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作为奶牛亚急性瘤胃酸中毒反应的一部分,核因子κB参与脂多糖介导的MAC-T上皮细胞增殖和凋亡。

NF-κB is involved in the LPS-mediated proliferation and apoptosis of MAC-T epithelial cells as part of the subacute ruminal acidosis response in cows.

作者信息

Fan Wen-Jie, Li He-Ping, Zhu He-Shui, Sui Shi-Ping, Chen Pei-Ge, Deng Yue, Sui Tong-Ming, Wang Yue-Ying

机构信息

Key Laboratory of Animal Biochemistry and Nutrition, Ministry of Agriculture, Henan Agricultural University, Zhengzhou, Henan, China.

College of Animal Husbandary and Verterinary Science, Henan Agricultural University, Wenhua Road 95, Zhengzhou, 450002, China.

出版信息

Biotechnol Lett. 2016 Nov;38(11):1839-1849. doi: 10.1007/s10529-016-2178-0. Epub 2016 Jul 22.

Abstract

OBJECTIVES

To determine the effect of NF-κB on cell proliferation and apoptosis, we investigate the expression of inflammation and apoptosis-related factors in the bovine mammary epithelial cell line, MAC-T.

RESULTS

MAC-T cells were cultured in vitro and MTT and LDH assays used to determine the effects of lipopolysaccharide (LPS) on proliferation and cytotoxicity respectively. RT-PCR and western blotting were used to evaluate the effect of LPS and NF-κB inhibition [pyrrolidine dithiocarbamate (PDTC) treatment] on the expression of inflammation and apoptosis-related factors. LPS significantly inhibited MAC-T cell proliferation in a dose- and time-dependent manner. Furthermore, LPS promoted apoptosis while the NF-кB inhibitor PDTC attenuated this effect. After LPS treatment, the NF-кB signaling pathway was activated, and the expression of inflammation and apoptosis-related factors increased. When PDTC blocked NF-кB signaling, the expression of inflammation and apoptosis-related factors were decreased in MAC-T cells.

CONCLUSIONS

LPS activates the TLR4/NF-κB signaling pathway, inhibits proliferation and promotes apoptosis in MAC-T cells. NF-кB inhibition attenuates MAC-T cell apoptosis and TLR4/NF-κB signaling pathway. NF-кB inhibitor alleviating MAC-T cell apoptosis is presumably modulated by NF-кB.

摘要

目的

为了确定核因子κB(NF-κB)对细胞增殖和凋亡的影响,我们研究了牛乳腺上皮细胞系MAC-T中炎症和凋亡相关因子的表达。

结果

体外培养MAC-T细胞,分别采用MTT法和LDH法检测脂多糖(LPS)对细胞增殖和细胞毒性的影响。采用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法评估LPS和NF-κB抑制(吡咯烷二硫代氨基甲酸盐(PDTC)处理)对炎症和凋亡相关因子表达的影响。LPS以剂量和时间依赖性方式显著抑制MAC-T细胞增殖。此外,LPS促进细胞凋亡,而NF-κB抑制剂PDTC减弱了这种作用。LPS处理后,NF-κB信号通路被激活,炎症和凋亡相关因子的表达增加。当PDTC阻断NF-κB信号时,MAC-T细胞中炎症和凋亡相关因子的表达降低。

结论

LPS激活TLR4/NF-κB信号通路,抑制MAC-T细胞增殖并促进其凋亡。抑制NF-κB可减轻MAC-T细胞凋亡并阻断TLR4/NF-κB信号通路。NF-κB抑制剂减轻MAC-T细胞凋亡可能是由NF-κB介导的。

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