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猪流行性腹泻病毒通过 p53 依赖性途径导致细胞周期停滞在 G0/G1 期。

Porcine epidemic diarrhea virus through p53-dependent pathway causes cell cycle arrest in the G0/G1 phase.

机构信息

College of Animal Science and Technology, Anhui Agricultural University, Hefei, Anhui, 230036, China.

College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, 712100, China.

出版信息

Virus Res. 2018 Jul 15;253:1-11. doi: 10.1016/j.virusres.2018.05.019. Epub 2018 May 22.

Abstract

Porcine epidemic diarrhea virus (PEDV), an enteropathogenic Alphacoronavirus, has caused enormous economic losses in the swine industry. p53 protein exists in a wide variety of animal cells, which is involved in cell cycle regulation, apoptosis, cell differentiation and other biological functions. In this study, we investigated the effects of PEDV infection on the cell cycle of Vero cells and p53 activation. The results demonstrated that PEDV infection induces cell cycle arrest at G0/G1 phase in Vero cells, while UV-inactivated PEDV does not cause cell cycle arrest. PEDV infection up-regulates the levels of p21, cdc2, cdk2, cdk4, Cyclin A protein and down-regulates Cyclin E protein. Further research results showed that inhibition of p53 signaling pathway can reverse the cell cycle arrest in G0/G1 phase induced by PEDV infection and cancel out the up-regulation of p21 and corresponding Cyclin/cdk mentioned above. In addition, PEDV infection of the cells synchronized in various stages of cell cycle showed that viral subgenomic RNA and virus titer were higher in the cells released from G0/G1 phase synchronized cells than that in the cells released from the G1/S phase and G2/M phase synchronized or asynchronous cells after 18 h p.i.. This is the first report to demonstrate that the p53-dependent pathway plays an important role in PEDV induced cell cycle arrest and beneficially contributes to viral infection.

摘要

猪流行性腹泻病毒(PEDV)是一种能引起猪肠道疾病的α冠状病毒,它给养猪业造成了巨大的经济损失。p53 蛋白存在于多种动物细胞中,参与细胞周期调控、细胞凋亡、细胞分化等多种生物学功能。本研究探讨了 PEDV 感染对 Vero 细胞周期和 p53 激活的影响。结果表明,PEDV 感染诱导 Vero 细胞周期停滞在 G0/G1 期,而 UV 灭活的 PEDV 则不会引起细胞周期停滞。PEDV 感染上调了 p21、cdc2、cdk2、cdk4、Cyclin A 蛋白的水平,下调了 Cyclin E 蛋白的水平。进一步的研究结果表明,抑制 p53 信号通路可以逆转 PEDV 感染引起的 G0/G1 期细胞周期阻滞,并消除上述 p21 及相应的 Cyclin/cdk 的上调。此外,将细胞周期同步于不同阶段后再感染 PEDV,发现与 G1/S 期和 G2/M 期同步或非同步细胞相比,从 G0/G1 期同步细胞释放的细胞中病毒亚基因组 RNA 和病毒滴度更高。这是首次报道 p53 依赖性途径在 PEDV 诱导的细胞周期阻滞中发挥重要作用,并有利于病毒感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84e0/7114671/cb66ad2944be/gr1_lrg.jpg

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