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8-甲氧基补骨脂素通过抑制 JAK/STAT 和 NF-κB 通路保护牛乳腺上皮细胞免受脂多糖诱导的炎症损伤。

8-Methoxypsoralen protects bovine mammary epithelial cells against lipopolysaccharide-induced inflammatory injury via suppressing JAK/STAT and NF-κB pathway.

机构信息

College of Animal Science and Technology, Beijing University of Agriculture, Beijing, China.

College of Veterinary Medicine, China Agricultural University, Beijing, China.

出版信息

Microbiol Immunol. 2019 Oct;63(10):427-437. doi: 10.1111/1348-0421.12730. Epub 2019 Aug 23.

DOI:10.1111/1348-0421.12730
PMID:31313848
Abstract

Bovine mastitis is the most common disease in dairy cattle. Bacterial infections are the main cause of mastitis. Lipopolysaccharide (LPS), a major structural component of the cell wall of Escherichia coli, is a good inducer used to replicate inflammation models. 8-Methoxypsoralen (8-MOP), a formerly considered photosensitizing agent, has been used in immunotherapy. This study investigated the protective effects of 8-MOP on LPS-induced inflammatory injury in bovine mammary epithelial cells (BMECs). LPS treatment (50 μg/mL for 12 hr) caused a decrease in cell viability, morphological damage, and cell apoptosis. Pretreatment with 8-MOP at concentrations of 25 and 50 μg/ml significantly attenuated LPS-induced inflammation in BMECs. qRT-PCR analysis revealed that the messenger RNA expression of inflammatory cytokines and chemokine (interleukin-1β [IL-1β], IL-6, tumor necrosis factor-α, and IL-8) was suppressed by 8-MOP in LPS-stimulated BMECs. Western blot analysis showed that 8-MOP could also reduce the protein levels of cyclooxygenase-2 and promote the translocation of high-mobility group box 1 from the nucleus to cytoplasm. Furthermore, the anti-inflammatory property of 8-MOP was mediated by inhibiting nuclear factor kappa-light-chain-enhancer of activated B cells activation and STAT1 phosphorylation. Taken together, 8-MOP could protect cells from inflammatory injury induced by LPS, and may be a potential agent against bovine mastitis.

摘要

奶牛乳腺炎是奶牛中最常见的疾病。细菌感染是乳腺炎的主要原因。脂多糖(LPS)是大肠杆菌细胞壁的主要结构成分,是一种很好的诱导剂,用于复制炎症模型。8-甲氧基补骨脂素(8-MOP)曾被认为是光敏剂,已被用于免疫治疗。本研究探讨了 8-MOP 对 LPS 诱导的奶牛乳腺上皮细胞(BMEC)炎症损伤的保护作用。LPS 处理(50μg/ml,12 小时)导致细胞活力下降、形态损伤和细胞凋亡。25 和 50μg/ml 的 8-MOP 预处理显著减轻了 LPS 诱导的 BMEC 炎症。qRT-PCR 分析显示,8-MOP 抑制了 LPS 刺激的 BMEC 中炎症细胞因子和趋化因子(白细胞介素-1β[IL-1β]、IL-6、肿瘤坏死因子-α和 IL-8)的信使 RNA 表达。Western blot 分析表明,8-MOP 还可以降低环氧化酶-2 的蛋白水平,并促进高迁移率族蛋白 1 从核内易位到细胞质。此外,8-MOP 的抗炎作用是通过抑制核因子κB 轻链增强子的激活 B 细胞和 STAT1 磷酸化来介导的。总之,8-MOP 可以保护细胞免受 LPS 诱导的炎症损伤,可能是一种防治奶牛乳腺炎的潜在药物。

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