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Differentiation-dependent glycosylation of cells in squamous cell epithelia detected by a mammalian lectin.
- Source :
-
Cells, tissues, organs [Cells Tissues Organs] 2002; Vol. 171 (2-3), pp. 135-44. - Publication Year :
- 2002
-
Abstract
- Unlabelled: The squamous stratified epithelia contain a proliferative (harboring mitotic activity) and a differentiating compartment. Due to the potential of protein-carbohydrate interactions to regulate cellular activities we introduced a mammalian lectin to cyto- and histochemical analysis. We answer the questions of whether and to what extent this new probe can pinpoint differentiation-dependent glycosylation changes in sections and in culture of keratinocytes.<br />Material and Methods: Purification and labeling enabled monitoring of galectin-3 reactivity in frozen sections of human and pig epidermis and basal cell carcinomas as well as in culture of keratinocytes. The staining pattern of the lectin was correlated with the staining profile of other cell markers including desmosomal proteins, beta(1) integrin, and the proliferation marker Ki-67. The Dolichos biflorus agglutinin (DBA) sharing binding reactivity of galectin-3 to the A type histoblood group epitope was used for comparison.<br />Results: Both lectins exhibit suprabasal binding. However, their profiles were not identical, substantiated by lack of coinhibition. Strong DBA reactivity was also observed in a limited number of basal layer cells, namely in cells without the expression of the proliferation marker Ki-67. Cultured mitotic epidermal cells have no reactivity for DBA. Presence of ligands for this plant lectin was connected with decreased positivity of nuclei for Ki-67 and the occurrence of ring-shaped nucleoli, micronucleoli or absence of nucleoli. Considering colocalization the pattern of galectin-3-binding sites coincided with the presence of desmosomal proteins such as desmoplakin-1 and desmoglein but not beta(1) integrin, a potential ligand. Interestingly, studied basal cell carcinomas expressed no binding sites for galectin-3, while a limited number of cells were DBA-reactive.<br />Conclusion: The expression of galectin-3-binding sites and also DBA-reactive glycoligands correlates with an increased level of differentiation and/or cessation of proliferation in the examined squamous stratified epithelia. Further application of tissue lectins for characterizing ligand expression and its modulation is an important step to reveal functional relevance.<br /> (Copyright 2002 S. Karger AG, Basel)
- Subjects :
- Animals
Binding Sites
Carcinoma, Basal Cell metabolism
Cells, Cultured
Cytoskeletal Proteins metabolism
Desmogleins
Desmoplakins
Epithelial Cells cytology
Glycosylation
Humans
Immunohistochemistry
Integrin beta1 metabolism
Keratinocytes cytology
Keratinocytes metabolism
Keratins metabolism
Ki-67 Antigen metabolism
Mice
Plant Lectins metabolism
Protein Binding
Skin Neoplasms metabolism
Swine
Cell Differentiation physiology
Epithelial Cells metabolism
Epithelium physiology
Galectin 3 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1422-6405
- Volume :
- 171
- Issue :
- 2-3
- Database :
- MEDLINE
- Journal :
- Cells, tissues, organs
- Publication Type :
- Academic Journal
- Accession number :
- 12097836
- Full Text :
- https://doi.org/10.1159/000063707