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病毒-宿主界面处的过氧化物酶体可塑性。

Peroxisome Plasticity at the Virus-Host Interface.

机构信息

Department of Molecular Biology, Princeton University, Lewis Thomas Laboratory, Washington Road, Princeton, NJ 08544, USA.

Department of Molecular Biology, Princeton University, Lewis Thomas Laboratory, Washington Road, Princeton, NJ 08544, USA.

出版信息

Trends Microbiol. 2019 Nov;27(11):906-914. doi: 10.1016/j.tim.2019.06.006. Epub 2019 Jul 19.

Abstract

Peroxisomes are multifunctional organelles with roles in cellular metabolism, cytotoxicity, and signaling. The plastic nature of these organelles allows them to respond to diverse biological processes, such as virus infections, by remodeling their biogenesis, morphology, and composition to enhance specific functions. During virus infections in humans, peroxisomes act as important immune signaling organelles, aiding the host by orchestrating antiviral signaling. However, more recently it was discovered that peroxisomes can also benefit the virus, facilitating virus-host interactions that rewire peroxisomes to support cellular processes for virus replication and spread. Here, we describe recent studies that uncovered this double-edged character of peroxisomes during infection, highlighting mechanisms that viruses have coevolved to take advantage of peroxisome plasticity. We also provide a perspective for future studies by comparing the established roles of peroxisomes in plant infections and discussing the promise of virology studies as a venue to reveal the uncharted biology of peroxisomes.

摘要

过氧化物酶体是多功能细胞器,在细胞代谢、细胞毒性和信号转导中发挥作用。这些细胞器的可塑性使它们能够通过重塑生物发生、形态和组成来应对多种生物过程,如病毒感染,从而增强特定功能。在人类的病毒感染过程中,过氧化物酶体作为重要的免疫信号细胞器,通过协调抗病毒信号来帮助宿主。然而,最近发现过氧化物酶体也可以使病毒受益,促进病毒-宿主相互作用,重塑过氧化物酶体以支持病毒复制和传播的细胞过程。在这里,我们描述了最近的研究,这些研究揭示了感染过程中过氧化物酶体的这种双刃剑特性,强调了病毒共同进化以利用过氧化物酶体可塑性的机制。我们还通过比较植物感染中过氧化物酶体的既定作用,并讨论病毒学研究作为揭示过氧化物酶体未知生物学的一个场所的潜力,为未来的研究提供了一个视角。

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