Deletion polymorphism of SIGLEC14 and its functional implications

Glycobiology. 2009 Aug;19(8):841-6. doi: 10.1093/glycob/cwp052. Epub 2009 Apr 15.

Abstract

Human Siglec-14, a member of the Siglec family of sialic acid-binding lectins, shows extensive sequence similarity to human Siglec-5. To analyze respective expression patterns of Siglec-14 and Siglec-5, we developed specific antibodies against each of them. We found that the former was expressed on granulocytes and monocytes, while the latter was on granulocytes and B-cells. Surprisingly, some individuals lacked the expression of Siglec-14, while they all expressed Siglec-5. We found that a fusion between SIGLEC14 and SIGLEC5 genes, resulting in the functional deletion of SIGLEC14, underlies this phenotype. The presence of the "SIGLEC14 null" allele in all human populations we tested implies an ancient origin, while its allelic frequency is higher in Asians compared with Africans and Europeans. The forced expression of Siglec-14 in a monocytic cell line-enhanced TNF-alpha secretion elicited by lipopolysaccharide. These results imply that Siglec-14 may play some role in bacterial infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / genetics
  • Antigens, CD / metabolism*
  • Antigens, Differentiation, Myelomonocytic / genetics
  • Antigens, Differentiation, Myelomonocytic / metabolism*
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Cell Differentiation / physiology
  • Cell Line
  • Gene Fusion
  • Granulocytes / immunology
  • Granulocytes / metabolism
  • Humans
  • Lectins / genetics
  • Lectins / metabolism*
  • Lipopolysaccharides / pharmacology
  • Macrophages / cytology
  • Macrophages / metabolism
  • Monocytes / immunology
  • Monocytes / metabolism
  • Polymorphism, Genetic*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Lectins
  • Lipopolysaccharides
  • Receptors, Cell Surface
  • SIGLEC14 protein, human
  • SIGLEC5 protein, human
  • Tumor Necrosis Factor-alpha