Abstract
We have shown that pertussis toxin (PTx) modulates the effect of tumor necrosis factor-alpha (TNF-α) in inducing monocytic differentiation of WEHI-3B (JCS) myeloid leukemic cells in vitro. PTx (0.1–2 ng/ml) alone was not cytotoxic and did not induce morphological changes in JCS cells. In the presence of a suboptimal concentration of TNF-α (25 U/ml), however, PTx (1 ng/ml) acted synergistically in inhibiting proliferation and in inducing monocytic differentiation of the JCS cells. Expression of the macrophage differentiation marker (Mac-1) on JCS cells was increased by the combination of PTx and TNF-α, and phagocytic activity of the cells was also enhanced. Moreover, JCS cells treated with PTx and TNF-α had reduced tumorigenic capacity in vivo. The data suggest that a PTx-sensitive G protein may be involved in regulating the TNF-α-induced monocytic differentiation of the myeloid leukemic JCS cells and that combination of PTx and TNF-α may be useful in the treatment of some forms of myelomonocytic leukemia.
Original language | English |
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Pages (from-to) | 1-12 |
Number of pages | 12 |
Journal | Immunobiology |
Volume | 190 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 1994 |
Scopus Subject Areas
- Immunology and Allergy
- Immunology
- Hematology
User-Defined Keywords
- G protein
- guanine-nucleotide-binding protein
- mean survival time
- MST
- PBS
- pertussis toxin
- phosphate-buffered saline
- PTx
- TNF-α
- tumor necrosis factor-alpha