Dm. Dixon et Ml. Misfeldt, GM-CSF IS REQUIRED FOR THE PSEUDOMONAS EXOTOXIN A-INDUCED PROLIFERATION OF IMMATURE T-CELLS IN ATHYMIC MICE, Cellular immunology, 160(1), 1995, pp. 65-70
Previous studies have demonstrated that Pseudomonas exotoxin A stimula
ted the proliferation of immature T lymphocytes within the splenocytes
of athymic mice. These studies were performed to determine which lymp
hokines were involved in the proliferation of the immature T cells. Th
e results of this study indicate that exotoxin A does not induce the p
roduction of interleukin-a or tumor necrosis factor from B cell-deplet
ed splenotypes from athymic mice. However, exotoxin A does induce the
production of granulocyte-macrophage colony-stimulating factor (GM-CSF
) from B cell-depleted splenocytes. Furthermore, the GM-CSF was shown
to be produced by a Thy1(+), CD4(-), CD8(-) T lymphocyte. The addition
of anti-GM-CSF antibody abrogates the exotoxin A-induced proliferatio
n of B cell-depleted splenocytes from athymic mice. Thus, these data i
ndicate that exotoxin A induces the production of GM-CSF from immature
T lymphocytes within the splenocytes of athymic mice and the exotoxin
A-induced proliferation of these immature T cells is dependent on the
presence of GM-CSF. (C) 1995 Academic Press, Inc.