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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.

Identifieur interne : 000248 ( Main/Exploration ); précédent : 000247; suivant : 000249

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.

Auteurs : Xiaoxia Bao [République populaire de Chine] ; Liuye Li [République populaire de Chine] ; Xiaoou Xue [République populaire de Chine]

Source :

RBID : pubmed:32186037

Descripteurs français

English descriptors

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.


PubMed: 32186037


Affiliations:


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Le document en format XML

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<term>Cell Line, Tumor (MeSH)</term>
<term>Cell Proliferation (drug effects)</term>
<term>Flavonoids (pharmacology)</term>
<term>Humans (MeSH)</term>
<term>Macrophages (cytology)</term>
<term>Macrophages (drug effects)</term>
<term>Macrophages (metabolism)</term>
<term>Myeloid Differentiation Factor 88 (metabolism)</term>
<term>NF-kappa B (metabolism)</term>
<term>Scutellaria (chemistry)</term>
<term>Signal Transduction (drug effects)</term>
<term>Toll-Like Receptor 4 (metabolism)</term>
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<term>Facteur de différenciation myéloïde-88 (métabolisme)</term>
<term>Facteur de transcription NF-kappa B (métabolisme)</term>
<term>Flavonoïdes (pharmacologie)</term>
<term>Humains (MeSH)</term>
<term>Lignée cellulaire tumorale (MeSH)</term>
<term>Macrophages (cytologie)</term>
<term>Macrophages (effets des médicaments et des substances chimiques)</term>
<term>Macrophages (métabolisme)</term>
<term>Prolifération cellulaire (effets des médicaments et des substances chimiques)</term>
<term>Récepteur de type Toll-4 (métabolisme)</term>
<term>Scutellaria (composition chimique)</term>
<term>Transduction du signal (effets des médicaments et des substances chimiques)</term>
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<term>NF-kappa B</term>
<term>Toll-Like Receptor 4</term>
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<term>Scutellaria</term>
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<term>Scutellaria</term>
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<term>Macrophages</term>
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<term>Macrophages</term>
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<term>Macrophages</term>
<term>Signal Transduction</term>
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<term>Prolifération cellulaire</term>
<term>Transduction du signal</term>
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<term>Macrophages</term>
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<term>Facteur de différenciation myéloïde-88</term>
<term>Facteur de transcription NF-kappa B</term>
<term>Macrophages</term>
<term>Récepteur de type Toll-4</term>
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<b>OBJECTIVE</b>
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<p>To determine the efficacy of Scutellaria barbata flavonoids and polysaccharides on Ishikawa endometrial carcinoma cells co-cultured with U937 macrophages.</p>
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<b>METHODS</b>
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<p>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.</p>
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<b>RESULTS</b>
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<p>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).</p>
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<b>CONCLUSION</b>
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<p>Scutellaria barbata flavonoids may inhibit TAM activation by blocking the TLR4/MyD88/NF-κB signaling pathway.</p>
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