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Screening Five Qi-Tonifying Herbs on M2 Phenotype Macrophages

机译:在M2表型巨噬细胞上筛选五种补气草药

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摘要

Tumor-associated macrophages (TAMs) with M2 phenotype play an essential role in tumor microenvironment (TME) during the progression and development of numerous cancers and associated with poor prognosis. Thus, regulation of TAMs polarization emerged as a new strategy for tumor immune therapy. According to Traditional Chinese Medicine (TCM) theory, herbs with Qi-tonifying character are involved in improving the defense capacity of immune system. In this study, we screened extracts and ingredients from five Qi-tonifying herbs exhibiting an inhibitory effect on M2 polarization of murine macrophages RAW264.7 induced by IL-4 and IL-13. Among these candidates, total flavonoids from Glycyrrhiza Radix et Rhizoma (TFRG) and ethanol extract of Ginseng Radix et Rhizoma significantly inhibited the expression of Arginase-1 (Arg-1) (above 90% at 100μg/mL), one of the phenotype markers of M2 macrophages. The inhibition of total saponins of Ginseng Radix et Rhizoma, ethanol extract of Cordyceps, ethanol extract of Acanthopanacis senticosi Radix et Rhizoma Seu caulis, and ethanol extract of Astragali Radix reached above 50% at 100μg/mL. The inhibition of ingredients including glabridin, isoliquiritin apioside, lysionotin, cordycepin, astragaloside IV, and calycosin reached above 50% at 50μM. Then, we investigated the molecular mechanisms of TFRG. TFRG abolished the migration of murine breast cancer 4T1 stimulated by the conditioned medium from M2 macrophages (M2-CM). In addition to Arg-1, TFRG also antagonized the IL-4/13-mediated mRNA upregulation of the M2 markers including found in inflammatory zone 1 (FIZZ1), chitinase-3-like protein 3 (YM1), and mannose receptor (CD206) and upregulated the expression of inducible nitric oxide synthase (iNOS), one of the M1 markers. The further exploration showed that TFRG decreased the phosphorylation of STAT6 and increased the expression of miR-155. Our study provides a series of potential immune regulating natural products from five Qi-tonifying herbs on M2 phenotype. For instance, TFRG suppressed M2 polarization of macrophages partly by inactivating STAT6 pathway and enhanced the level of miR-155 to regulate the expressions of M1 and M2 markers.
机译:具有M2表型的肿瘤相关巨噬细胞(TAM)在多种癌症的进展和发展过程中在肿瘤微环境(TME)中起着至关重要的作用,并且与不良预后相关。因此,调节TAMs极化已成为肿瘤免疫治疗的新策略。根据中医理论,具有补气功能的草药与提高免疫系统的防御能力有关。在这项研究中,我们筛选了五种补气中草药的提取物和成分,这些草药对IL-4和IL-13诱导的鼠巨噬细胞RAW264.7的M2极化具有抑制作用。在这些候选物中,甘草总黄酮(TFRG)和人参总黄酮的乙醇提取物显着抑制了Arginase-1(Arg-1)的表达(100μg/ mL时超过90%),这是表型标记之一M2巨噬细胞。 100μg/ mL对人参总皂苷,虫草乙醇提取物,刺五加乙醇提取物,黄芪总乙醇提取物的抑制作用均达到50%以上。 50μM时,抑制素包括加拉巴丁,异quiritritin apioside,lysionotin,虫草素,黄芪甲苷IV和calycosin的抑制率达到50%以上。然后,我们研究了TFRG的分子机制。 TFRG消除了条件培养基刺激的小鼠乳腺癌4T1从M2巨噬细胞(M2-CM)的迁移。除Arg-1外,TFRG还拮抗IL-4 / 13介导的M2标记的mRNA上调,包括在炎症区1(FIZZ1),几丁质酶-3样蛋白3(YM1)和甘露糖受体(CD206)中发现的M2标记。 )并上调了M1标记之一的诱导型一氧化氮合酶(iNOS)的表达。进一步的研究表明,TFRG降低STAT6的磷酸化并增加miR-155的表达。我们的研究提供了五种补气中草药对M2表型的一系列潜在的免疫调节天然产物。例如,TFRG通过使STAT6通路失活来部分抑制巨噬细胞的M2极化,并增强miR-155的水平以调节M1和M2标记的表达。

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