FOLLOWUS
1. Institute of Integrative Medicine, Xiangya Hospital, Central South University,Changsha,China
2. Telemedicine Centre, Xiangya Hospital, Central South University,Changsha,China
纸质出版日期:2012,
网络出版日期:2011-10-12,
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Zeng, G., Chen, J., Liang, Qh. et al. Ursolic acid inhibits T-cell activation through modulating nuclear factor-κ B signaling., Chin. J. Integr. Med. 18, 34–39 (2012). https://doi.org/10.1007/s11655-011-0858-0
Guang Zeng, Jiang Chen, Qing-hua Liang, et al. Ursolic acid inhibits T-cell activation through modulating nuclear factor-κ B signaling[J]. Chinese Journal of Integrative Medicine, 2012,18(1):34-39.
Zeng, G., Chen, J., Liang, Qh. et al. Ursolic acid inhibits T-cell activation through modulating nuclear factor-κ B signaling., Chin. J. Integr. Med. 18, 34–39 (2012). https://doi.org/10.1007/s11655-011-0858-0 DOI:
Guang Zeng, Jiang Chen, Qing-hua Liang, et al. Ursolic acid inhibits T-cell activation through modulating nuclear factor-κ B signaling[J]. Chinese Journal of Integrative Medicine, 2012,18(1):34-39. DOI: 10.1007/s11655-011-0858-0.
To investigate the effects of ursolic acid (UA) on T-cell proliferation and activation
as well as to examine its effect on nuclear factor-κB (NF-κB) signaling pathway in T cells. T-cells isolated from BALB/c mice were incubated with UA at concentrations ranging from 5–30 μmol/L in the presence of phorbol 12-myristate 13-acetate (PMA) or PMA plus ionomycin. The proliferation of T cells was measured by the MTT assay. The expressions of CD69
CD25
and CD71 on T-cell surface were analyzed using flow cytometry. The level of interleukin-2 (IL-2) in the culture supernatant of activated T cells was quantified by enzyme-linked immunosorbent assay (ELISA). The level of phosphorylated IκB-α (p-IκB-α) in total protein and p65
a subunit of NF-κB
nuclear translocation were measured by Western blot analysis. UA in a dose-dependent manner significantly decreased the proliferation and inhibited the surface expressions of CD69
CD25
and CD71 in murine T lymphocytes upon in vitro activation (P<0.01). Significant reduction of IL-2 production was found in activated T cells treated with UA (P<0.01). The PMA-induced increase in p-IκB-α protein was inhibited
and nuclear translocation of p65 from the cytoplasm was blocked by UA. UA is a potent inhibitor for T cell activation and proliferation; these effects are associated with the inhibition of NF-κB signaling pathway.
To investigate the effects of ursolic acid (UA) on T-cell proliferation and activation
as well as to examine its effect on nuclear factor-κB (NF-κB) signaling pathway in T cells. T-cells isolated from BALB/c mice were incubated with UA at concentrations ranging from 5–30 μmol/L in the presence of phorbol 12-myristate 13-acetate (PMA) or PMA plus ionomycin. The proliferation of T cells was measured by the MTT assay. The expressions of CD69
CD25
and CD71 on T-cell surface were analyzed using flow cytometry. The level of interleukin-2 (IL-2) in the culture supernatant of activated T cells was quantified by enzyme-linked immunosorbent assay (ELISA). The level of phosphorylated IκB-α (p-IκB-α) in total protein and p65
a subunit of NF-κB
nuclear translocation were measured by Western blot analysis. UA in a dose-dependent manner significantly decreased the proliferation and inhibited the surface expressions of CD69
CD25
and CD71 in murine T lymphocytes upon in vitro activation (P<0.01). Significant reduction of IL-2 production was found in activated T cells treated with UA (P<0.01). The PMA-induced increase in p-IκB-α protein was inhibited
and nuclear translocation of p65 from the cytoplasm was blocked by UA. UA is a potent inhibitor for T cell activation and proliferation; these effects are associated with the inhibition of NF-κB signaling pathway.
Ursolic AcidT-cell activationCD69CD25CD71nuclear factor-κB
Ursolic AcidT-cell activationCD69CD25CD71nuclear factor-κB
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