TY - JOUR
T1 - Regulation of IL-2 production in Jurkat cells by Dictyostelium-derived factors
AU - Takahashi, Katsunori
AU - Murakami, Masami
AU - Hosaka, Kohei
AU - Kikuchi, Haruhisa
AU - Oshima, Yoshiteru
AU - Kubohara, Yuzuru
N1 - Funding Information:
The authors thank Ms. K. Nakata and Ms. Y. Hasegawa for their technical assistance. This work was supported in part by a Grant-in-aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan to M.M., Y.O., and Y.K.
PY - 2009/9/9
Y1 - 2009/9/9
N2 - Aims: Differentiation-inducing factors (DIFs) are chlorinated alkylphenones found in the cellular slime mold Dictyostelium discoideum. DIF derivatives exhibit antiproliferative activities and promote glucose consumption in mammalian cells in vitro. In this study, we assessed the ability of DIFs to regulate the immune system and investigated their mechanisms of action. Main methods: We examined the effects of 30 DIF derivatives on concanavalin A-induced IL-2 production (CIIP) in Jurkat T-cells. We also examined the effects of some DIF derivatives on the activity of AP-1 (activator protein-1), NFAT (nuclear factor of activated T-cells), and NFκB (nuclear factor kappa B), which are transcription factors required for CIIP. Key findings: Of the derivatives tested, some compounds suppressed CIIP as well as the known immunosuppressants cyclosporine A and FK506. A reporter gene assay revealed that 4 DIF derivatives tested suppressed CIIP, at least in part, by inhibiting the activity of AP-1, NFAT, and/or NFκB. Unlike cyclosporine A and FK506, the DIF derivatives had little effect on concanavalin A-induced interferon-γ production in Jurkat cells. Significance: The present results suggest that DIF derivatives could be developed as novel immunosuppressive drugs.
AB - Aims: Differentiation-inducing factors (DIFs) are chlorinated alkylphenones found in the cellular slime mold Dictyostelium discoideum. DIF derivatives exhibit antiproliferative activities and promote glucose consumption in mammalian cells in vitro. In this study, we assessed the ability of DIFs to regulate the immune system and investigated their mechanisms of action. Main methods: We examined the effects of 30 DIF derivatives on concanavalin A-induced IL-2 production (CIIP) in Jurkat T-cells. We also examined the effects of some DIF derivatives on the activity of AP-1 (activator protein-1), NFAT (nuclear factor of activated T-cells), and NFκB (nuclear factor kappa B), which are transcription factors required for CIIP. Key findings: Of the derivatives tested, some compounds suppressed CIIP as well as the known immunosuppressants cyclosporine A and FK506. A reporter gene assay revealed that 4 DIF derivatives tested suppressed CIIP, at least in part, by inhibiting the activity of AP-1, NFAT, and/or NFκB. Unlike cyclosporine A and FK506, the DIF derivatives had little effect on concanavalin A-induced interferon-γ production in Jurkat cells. Significance: The present results suggest that DIF derivatives could be developed as novel immunosuppressive drugs.
KW - DIF
KW - Dictyostelium
KW - Differentiation-inducing factor
KW - Immunosuppressive drug
KW - Interferon-γ
KW - Interleukin-2
KW - Jurkat cells
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U2 - 10.1016/j.lfs.2009.07.008
DO - 10.1016/j.lfs.2009.07.008
M3 - Article
C2 - 19632244
AN - SCOPUS:69349105301
SN - 0024-3205
VL - 85
SP - 438
EP - 443
JO - Life Sciences
JF - Life Sciences
IS - 11-12
ER -