State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.
Laboratory of Cell Signaling and Modeling Genetics, Institute of Molecular Pathology, Department of Basic Medical Sciences, School of Medicine, Zhejiang University, Hangzhou, China.
J Invest Dermatol. 2014 Nov;134(11):2737-2746. doi: 10.1038/jid.2014.252. Epub 2014 Jun 16.
Increasing numbers of people are suffering from allergic contact dermatitis. However, the immunosuppressive drug candidate with negligible toxicity is still deficient. In the present study, we identified a natural cyclodepsipeptide named trichomide A that effectively inhibited the proliferation of activated T cells and reduced the production of proinflammatory cytokines but had almost no toxic effect on naive T cells at 0.3-3 μM. In addition, trichomide A caused G0/G1 phase arrest, suppressed the activation of AKT and STAT3, and increased the level of phosphorylated SHP2 in activated T cells in dose- and time-dependent manners. Furthermore, an in vivo experiment demonstrated that trichomide A significantly ameliorated picryl chloride (PCI)-induced contact hypersensitivity in mice. Such effects of trichomide A in the aforementioned experiments were significantly reversed by the inhibition of SHP2 activity using the SHP2-specific inhibitor PHPS1 or conditional SHP2 knockout mice in T cells, suggesting the SHP2-dependent action of trichomide A. Taken together, trichomide A showed an immunosuppressive activity against T cell-mediated immune responses both in vitro and in vivo, which has potential for the treatment of immune-related skin diseases.
越来越多的人患有过敏性接触性皮炎。然而,具有可忽略毒性的免疫抑制候选药物仍然缺乏。在本研究中,我们鉴定出一种天然环二肽,名为 trichomide A,它在 0.3-3 μM 时有效抑制活化 T 细胞的增殖,减少促炎细胞因子的产生,但对幼稚 T 细胞几乎没有毒性作用。此外,trichomide A 引起 G0/G1 期阻滞,抑制 AKT 和 STAT3 的激活,并在剂量和时间依赖性方式下增加活化 T 细胞中磷酸化 SHP2 的水平。此外,体内实验表明 trichomide A 显著改善了对小鼠的二硝基氯苯(PCI)诱导的接触超敏反应。在上述实验中,trichomide A 的这种作用通过使用 SHP2 特异性抑制剂 PHPS1 或 T 细胞中条件性 SHP2 敲除小鼠抑制 SHP2 活性被显著逆转,表明 trichomide A 的 SHP2 依赖性作用。总之,trichomide A 在体外和体内均显示出对 T 细胞介导的免疫反应的免疫抑制活性,具有治疗免疫相关皮肤病的潜力。