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Alterations in ganglioside expression during the differentiation of human mast cells
Author(s) -
Zuberbier T.,
Guhl S.,
Hantke T.,
Hantke C.,
Welker P.,
Grabbe J.,
Henz B. M.
Publication year - 1999
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.1999.tb00386.x
Subject(s) - tryptase , ganglioside , mast cell , peripheral blood mononuclear cell , cellular differentiation , degranulation , biology , cell culture , immunoglobulin e , microbiology and biotechnology , cell , chemistry , immunology , antibody , receptor , biochemistry , in vitro , genetics , gene
Gangliosides are physiological components of the outer cell membrane. In the present study, the role of ganglioside expression during differentiation of human mast cells was evaluated. After 11 days of culture in medium known to induce mast cell differentiation, 70% of peripheral blood mononuclear cells (PBMC) showed positive staining for the high affinity IgE receptor and tryptase on immunocytochemistry and an associated 20‐fold increase of ganglioside GM3 expression. Furthermore, exogenous addition of GM3 during cultivation of PBMC in medium containing low levels of growth factors induced an increase of mast cell specific tryptase. The association of ganglioside expression with mast cell differentiation was confirmed by experiments with the human mast cell line HMC‐1. FcɛRI‐positive cultured cells enriched with immunobeads exhibited a 3‐fold higher expression of GM3, compared to FcɛRI negative HMC‐1 cells. Furthermore, measurable amounts of the gangliosides GM2, GM1 and GD1a were found only in the FcɛRI positive cells. A corresponding transient increase of mRNA for GalNAcT, the key enzyme in the production of these latter gangliosides, could be detected preceding the expression of these gangliosides and the FcɛRI by RT‐PCR. Taken together, these data point to a functional role of gangliosides in the differentiation of human mast cells.