Department of Pharmacology, College of Oriental Medicine, Institute of Oriental Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Cytokine. 2011 Jun;54(3):239-43. doi: 10.1016/j.cyto.2011.03.007. Epub 2011 Apr 3.
Thymic stromal lymphopoietin (TSLP) plays a pivotal role in allergic diseases such as atopic dermatitis, asthma, and chronic obstructive pulmonary disease. Although there are many reports regarding function and regulatory mechanism of TSLP in dendritic cells and/or T cells, the regulatory mechanism of TSLP in mast cells has not been fully elucidated. Here, we describe how TSLP is expressed and produced by inflammatory stimulus in mast cells. TSLP mRNA was expressed by phorbol myristate acetate (PMA) plus A23187 stimulation in HMC-1 cells and reached its peak 5h after PMA plus A23187 stimulation. The expression of TSLP mRNA was inhibited by nuclear factor (NF)-κB inhibitor. In addition, NF-κB luciferase activity was inhibited by caspase-1 inhibitor, indicating that caspase-1 is an upstream of NF-κB in mast cells. Furthermore, caspase-1 inhibitor decreased the expression of TSLP mRNA induced by PMA plus A23187. Finally, TSLP production was inhibited by both caspase-1 inhibitor and NF-κB inhibitor. These results provide proof of principle that TSLP can be expressed and produced through caspase-1 and NF-κB in mast cells and open new perspectives to pharmacologically manipulate the expression and production of TSLP by molecules acting on the caspase-1 and NF-κB pathway.
胸腺基质淋巴细胞生成素(TSLP)在特应性皮炎、哮喘和慢性阻塞性肺疾病等过敏性疾病中发挥着关键作用。尽管有许多关于 TSLP 在树突状细胞和/或 T 细胞中的功能和调节机制的报道,但 TSLP 在肥大细胞中的调节机制尚未完全阐明。在这里,我们描述了 TSLP 如何在肥大细胞中被炎症刺激物表达和产生。在 HMC-1 细胞中,佛波醇肉豆蔻酸酯(PMA)加 A23187 刺激可表达 TSLP mRNA,刺激后 5 小时达到峰值。NF-κB 抑制剂可抑制 TSLP mRNA 的表达。此外,半胱天冬酶-1 抑制剂抑制 NF-κB 荧光素酶活性,表明半胱天冬酶-1 是肥大细胞中 NF-κB 的上游。此外,半胱天冬酶-1 抑制剂可降低 PMA 加 A23187 诱导的 TSLP mRNA 的表达。最后,半胱天冬酶-1 抑制剂和 NF-κB 抑制剂均可抑制 TSLP 的产生。这些结果为 TSLP 可以通过肥大细胞中的半胱天冬酶-1 和 NF-κB 表达和产生提供了原理证明,并为通过作用于半胱天冬酶-1 和 NF-κB 途径的分子来药理学地操纵 TSLP 的表达和产生开辟了新的视角。