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支原体核酸酶 MGA_0676 诱导鸡胚成纤维细胞凋亡的机制。

Mechanism of Apoptosis Induction by Mycoplasmal Nuclease MGA_0676 in Chicken Embryo Fibroblasts.

机构信息

Key Laboratory of Animal Epidemiology and Zoonosis, College of Veterinary Medicine, China Agricultural University, Beijing, China.

Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agricultural and Forestry Sciences, Beijing, China.

出版信息

Front Cell Infect Microbiol. 2018 Apr 4;8:105. doi: 10.3389/fcimb.2018.00105. eCollection 2018.

Abstract

MGA_0676 has been characterized as a nuclease that can induce apoptosis of chicken cells. However, the mechanism by which MGA_0676 induces apoptosis has remained unclear. In this study, we evaluated MGA_0676-induced apoptosis and internalization in immortalized chicken embryo fibroblasts (DF-1) and cancer cell lines. The internalization of MGA_0676 was proven through caveolin-mediated endocytosis by blocking the endocytosis with specific inhibitors or with siRNA. We identified the Thif domain of NEDD8-activating enzyme E1 regulatory subunit (NAE) in DF-1 as the target region interacting with the SNC domain of MGA_0676. The interaction between the Thif and SNC domains was observed co-located in the perinuclear and nuclear of DF-1. We found that the interaction between NAE and MGA_0676 increased the ability of apoptosis and accelerated the process of cullin neddylation in DF-1 cells, in turn activating NF-κB. This resulted in the observed aggregation of NF-κB in the nuclei of DF-1 cells. Moreover, the apoptosis induced by MGA_0676 decreased significantly when NF-κB was inhibited by siRNA or BAY 11-7082 or when NAE was silenced by siRNA. Overall, our results demonstrate that MGA_0676 is internalized through caveolin-mediated endocytosis, interacts with SNC-dependent Thif to accelerate the process of cullin neddylation and activates NF-κB in DF-1 cells, ultimately playing a key role in apoptosis in chicken cells. Our results indicate MGA_0676 constitutes a critical etiological virulence factor of the respiratory disease caused by . This study also opens a venue to investigate MGA_0676 as a potential candidate as pro-apoptotic drug in cancer studies.

摘要

MGA_0676 被鉴定为一种能够诱导鸡细胞凋亡的核酸酶。然而,MGA_0676 诱导凋亡的机制仍不清楚。在本研究中,我们评估了 MGA_0676 在鸡胚成纤维细胞(DF-1)和癌细胞系中的诱导凋亡和内化作用。通过用特异性抑制剂或 siRNA 阻断内吞作用,证明了 MGA_0676 的内化是通过网格蛋白介导的内吞作用实现的。我们鉴定出 NEDD8 激活酶 E1 调节亚基(NAE)的 Thif 结构域是与 MGA_0676 的 SNC 结构域相互作用的靶区。在 DF-1 中观察到 Thif 和 SNC 结构域的相互作用位于核周和核内。我们发现,NAE 与 MGA_0676 之间的相互作用增加了凋亡的能力,并加速了 DF-1 细胞中 cullin neddylation 的过程,从而激活了 NF-κB。这导致观察到 NF-κB 在 DF-1 细胞核内聚集。此外,当用 siRNA 或 BAY 11-7082 抑制 NF-κB 或用 siRNA 沉默 NAE 时,MGA_0676 诱导的凋亡显著减少。总的来说,我们的研究结果表明,MGA_0676 通过网格蛋白介导的内吞作用被内化,与 SNC 依赖性 Thif 相互作用,加速 cullin neddylation 的过程,并激活 DF-1 细胞中的 NF-κB,最终在鸡细胞的凋亡中发挥关键作用。我们的研究结果表明,MGA_0676 是由引起的呼吸道疾病的关键病原毒力因子。本研究还为将 MGA_0676 作为癌症研究中潜在的促凋亡药物提供了一个研究途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b67/5893762/342a4f7bcc6d/fcimb-08-00105-g0001.jpg

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