Secoemestrin C inhibits activation of NKT/conventional T cells and
protects against concanavalin A-induced autoimmune hepatitis in mice
Abstract
Background and Purpose: We previously found that secoemestrin C, an
epitetrathiodioxopiperazine isolated from Aspergillus nidulans, has a
potent immunosuppressive effect on splenocyte proliferation in drug
screening. Here, we determined the immunomodulatory and hepatoprotective
effects of secoemestrin C in a mouse model of acute autoimmune
hepatitis. Experimental Approach: In an in vitro assay, purified hepatic
mononuclear cells (MNCs) from C57BL/6J mice were stimulated with
concanavalin A (Con A, 2 μg·mL-1) in the presence of secoemestrin C, and
cell proliferation and cytokine production were measured. In an in vivo
assay, mice with or without secoemestrin C pretreatment were injected
with Con A (12 mg·kg-1) to induce acute hepatitis. Blood samples and
liver tissues were harvested 8 h after Con A injection. Liver injury,
serum levels of proinflammatory cytokines, hepatic lymphocyte subset
ratios, and the functional status of NKT and conventional T cells were
analyzed. Key Results: Secoemestrin C treatment dose-dependently
suppressed cell proliferation and proinflammatory cytokine secretion in
Con A-stimulated hepatic MNCs in vitro. In Con A-challenged mice,
pre-injection with secoemestrin C significantly decreased the generation
of proinflammatory cytokines and ameliorated liver injury. Furthermore,
pretreatment with secoemestrin C significantly inhibited the Con
A-induced activation of NKT and conventional T cells and decreased the
production of IFN-γ by these two cell populations. Conclusion and
Implications: Secoemestrin C has an immunosuppressive effect on NKT and
conventional T cells and has hepatoprotective activity in mouse
autoimmune hepatitis. These findings provide new insights into the use
of fungus-derived natural products for the treatment of autoimmune
diseases.