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双色茧蜂质型多角体病毒通过调节细胞 cyclophilin A-凋亡诱导因子相互作用诱导昆虫免疫抑制过程中的细胞凋亡。

Microplitis bicoloratus bracovirus regulates cyclophilin A-apoptosis-inducing factor interaction to induce cell apoptosis in the insect immunosuppressive process.

机构信息

School of Life Sciences, Yunnan University, Kunming, China.

Key Laboratory of the University in Yunnan Province for International Cooperation in Intercellular Communications and Regulations, Yunnan University, Kunming, China.

出版信息

Arch Insect Biochem Physiol. 2022 May;110(1):e21877. doi: 10.1002/arch.21877. Epub 2022 Feb 25.

Abstract

Microplitis bicoloratus bracovirus (MbBV) induces apoptosis in hemocytes of the host (Spodoptera litura) via the cyclophilin A (CypA)-mediated signaling pathway. However, the mechanisms underlying CypA-mediated signaling during apoptosis remain largely unknown. Therefore, in this study, we investigated how CypA and apoptosis-inducing factor (AIF) interact during MbBV-mediated apoptosis. Our findings showed that MbBV induces apoptosis through the CypA-AIF axis of insect immune suppression. In MbBV-infected Spli221 cells, both the expression of the cypa gene and the release of AIF from the mitochondria increased the number of apoptotic cells. CypA and AIF underwent concurrent cytoplasm-nuclear translocation. Conversely, blocking of AIF release from mitochondria not only inhibited the CypA-AIF interaction but also inhibited the cytoplasmic-nuclear translocation of AIF and CypA. Importantly, the survival of the apoptotic phenotype was significantly rescued in MbBV-infected Spli221 cells. In addition, we found that the cyclosporine A-mediated inhibition of CypA did not prevent the formation of the CypA and AIF complex; rather, this only suppressed genomic DNA fragmentation. In vitro experiments revealed direct molecular interactions between recombinant CypA and AIF. Taken together, our results demonstrate that the CypA-AIF interaction plays an important role in MbBV-induced innate immune suppression. This study will help to clarify aspects of insect immunological mechanisms and will be relevant to biological pest control.

摘要

双色茧蜂病毒(MbBV)通过亲环素 A(CypA)介导的信号通路诱导宿主(斜纹夜蛾)血细胞凋亡。然而,CypA 介导的信号通路在凋亡过程中的机制在很大程度上尚不清楚。因此,在本研究中,我们研究了 CypA 和凋亡诱导因子(AIF)在 MbBV 介导的凋亡过程中如何相互作用。研究结果表明,MbBV 通过昆虫免疫抑制的 CypA-AIF 轴诱导凋亡。在 MbBV 感染的 Spli221 细胞中,cypa 基因的表达和 AIF 从线粒体的释放均增加了凋亡细胞的数量。CypA 和 AIF 同时发生细胞质-核易位。相反,阻止 AIF 从线粒体释放不仅抑制了 CypA-AIF 相互作用,而且抑制了 AIF 和 CypA 的细胞质-核易位。重要的是,MbBV 感染的 Spli221 细胞中凋亡表型的存活率得到显著挽救。此外,我们发现环孢菌素 A 介导的 CypA 抑制并没有阻止 CypA 和 AIF 复合物的形成;相反,这只是抑制了基因组 DNA 片段化。体外实验揭示了重组 CypA 和 AIF 之间的直接分子相互作用。总之,我们的研究结果表明,CypA-AIF 相互作用在 MbBV 诱导的先天免疫抑制中发挥重要作用。本研究将有助于阐明昆虫免疫机制的各个方面,并与生物防治相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9947/9285338/f38f36b8573b/ARCH-110-0-g003.jpg

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