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Research Article Free access | 10.1172/JCI109800

12-O-Tetradecanoyl-Phorbol-13-Acetate Release of Glycosyltransferases from Human Blood Cells

Chen-Kao Liu, Robert Schmied, and Samuel Waxman

Cancer Chemotherapy Foundation Laboratory, Mount Sinai School of Medicine, New York 10029

Division of Medical Oncology, Department of Medicine and Biochemistry, Mount Sinai School of Medicine, New York 10029

Find articles by Liu, C. in: PubMed | Google Scholar

Cancer Chemotherapy Foundation Laboratory, Mount Sinai School of Medicine, New York 10029

Division of Medical Oncology, Department of Medicine and Biochemistry, Mount Sinai School of Medicine, New York 10029

Find articles by Schmied, R. in: PubMed | Google Scholar

Cancer Chemotherapy Foundation Laboratory, Mount Sinai School of Medicine, New York 10029

Division of Medical Oncology, Department of Medicine and Biochemistry, Mount Sinai School of Medicine, New York 10029

Find articles by Waxman, S. in: PubMed | Google Scholar

Published June 1, 1980 - More info

Published in Volume 65, Issue 6 on June 1, 1980
J Clin Invest. 1980;65(6):1365–1371. https://doi.org/10.1172/JCI109800.
© 1980 The American Society for Clinical Investigation
Published June 1, 1980 - Version history
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Abstract

The mononuclear cells separated from human blood by Ficoll-Hypaque centrifugation contained and released sialyltransferase, galactosyltransferase, and fucosyltransferase. Granulocytes contained and released lesser amounts of glycosyltransferases, whereas platelets released more fucosyltransferase than sialyltransferase or galactosyltransferase. When mononuclear cells were incubated with 12-O-tetradecanoyl-phorbol-13-acetate (TPA), the release of these three glycosyltransferases increased two- to six-fold, and cell suspension glycosyltransferase activities decreased 10-50%. Mononuclear cells were fractionated into lymphocytes and monocytes using baby hamster kidney cells microexudate-coated flasks. TPA stimulated the release of glycosyltransferases from lymphocytes but not from monocytes. The release of glycosyltransferases by TPA-treated mononuclear cells was not further stimulated by reincubation with TPA and was not affected by puromycin, cAMP, or cGMP. Concanavalin A, a mitogenic stimulator of lymphocytes, also stimulated the release of glycosyltransferases from mononuclear cells, but to a lesser extent. TPA did not stimulate the release of 5′-nucleotidase or decrease its activity on the cell pellet. Triton X-100 (0.2%) stimulated the release of glycosyltransferases to the same extent as TPA, but also caused the release of 5′-nucleotidase. [3H]TPA bound specifically and reversibly to mononuclear cells. The possible relationship between glycosyltransferase release and TPA effect on the plasma membrane is discussed.

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