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Tea extract increases cell fusion via regulation of cell surface DC-STAMP

机译:茶提取物通过调节细胞表面DC-STAMP增强细胞融合

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摘要

Mononuclear osteoclast precursor cells fuse with each other to become mature multinucleated osteoclasts, which is regulated by dendritic cell-specific transmembrane protein (DC-STAMP). We evaluated the effects of tea extract and catechins on cell-cell fusion and DC-STAMP expression to elucidate their relationship with osteoclast development. When tea extract or epigallocatechin gallate (EGCg) was applied to RAW264.7 cells, multinucleated cells were increased significantly, while tartrate-resistant acid phosphatase (TRAP) activity was hardly upregulated. Flow cytometric analysis revealed that EGCg suppressed DC-STAMP expression on the cell surface, which is similar to osteoclast development. These observations suggest that TRAP activity is not activated even when suppression of both surface DC-STAMP expression and multinucleation occurs, which might be mediated by another pathway.
机译:单核破骨细胞前体细胞相互融合,形成成熟的多核破骨细胞,由树突状细胞特异性跨膜蛋白(DC-STAMP)调节。我们评估了茶提取物和儿茶素对细胞-细胞融合和DC-STAMP表达的影响,以阐明它们与破骨细胞发育的关系。当茶提取物或表没食子儿茶素没食子酸酯(EGCg)应用于RAW264.7细胞时,多核细胞显着增加,而抗酒石酸的酸性磷酸酶(TRAP)活性几乎没有上调。流式细胞仪分析表明,EGCg抑制了DC-STAMP在细胞表面的表达,这与破骨细胞的发育相似。这些观察结果表明,即使同时抑制表面DC-STAMP表达和多核化(可能由另一种途径介导),TRAP活性也不会被激活。

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