Blood group substances as differentiation markers in human dento‐gingival epithelium
Author(s) -
Steffensen B.,
Lopatin D. E.,
Caffesse R. G.,
Hanks C. T.
Publication year - 1987
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.1987.tb02054.x
Subject(s) - epithelium , junctional epithelium , cellular differentiation , basal (medicine) , immunofluorescence , cell type , biology , oral mucosa , pathology , cell , immunology , antibody , endocrinology , anatomy , medicine , biochemistry , gene , insulin
The level of cellular differentiation of human oral, sulcular, and junctional epithelium was compared by immunohistochemical analysis of cell membrane‐associated blood group‐specific carbohydrates. Identification of the blood group A‐specific carbohydrate and its two immediate precursor substances, type 2 chain H and N‐acetyllactosamine, was accomplished by an indirect immunofluorescence technique. Murine monoclonal antibodies reacting specifically with the antigenic determinants of the blood group substances were used as markers. The blood group A substance, indicating the highest level of cellular differentiation, was demonstrated on the cells in the upper layers of the oral epithelium. In the sulcular epithelium, the A substance was present on a few cells only, while type 2 chain H was observed frequently. This indicates an intermediate differentiation level of sulcular epithelium. The type 2 chain H precursor, N‐acetyllactosamine, the indicator of the lowest level of cell differentiation among the tested substances, was the only blood group substance detected on the junctional epithelial cells and on the basal cells of the sulcular and oral epithelium. Based upon previous studies of cell renewal and differentiation in oral epithelium, the present results indicate that the variations in distribution of the different blood group substances correspond with the regional rates of cell division and the levels of cellular differentiation. The findings also suggest that the cells in the junctional epithelium differentiate to a level similar to that of basal cells in the oral epithelium.