Department of Respiratory Medicine, Jinling Hospital, Southern Medical University, Nanjing, PR China.
Department of Respiratory Medicine, Jiangning Hospital, Nanjing, PR China.
J Surg Res. 2019 Mar;235:83-92. doi: 10.1016/j.jss.2018.08.057. Epub 2018 Oct 24.
The topoisomerase 1 (Top1) inhibitor has been reported to inhibit inflammatory genes induced by virus and protect mice from sepsis. Its role in acute lung injury (ALI) remains unknown. This study aimed to explore the effects of topotecan (TPT), a Top 1 inhibitor, in lipopolysaccharide (LPS)-ALI.
THP-1 cells were stimulated with LPS and then treated with or without TPT. Inflammatory cytokines expression was measured by ELISA. In vivo, we also detected the effect of TPT in LPS-induced ALI mouse model through hematoxylin-eosin staining of lung tissue and the quantification of total protein, total cell count, and cytokines in bronchoalveolar lavage fluid. To investigate the effect of TPT on transcriptome levels, microarray analyses were performed. KEGG analysis was applied to determine potential pathways modified by TPT. Microarray results were confirmed by real-time PCR and Western blot.
TPT significantly decreased the expression of TNF-α and IL-1β induced by LPS in THP-1 cells. In an LPS-induced ALI mouse model, TPT significantly attenuated lung injury and decreased the levels of total protein, total cell count, and inflammatory cytokine expression in bronchoalveolar lavage fluid. Microarray results showed that TPT significantly increased expression of 958 genes and decreased expression of 1400 genes in THP-1 cells upon LPS stimulation. KEGG analysis demonstrated that differentially expressed genes function in multiple signaling pathways, including the nuclear factor (NF)-κB signaling pathway. The downstream gene of NF-κB, including c-IAP1/2, c-FLIP, Bcl-2, IL-8, and VCAM-1, and the phosphorylation of NF-κB p105, p65, and IκB-α were significantly decreased after TPT administration in THP-1 cells.
In conclusion, TPT attenuates LPS-induced ALI through inhibiting the NF-κB signaling pathway, suggesting that TPT might serve as a useful therapeutic for ALI. Thus, our study has provided new insight for current ALI treatment.
拓扑异构酶 1(Top1)抑制剂已被报道可抑制病毒诱导的炎症基因,并保护小鼠免受败血症的影响。但其在急性肺损伤(ALI)中的作用尚不清楚。本研究旨在探讨拓扑替康(TPT),一种 Top1 抑制剂,在脂多糖(LPS)-ALI 中的作用。
用 LPS 刺激 THP-1 细胞,然后用或不用 TPT 处理。通过 ELISA 测定炎症细胞因子的表达。在体内,我们还通过肺组织苏木精-伊红染色和支气管肺泡灌洗液中总蛋白、总细胞计数和细胞因子的定量检测,研究了 TPT 在 LPS 诱导的 ALI 小鼠模型中的作用。为了研究 TPT 对转录组水平的影响,进行了微阵列分析。KEGG 分析用于确定 TPT 修饰的潜在途径。微阵列结果通过实时 PCR 和 Western blot 进行验证。
TPT 显著降低了 LPS 诱导的 THP-1 细胞中 TNF-α和 IL-1β的表达。在 LPS 诱导的 ALI 小鼠模型中,TPT 显著减轻了肺损伤,并降低了支气管肺泡灌洗液中总蛋白、总细胞计数和炎症细胞因子表达水平。微阵列结果显示,TPT 显著增加了 LPS 刺激 THP-1 细胞中 958 个基因的表达,降低了 1400 个基因的表达。KEGG 分析表明,差异表达基因在多个信号通路中发挥作用,包括核因子(NF)-κB 信号通路。TPT 给药后,THP-1 细胞中 NF-κB 的下游基因,包括 c-IAP1/2、c-FLIP、Bcl-2、IL-8 和 VCAM-1,以及 NF-κB p105、p65 和 IκB-α的磷酸化均显著降低。
总之,TPT 通过抑制 NF-κB 信号通路减轻 LPS 诱导的 ALI,提示 TPT 可能作为一种治疗 ALI 的有用药物。因此,我们的研究为当前的 ALI 治疗提供了新的思路。