Human epidermal Langerhans cells are selectively recognized by galectin-3 but not by galectin-1
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
11055799
Knihovny.cz E-resources
- MeSH
- Antigens, CD1 analysis immunology MeSH
- Antigens, CD analysis immunology MeSH
- Antigens, Differentiation immunology MeSH
- Adult MeSH
- Epitopes analysis MeSH
- Galectin 1 MeSH
- Galectin 3 MeSH
- Hemagglutinins immunology MeSH
- Keratinocytes cytology immunology MeSH
- Cells, Cultured MeSH
- Skin cytology immunology MeSH
- Langerhans Cells cytology immunology MeSH
- Lectins immunology MeSH
- Humans MeSH
- Binding Sites MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antigens, CD1 MeSH
- Antigens, CD MeSH
- Antigens, Differentiation MeSH
- Epitopes MeSH
- Galectin 1 MeSH
- Galectin 3 MeSH
- Hemagglutinins MeSH
- Lectins MeSH
Langerhans cells are dendritic antigen-presenting cells residing predominantly in the epidermis. Since endogenous galactoside-binding lectins with the jelly-roll motif (galectins) are known to trigger cellular responses, including mediator release, we investigated by lectin histochemistry the cells' capacity to bind two common members of this family, i.e. galectin-1 and -3. Actually, surrounding keratinocytes express a high level of galectin-3, and these cells can be considered as donors of this lectin to Langerhans cells. Employing biotinylated galectin-1 and -3, and concomitantly an antibody against CD1a as a second marker, to visualize the position of Langerhans cells in the human epidermis, the expression of galectin-3-reactive glycoligands in contrast to the lack of binding of galectin-1 was observed. Although the functional consequences of this selectivity are unclear, these results reveal an example for differential cellular reactivity towards two related endogenous lectins.