首页> 外文期刊>Japanese Journal of Cancer Research >Green tea polyphenols induce apoptosis in vitro in peripheral blood T lymphocytes of adult T-cell leukemia patients.
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Green tea polyphenols induce apoptosis in vitro in peripheral blood T lymphocytes of adult T-cell leukemia patients.

机译:绿茶多酚可在成年T细胞白血病患者的外周血T淋巴细胞中诱导细胞凋亡。

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Green tea polyphenols (TEA) are known to exhibit antioxidative activity as well as tumor-suppressing activity. In order to examine the tumor-suppressing activity of TEA against adult T-cell leukemia (ATL), we cultivated peripheral blood T lymphocytes of ATL patients (ATL PBLs), an HTLV-I-infected T-cell line (KODV) and healthy controls (normal PBLs) for 3 days in the presence of TEA and its main constituent, epigallocatechin-3-gallate (EGCg), to measure cell proliferation and apoptosis, and to quantitate mRNAs of HTLV-I pX and beta-actin genes of the cultured cells. Growth of ATL PBLs was significantly inhibited by 9-27 microg/ml of TEA and EGCg, in contrast to minimal growth inhibition of T cells of normal PBLs. Inhibition of KODV was intermediate between ATL PBLs and normal PBLs. The ATL PBLs and KODV treated with 27 microg/ml of either TEA or EGCg induced apoptotic DNA fragmentation, producing terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL)-positive cells, while the normal PBLs treated with the same concentration of TEA or EGCg produced a negligibly small number of TUNEL-positive cells, in which apoptotic DNA fragmentation was not detectable. Expression of HTLV-I pX mRNA was suppressed more than 90% in ATL PBLs by treatment with 3-27 microg/ml of either TEA or EGCg, while expression of beta-actin mRNA was much less suppressed by treatment with the same concentration of TEA or EGCg. These results indicate that TEA and EGCg inhibit growth of ATL PBLs, as well as HTLV-I-infected T-cells, by suppressing HTLV-I pX gene expression and inducing apoptotic cell death.
机译:已知绿茶多酚(TEA)具有抗氧化活性和抑瘤活性。为了检查TEA对成人T细胞白血病(ATL)的抑瘤活性,我们培养了ATL患者的外周血T淋巴细胞(ATL PBLs),HTLV-I感染的T细胞系(KODV)对照(正常PBL)在TEA及其主要成分epigallocatechin-3-gallate(EGCg)存在下进行3天,以测量细胞增殖和凋亡,并定量HTLV-1 pX和β-actin基因的mRNA。培养的细胞。 9-27微克/毫升的TEA和EGCg显着抑制了ATL PBL的生长,与正常PBL的T细胞的最小生长抑制相反。 KODV的抑制作用介于ATL PBL和正常PBL之间。用27微克/毫升TEA或EGCg处理的ATL PBL和KODV诱导凋亡的DNA片段化,产生末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记(TUNEL)阳性细胞,而正常PBL用相同浓度的TEA或EGCg产生的TUNEL阳性细胞数量很少,可以检测不到凋亡的DNA片段化。通过使用3-27 microg / ml的TEA或EGCg处理,在ATL PBL中HTLV-1 pX mRNA的表达被抑制了90%以上,而在相同浓度的TEA处理下,β-actinmRNA的表达被抑制得更少。或EGCg。这些结果表明,TEA和EGCg通过抑制HTLV-1 pX基因表达并诱导凋亡细胞死亡来抑制ATL PBLs以及HTLV-1感染的T细胞的生长。

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