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炎症微环境中乳酸驱动的巨噬细胞极化缓解肠道炎症。

Lactate-driven macrophage polarization in the inflammatory microenvironment alleviates intestinal inflammation.

机构信息

The Second Clinical Medical College, Lanzhou University, Lanzhou, China.

Department of Breast Surgery, Gansu Maternal and Child Health Care Hospital, Lanzhou, Gansu Province, China.

出版信息

Front Immunol. 2022 Oct 18;13:1013686. doi: 10.3389/fimmu.2022.1013686. eCollection 2022.

Abstract

BACKGROUND

Lactate has long been considered an intermediate by-product of glucose metabolism. However, in recent years, accumulating evidence reveals that lactate has unique biological activities. In previous studies, lactate signaling was shown to inhibit inflammation. Furthermore, experiments have shown that lactate can promote the transformation of pro-inflammatory macrophages into anti-inflammatory macrophages. However, no studies have shown whether lactate can alleviate inflammation.

METHODS

RAW 264.7 macrophages were stimulated by LPS to induce an M1 phenotype, and cultured with low and high concentrations of lactate. The cells were then observed for phenotypic transformations and expression of inflammatory mediators and surface markers. The expression of inflammatory factors was also analyzed in the cell-free supernatant fraction. Further, a mouse model of DSS-induced colitis was established and treated with lactate. Colonic tissue injury was monitored by histopathological examinations.

RESULTS

The experiments showed that lactate promoted the transformation of activated macrophages to M2 phenotype and decreased the expression of TLR4-mediated NF-κB signaling proteins and inflammatory factors. In the DSS-induced colitis mouse model, lactate promoted the phenotypic transformation of macrophages in colonic tissue, reduced inflammation and organ damage, inhibited the activation of TLR4/NF-κB signaling pathway, decreased the serum levels of pro-inflammatory factors, increased the expression of anti-inflammatory factors, promoted the repair of the intestinal mucosal barrier and reduced the severity of colitis.

CONCLUSIONS

Lactate inhibits the TLR/NF-κB signaling pathway and the production of pro-inflammatory factors by promoting polarization of macrophages. In addition, lactate promotesthe repair of the intestinal mucosal barrier and protects intestinal tissue in inflammation. Furthermore, lactate is relatively safe. Therefore, lactate is a promising and effective drug for treating inflammation through immunometabolism regulation.

摘要

背景

乳酸长期以来一直被认为是葡萄糖代谢的中间副产物。然而,近年来,越来越多的证据表明乳酸具有独特的生物学活性。在之前的研究中,乳酸信号被证明可以抑制炎症。此外,实验表明乳酸可以促进促炎巨噬细胞向抗炎巨噬细胞的转化。然而,尚无研究表明乳酸是否可以缓解炎症。

方法

用 LPS 刺激 RAW 264.7 巨噬细胞诱导 M1 表型,并用低浓度和高浓度的乳酸培养细胞。然后观察细胞表型转化和炎症介质及表面标志物的表达。还分析了细胞无血清上清部分中炎症因子的表达。此外,建立了 DSS 诱导的结肠炎小鼠模型,并使用乳酸进行治疗。通过组织病理学检查监测结肠组织损伤。

结果

实验表明,乳酸促进了激活的巨噬细胞向 M2 表型的转化,降低了 TLR4 介导的 NF-κB 信号蛋白和炎症因子的表达。在 DSS 诱导的结肠炎小鼠模型中,乳酸促进了结肠组织中巨噬细胞的表型转化,减轻了炎症和器官损伤,抑制了 TLR4/NF-κB 信号通路的激活,降低了促炎因子的血清水平,增加了抗炎因子的表达,促进了肠道黏膜屏障的修复,减轻了结肠炎的严重程度。

结论

乳酸通过促进巨噬细胞极化来抑制 TLR/NF-κB 信号通路和促炎因子的产生。此外,乳酸促进肠道黏膜屏障的修复并保护炎症中的肠道组织。而且,乳酸相对安全。因此,乳酸通过免疫代谢调节治疗炎症是一种有前途和有效的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc3a/9623299/c5b1ed67be3a/fimmu-13-1013686-g001.jpg

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