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黄芩中的黄酮类化合物通过阻断 Toll 样受体 4/髓样分化因子 88/核因子-κB 信号通路抑制肿瘤相关巨噬细胞的激活。

Flavonoids from Scutellaria barbata inhibit activation of tumor-associated macrophages by blocking the Toll-like receptor 4/myeloid differentiation factor 88/nuclear factor-κB signaling pathway.

机构信息

Department of Gynecology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.

出版信息

J Tradit Chin Med. 2019 Apr;39(2):160-165.

Abstract

OBJECTIVE

To determine the efficacy of Scutellaria barbata flavonoids and polysaccharides on Ishikawa endometrial carcinoma cells co-cultured with U937 macrophages.

METHODS

The presence of CD163 and CD206 was determined by flow cytometry. Thiazolyl Blue Tetrazolium Bromide assays were used to assess the proliferation effect of tumor-associated macrophages (TAMs) on Ishikawa cells. The secretion of interleukin (IL)-10 in the co-culture conditioned media was examined using an enzyme-linked immunosorbent assay. The protein expression levels of Toll-like receptor 4 (TLR4), myeloid differentiation factor 88 (MyD88) and nuclear factor (NF)-κB p65 were detected by Western blot. The mRNA expression levels of TLR4 and MyD88 were analyzed by real-time polymerase chain reaction (PCR). The expression levels of IL-12, IL-1β and tumor necrosis factor-α (TNF-α) were evaluated with real-time PCR.

RESULTS

Compared with the U937 control group, the expression levels of CD163 and CD206 in the TAM group were higher (P < 0.05). TAMs co-cultured with Ishikawa cells for 24 or 48 h showed higher proliferation rates (P < 0.05). The expression levels of IL-12 decreased than compared with those in the U937 untreated group (P < 0.05) and those of the Scutellaria barbata flavonoids group (P < 0.05). The expression levels of CD206, CD163, IL-10, IL-1β and TNF-α, NF-κB p65 and TLR4/MyD88 in the TAMs control group were greater than those in the U937 untreated group (P < 0.05) and those of the Scutellaria barbata flavonoids group (P < 0.05).

CONCLUSION

Scutellaria barbata flavonoids may inhibit TAM activation by blocking the TLR4/MyD88/NF-κB signaling pathway.

摘要

目的

观察白花蛇舌草总黄酮和多糖对与 U937 巨噬细胞共培养的 Ishikawa 子宫内膜癌细胞的作用。

方法

采用流式细胞术检测 CD163 和 CD206 的表达。噻唑蓝比色法检测肿瘤相关巨噬细胞(TAMs)对 Ishikawa 细胞的增殖作用。酶联免疫吸附试验检测共培养条件培养基中白细胞介素(IL)-10 的分泌。Western blot 检测 Toll 样受体 4(TLR4)、髓样分化因子 88(MyD88)和核因子(NF)-κB p65 的蛋白表达水平。实时聚合酶链反应(PCR)分析 TLR4 和 MyD88 的 mRNA 表达水平。实时 PCR 检测 IL-12、IL-1β 和肿瘤坏死因子-α(TNF-α)的表达水平。

结果

与 U937 对照组相比,TAM 组的 CD163 和 CD206 表达水平更高(P < 0.05)。与未处理的 U937 组相比,共培养 24 或 48 h 的 TAMs 增殖率更高(P < 0.05)。与未处理的 U937 组相比,白花蛇舌草总黄酮组的 IL-12 表达水平降低(P < 0.05)。TAMs 对照组的 CD206、CD163、IL-10、IL-1β 和 TNF-α、NF-κB p65 和 TLR4/MyD88 的表达水平均高于未处理的 U937 组(P < 0.05)和白花蛇舌草总黄酮组(P < 0.05)。

结论

白花蛇舌草总黄酮可能通过阻断 TLR4/MyD88/NF-κB 信号通路抑制 TAM 激活。

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