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FK3453 抑制胸腺基质淋巴细胞生成素的产生。

Inhibition of thymic stromal lymphopoietin production by FK3453.

机构信息

Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Miyagi, Japan.

Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Miyagi, Japan.

出版信息

J Pharmacol Sci. 2022 Aug;149(4):198-204. doi: 10.1016/j.jphs.2022.05.005. Epub 2022 May 21.

Abstract

To prevent the onset and aggravation of allergic diseases, it is necessary to modulate excessive Th2-type immune responses. It is well accepted that thymic stromal lymphopoietin (TSLP) plays important roles in the change of Th1/Th2 balance to Th2 dominance and would be a druggable target. In this study, using a drug repositioning strategy, we identified 6-(2-amino-4-phenylpyrimidine-5-yl)-2-isopropylpyridazin-3(2H)-one (FK3453) as a novel inhibitor of TSLP production. FK3453 inhibited constitutive production of TSLP in the KCMH-1 mouse keratinocyte cell line and 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced one in PAM212 cells. FK3453 also inhibited TSLP mRNA expression induced by a mixture of tumor necrosis factor alpha (TNF-α), interleukin (IL)-4, fibroblast-stimulation lipopeptide-1, and protease activated-receptor agonist and TPA in normal human epidermal keratinocytes (NHEKs). Although FK3453 inhibited TPA-induced IL-33 expression in NHEKs in addition to TSLP, it did not inhibit TNF-α and IL-6 production. In addition, FK3453 did not inhibit MAP kinase (ERK) phosphorylation. We have confirmed that topical treatment with FK3453 inhibited TSLP production in the lipopolysaccharide-induced air pouch-type inflammation model. FK3453 could be a lead compound for a novel type of medicine which prevents the onset and aggravation of allergic diseases.

摘要

为了预防过敏疾病的发生和加重,有必要调节过度的 Th2 型免疫反应。人们普遍认为胸腺基质淋巴细胞生成素 (TSLP) 在 Th1/Th2 平衡向 Th2 优势的转变中起着重要作用,并且可能成为一个可成药的靶点。在这项研究中,我们使用药物再定位策略,确定了 6-(2-氨基-4-苯基嘧啶-5-基)-2-异丙基哒嗪-3(2H)-酮 (FK3453) 是 TSLP 产生的新型抑制剂。FK3453 抑制 KCMH-1 小鼠角质形成细胞系中的 TSLP 组成型产生和 PAM212 细胞中的 12-O-十四烷酰佛波醇-13-乙酸酯 (TPA) 诱导的 TSLP。FK3453 还抑制 TNF-α、IL-4、成纤维细胞刺激脂肽-1 和蛋白酶激活受体激动剂和 TPA 混合物诱导的正常人类表皮角质形成细胞 (NHEKs) 中的 TSLP mRNA 表达。尽管 FK3453 除了 TSLP 之外,还抑制了 TPA 诱导的 NHEKs 中的 IL-33 表达,但它没有抑制 TNF-α 和 IL-6 的产生。此外,FK3453 不抑制 MAP 激酶 (ERK) 磷酸化。我们已经证实,FK3453 的局部治疗抑制了脂多糖诱导的气囊型炎症模型中的 TSLP 产生。FK3453 可能成为预防过敏疾病发生和加重的新型药物的先导化合物。

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