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The Effects of 56783′4′-Hexamethoxyflavone on Apoptosis of Cultured Human Choriocarcinoma Trophoblast Cells

机译:567834-六甲氧基黄酮对人绒毛膜滋养细胞滋养层细胞凋亡的影响

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摘要

5,6,7,8,3,4′-Hexamethoxyflavone, also called nobiletin (NOB), widely found in the citrus peel, is one of the main byproducts in citrus processing. NOB is considered safe, but its safety for women during pregnancy is unknown. Therefore, the effect of NOB on apoptosis in human choriocarcinoma trophoblast cells (BeWo cells) was evaluated. Cells were divided into four groups and cultured with different concentrations of NOB (0, 10, 33, and 100 μM) for 12, 24, 36, and 48 h respectively. Cell viability was detected by CCK-8 assay, cell morphology was detected by a Cell Imaging Multi-Mode Reader, and cell cycle and apoptosis were detected by flow cytometry. Cleaved PARP level, the expressions of B cell lymphoma 2 (BCL2) family proteins, and p53 pathway proteins were detected by Western blot. The results showed that after 48 h of cell culture, the cell viability was decreased significantly, but apoptosis was significantly increased. Compared to the cells without NOB treatment, the cells treated with NOB at 10 or 33 μΜ showed no significant differences in the number of suspended cells or late apoptosis rate, except the increase of cell viability. Treatment of NOB at the concentration of 100 μM improved cell viability, attenuated apoptosis, decreased suspended cells, and did not alter the G1 phase arrest, compared with the non-NOB-treated group after 48 h of culturing. The 100 μΜ NOB treatment increased the levels of BCL2 and BCLX , and decreased p53 accumulation in BeWo cells at 48 h, but had no effect on the expression of BAX, BAK, BAD, p21, and G1 phase arrest. These findings provide evidence that NOB (10, 33, and 100 μΜ) was safe for BeWo cells. NOB at the concentration of 100 μΜ could attenuate apoptosis in BeWo cells, which might be helpful to prevent pregnancy-related diseases caused by apoptosis.
机译:5,6,7,8,3,4'-六甲氧基黄酮,也称为nobiletin(NOB),广泛存在于柑桔皮中,是柑桔加工中的主要副产物之一。 NOB被认为是安全的,但其在孕妇中的安全性尚不清楚。因此,评估了NOB对人绒癌组织滋养细胞(BeWo细胞)凋亡的影响。将细胞分为四组,并分别用不同浓度的NOB(0、10、33和100μM)培养12、24、36和48 h。通过CCK-8测定法检测细胞存活力,通过细胞成像多模式读取器检测细胞形态,并通过流式细胞术检测细胞周期和凋亡。 Western blot检测切开的PARP水平,B细胞淋巴瘤2(BCL2)家族蛋白和p53途径蛋白的表达。结果表明,细胞培养48 h后,细胞活力明显下降,但凋亡明显增加。与未进行NOB处理的细胞相比,以10或33μM的NOB处理的细胞在悬浮细胞数或晚期凋亡率上没有显着差异,除了细胞活力增加。与未用NOB处理的组相比,在培养48小时后,以100μM的浓度处理NOB可以提高细胞活力,减少凋亡,减少悬浮细胞,并且不改变G1期停滞。 100μMNOB处理在48 h时增加了BeWo细胞中BCL2和BCLX的水平,并减少了p53的积累,但对BAX,BAK,BAD,p21和G1期停滞的表达没有影响。这些发现提供了NOB(10、33和100μM)对于BeWo细胞是安全的证据。浓度为100μM的NOB可以减弱BeWo细胞的凋亡,这可能有助于预防由凋亡引起的妊娠相关疾病。

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