
The ability of cytokines (IFN alpha, IFN gamma, TNF alpha, IL-1 alpha, IL-6), all-trans retinoic acid, 1,25(OH)2-vitamin D3 and the tumor promoting phorbol ester TPA to regulate cell surface expression of protectin (CD59 antigen) on human hematopoietic and non-hematopoietic neoplastic cell lines was examined with the aid of immunocytofluorometric measurements. The tumor promoting phorbol ester TPA induced a marked up-regulation of protectin in all examined cell lines with the exception of promyelocytic leukemia HL-60, where TPA significantly decreased protectin cell surface expression. All-trans retinoic acid weakly down-regulated cell surface protectin on K-562, while 1,25(OH)2-vitamin D3 produced such effect on HL-60 cells. None of the examined cytokines induced a significant protectin down-regulation in the examined cell lines.
Ovarian Neoplasms, Membrane Glycoproteins, Carcinoma, Cell Membrane, Down-Regulation, Fluorescent Antibody Technique, Breast Neoplasms, CD59 Antigens, Tretinoin, Glioma, Flow Cytometry, Calcitriol, Leukemia, Promyelocytic, Acute, Antigens, CD, Leukemia, Myeloid, Cytokines, Humans, Tetradecanoylphorbol Acetate, Electrophoresis, Polyacrylamide Gel, Female
Ovarian Neoplasms, Membrane Glycoproteins, Carcinoma, Cell Membrane, Down-Regulation, Fluorescent Antibody Technique, Breast Neoplasms, CD59 Antigens, Tretinoin, Glioma, Flow Cytometry, Calcitriol, Leukemia, Promyelocytic, Acute, Antigens, CD, Leukemia, Myeloid, Cytokines, Humans, Tetradecanoylphorbol Acetate, Electrophoresis, Polyacrylamide Gel, Female
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