Volume 17, Issue 5 pp. 701-706
Article
Full Access

Induction of human B cell proliferation and differentiation by the combination of phorbol ester and ionomycin

Chaim M. Roifman

Corresponding Author

Chaim M. Roifman

Division of Immunology and Rheumatology, Research Institute, The Hospital for Sick Children, Toronto

Division of Immunology and Rheumatology, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G1X8, CanadaSearch for more papers by this author
Stephen H. Benedict

Stephen H. Benedict

Division of Immunology and Rheumatology, Research Institute, The Hospital for Sick Children, Toronto

Recipient of a Terry Fox fellowship award.

Search for more papers by this author
Roy K. Cheung

Roy K. Cheung

Division of Immunology and Rheumatology, Research Institute, The Hospital for Sick Children, Toronto

Search for more papers by this author
Erwin W. Gelfand

Erwin W. Gelfand

Division of Immunology and Rheumatology, Research Institute, The Hospital for Sick Children, Toronto

Search for more papers by this author
First published: 1987
Citations: 10

Abstract

Phorbol esters and Ca2+ ionophores are known to mimic intracellular messengers involved in cell activation. We studied the effects of 12-O-tetradecanoylphorbol 13-acetate (TPA) and ionomycin on tonsil and peripheral blood-derived B lymphocytes. We show that TPA and ionomycin are co-mitogenic and induce B lymphocyte differentiation. Although TPA in high concentrations is mitogenic to B lymphocytes by itself, submitogenic concentrations of TPA in combination with ionomycin trigger 50% of B lymphocytes to synthesize DNA. Stimulation of B lymphocytes with TPA plus ionomycin resulted in increased magnitude and a shift in the kinetics of c-fos and c-myc expression compared with either agent used alone. Activation markers such as the transferrin and interleukin 2 (IL 2) receptors were markedly increased after 24 h incubation with TPA and ionomycin. In parallel to the rapid proliferative burst, we observed evidence for B lymphocyte differentiation with an increase in the number of cells expressing cytoplasmic immunoglobulin (Ig) and the disappearance of the B1 surface marker. Since the cells remained surface Ig+ and secreted only small quantities of Ig, our results suggest that the combination of TPA and ionomycin is a potent inducer of B cell proliferation and early differentiation; terminal differentiation to an Ig-secreting state, however, is not achieved.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.