首页|mdv1-miR-M4-5p对MDCC-MSB1细胞增殖和凋亡的影响

mdv1-miR-M4-5p对MDCC-MSB1细胞增殖和凋亡的影响

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旨在研究马立克病病毒(Marek's disease virus,MDV)编码的mdv1-miR-M4-5p对MDCC-MSB1细胞增殖和凋亡的影响,将mdv1-miR-M4-5p模拟物、抑制物及其阴性对照转染MDCC-MSB1细胞后48 h,采用实时荧光定量 PCR(qRT-PCR)检测细胞中 mdv1-miR-M4-5p、TGF-β1、Smad2以及 caspase-9、caspase-3、cyt-c、cyclinD1、Bcl-2等增殖和凋亡相关分子的转录;CCK-8检测细胞增殖,流式细胞术检测细胞周期和凋亡.结果显示:与对照组相比,mdv1-miR-M4-5p模拟物转染显著上调MDCC-MSB1细胞中mdv1-miR-M4-5p、cyclinD1、Bcl-2的转录水平,下调TGF-β1、Smad2、cyt-c、caspase-9和caspase-3的转录,促进细胞的增殖,减少G1期细胞,增加S和G2细胞,降低细胞凋亡率.与对照组相比,mdv1-miR-M4-5p抑制物转染后MDCC-MSB1细胞的增殖、凋亡及其相关分子转录的结果与mdv1-miR-M4-5p模拟物转染后的结果相反.综上,Mdv1-miR-M4-5p可促进MDCC-MSB1细胞增殖,抑制其凋亡,这可能是通过抑制TGF-β1/Smad2信号通路来实现的.
Effects of mdv1-miR-M4-5p Encoded by MDV on Proliferation and Apoptosis of MDCC-MSB1 Cells
The purpose of this experiment was to study the effects of mdv1-miR-M4-5p encoded by Marek's disease virus(MDV)on proliferation and apoptosis of MDCC-MSB1 cells.In this study,mdv1-miR-M4-5p mimics,inhibitors and their negative controls were transfected into MSB1 cells for 48 h.Real-time quantitative fluorescent PCR(qRT-PCR)was used to detect the transcription of mdv1-miR-M4-5p,TGF-β1,Smad2,caspase-9,caspase-3,cyt-c,cyclinD1,Bcl-2 et al other molecules related to proliferation and apoptosis in MDCC-MSB1 cells.Cell pro-liferation was detected by CCK-8 and cell cycle and apoptosis were detected by flow cytometry.The results showed that compared with the control group,the transcription levels of mdv1-miR-M4-5p,cyclinD1 and Bcl-2 in MDCC-MSB1 cells transfected with mdv1-miR-M4-5p mimics was significantly up-regulated.The transcription of TGF-β1,Smad2,cyt-c,caspase-9 and caspase-3 was down-regulated,the proliferation of MDCC-MSB1 cells was promoted,the the number of G1 phase cells were decreased,the S and G2 cells were increased,and the apoptosis rate was decreased.Compared with the control group,the results of the proliferation and apoptosis of MDCC-MSB1 cells and the expression of related molecules transfected with mdv1-miR-M4-5p inhibitor were opposite to those transfected with mdv1-miR-M4-5p mimics.The results showed that Mdv1-miR-M4-5p could promote the proliferation and inhibit the apoptosis of MDCC-MSB1 cells.This may be conducted by inhibiting the TGF-β1/Smad2 signaling pathway.

mdv1-miR-M4-5pMDVproliferationapoptosisTGF-β1/Smad2

余祖华、高梦茹、何雷、魏颖、陈建、陈松彪、丁轲

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河南科技大学动物科技学院/功能微生物与畜禽健康实验室/动物疫病与公共卫生重点实验室,洛阳 471023

洛阳市活载体生物材料与动物疫病防控重点实验室,洛阳 471023

河南科技学院动物科技学院,新乡 453003

mdv1-miR-M4-5p MDV 增殖 凋亡 TGF-β1/Smad2

国家自然科学基金国家自然科学基金

U150430831702207

2024

畜牧兽医学报
中国畜牧兽医学会

畜牧兽医学报

CSTPCD北大核心
影响因子:0.729
ISSN:0366-6964
年,卷(期):2024.55(8)