| Content Provider |
World Health Organization (WHO)-Global Index Medicus |
| Author |
Tsou, Yun-ting Pai, Feng-shuo Chen, Chung-hsuan Hsieh, Shie-liang Yang, Wen-bin Hsu, Tsui-ling Huang, Ya-lang Wu, Chung-yi Wong, Chi-huey Chou, Teh-ying Mon, Hsien-chen |
| Description |
Author Affiliation: Huang YL ( From the Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.); Pai FS ( the Institute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei.); Tsou YT ( From the Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.); Mon HC ( National Yang-Ming University School of Medicine, Taipei.); Hsu TL ( the Genomics Research Center, Academia Sinica, Taipei.); Wu CY ( the Genomics Research Center, Academia Sinica, Taipei.); Chou TY ( the Institute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei.); Yang WB ( the Genomics Research Center, Academia Sinica, Taipei.); Chen CH ( the Genomics Research Center, Academia Sinica, Taipei.); Wong CH ( the Genomics Research Center, Academia Sinica, Taipei.); Hsieh SL ( From the Institute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan, the Institute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei, the Genomics Research Center, Academia Sinica, Taipei, the Department of Medical Research and Education, Tai) |
| Abstract |
The human C-type lectin 18 (clec18) gene cluster, which contains three clec18a, clec18b, and clec18c loci, is located in human chromosome 16q22. Although the amino acid sequences of CLEC18A, CLEC18B, and CLEC18C are almost identical, several amino acid residues located in the C-type lectin-like domain (CTLD) and the sperm-coating protein/Tpx-1/Ag5/PR-1/Sc7 (SCP/TAPS) domain, also known as the cysteine-rich secretory proteins/antigen 5/pathogenesis-related 1 proteins (CAP) domain, are distinct from each other. Genotyping by real-time PCR and sequencing further shows the presence of multiple alleles in clec18a/b/c loci. Flow cytometry analysis demonstrates that CLEC18 (CLEC18A, -B, and -C) are expressed abundantly in human peripheral blood cells. Moreover, CLEC18 expression is further up-regulated when monocytes differentiate into macrophages and dendritic cells. Immunofluorescence staining reveals that CLEC18 are localized in the endoplasmic reticulum, Golgi apparatus, and endosome. Interestingly, CLEC18 are also detectable in human sera and culture supernatants from primary cells and 293T cells overexpressing CLEC18. Moreover, CLEC18 bind polysaccharide in Ca(2+)-independent manner, and amino acid residues Ser/Arg(339) and Asp/Asn(421) in CTLD domain contribute to their differential binding abilities to polysaccharides isolated from Ganoderma lucidum (GLPS-F3). The Ser(339) (CLEC18A) â Arg(339) (CLEC18A-1) mutation completely abolishes CLEC18A-1 binding to GLPS-F3, and a sugar competition assay shows that CLEC18 preferentially binds to fucoidan, ß-glucans, and galactans. Because proteins with the SCP/TAPS/CAP domain are able to bind sterol and acidic glycolipid, and are involved in sterol transport and ß-amyloid aggregation, it would be interesting to investigate whether CLEC18 modulates host immunity via binding to glycolipids, and are also involved in glycolipid transportation and protein aggregation in the future. |
| ISSN |
00219258 |
| e-ISSN |
1083351X |
| Journal |
Journal of Biological Chemistry |
| Issue Number |
35 |
| Volume Number |
290 |
| Language |
English |
| Publisher |
American Society for Biochemistry and Molecular Biology (United States) |
| Publisher Date |
2015-08-28 |
| Publisher Place |
United States |
| Access Restriction |
Open |
| Subject Keyword |
Lectins, C-Type Genetics Multigene Family Polysaccharides Metabolism Amino Acid Sequence Cell Line Cells, Cultured Molecular Sequence Data Protein Binding Sequence Alignment Research Support, Non-U.S. Gov't Biochemistry Molecular Biology |
| Content Type |
Text |
| Resource Type |
Article |
| Subject |
Cell Biology Biochemistry Molecular Biology |
