物,将其命名为 Pu-CD63。Pu-CD63 的完整 cDNA 长 1738bp,开放阅读框(ORF)长 849bp,编码一个由 282 个氨基酸组成的蛋白质,其中包含四个假定的疏水性跨膜螺旋。生物信息学分析表明,Pu-CD63 在大的细胞外环(LEL)区域内包含一个假定的 YXXØ 共识基序“110-YVII-113”和一个 N-糖基化位点“155-NGT-157”,支持其在质膜和内体/溶酶体运输中的保守功能。此外,时间表达谱分析表明,在受到 或 感染后,血细胞中 CD63 的表达急剧增加。通过进行 dsRNA 介导的 CD63 RNAi 敲低,流式细胞术记录到血细胞对病原体的吞噬活性明显降低,表明 Pu-CD63 在促进血细胞介导的吞噬作用中具有明确的作用。因此,我们的工作大大增强了我们对海洋软体动物先天免疫原始特征的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/5102739/ad139ac18c48/JIR2016-7893490.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/5102739/dd96464c456d/JIR2016-7893490.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/5102739/ad139ac18c48/JIR2016-7893490.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/5102739/dd96464c456d/JIR2016-7893490.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/5102739/ad139ac18c48/JIR2016-7893490.002.jpg

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