6533b7d5fe1ef96bd12648b2
RESEARCH PRODUCT
Subtypes of non-transformed human mammary epithelial cells cultured in vitro: histo-blood group antigen H type 2 defines basal cell-derived cells.
B VojtesekHenrik ClausenE. B. LaneRoland MollMichael KasperG. PapsdorfUwe KarstenA. PaulyPeter Stosieksubject
AdultCancer ResearchCell typeIsoantigensmedicine.drug_classImmunocytochemistryMolecular Sequence DataBiologyMonoclonal antibodyEpitopeEpitheliumCell LineCytokeratinAntigenAntigens NeoplasmmedicineHumansElectrophoresis Gel Two-DimensionalBreastMolecular BiologyThomsen-Friedenreich AntigenEpithelial CellsCell BiologyMolecular biologyImmunohistochemistryClone CellsCarbohydrate SequenceCell cultureFemaleDevelopmental Biologydescription
Normal (non-transformed) human mammary epithelial cell lines derived from reduction mammoplasties were analyzed by immunocytochemistry with more than 80 monoclonal antibodies (mAbs) and other specific reagents to tissue-specific and developmentally regulated antigens at different passage levels. A subpopulation of poorly differentiated, proliferating epithelial cells, corresponding to the 'selected' cell type of late passages, is shown to be characterized by a new marker, the histo-blood group antigen H type 2, probably carried on a membrane-bound glycolipid. These cells also express a number of other onco-developmental carbohydrate antigens [Le(y), Le(x), sialosyl-Le(a), precursor of Thomsen Friedenreich antigen (Tn), but not Thomsen-Friedenreich antigen and sialosyl-Tn]. Their cytokeratin (CK) phenotype, as assessed by reactivity with monospecific mAbs and two-dimensional gel electrophoresis, is CK 5, 6, 14 and 17, with CK 19 being consistently absent, and varying minor amounts of CK 7, 8 and 18, as well as 15 and 16. The reactivity of these cells with a panel of 11 mAbs specific for CK 18 varies considerably even after cloning, indicating heterogeneity of epitope expression or accessibility. Our data strongly suggest that the H type 2+ cells develop from the basal cell layer of the mammary gland.
year | journal | country | edition | language |
---|---|---|---|---|
1993-08-01 | Differentiation; research in biological diversity |