Department of Microbiology and Immunology, German University inCairo, New Cairo, Egypt.
Department of Biochemistry, German University in Cairo, New Cairo, Egypt.
Int J Biochem Cell Biol. 2020 May;122:105738. doi: 10.1016/j.biocel.2020.105738. Epub 2020 Mar 7.
Viroporins are virus encoded proteins that alter membrane permeability and can trigger subsequent cellular signals. Oligomerization of viroporin subunits results in formation of a hydrophilic pore which facilitates ion transport across host cell membranes. These viral channel proteins may be involved in different stages of the virus infection cycle. Inflammasomes are large multimolecular complexes best recognized for their ability to control activation of caspase-1, which in turn regulates the maturation of interleukin-1 β (IL-1β) and interleukin 18 (IL-18). IL-1β was originally identified as a pro-inflammatory cytokine able to induce both local and systemic inflammation and a febrile reaction in response to infection or injury. Excessive production of IL-1β is associated with autoimmune and inflammatory diseases. Microbial derivatives, bacterial pore-forming toxins, extracellular ATP and other pathogen-associated molecular patterns trigger activation of NLRP3 inflammasomes. Recent studies have reported that viroporin activity is capable of inducing inflammasome activity and production of IL-1β, where NLRP3 is shown to be regulated by fluxes of K, H and Ca in addition to reactive oxygen species, autophagy and endoplasmic reticulum stress. The aim of this review is to present an overview of the key findings on viroporin activity with special emphasis on their role in virus immunity and as possible activators of inflammasomes.
病毒通道蛋白是病毒编码的蛋白,可改变膜通透性,并能引发后续的细胞信号。病毒通道蛋白亚基的寡聚化导致形成亲水性孔,从而促进离子穿过宿主细胞膜的转运。这些病毒通道蛋白可能参与病毒感染周期的不同阶段。炎症小体是大型多分子复合物,其最显著的特征是能够控制半胱天冬酶-1 的激活,而后者又调节白细胞介素-1β(IL-1β)和白细胞介素 18(IL-18)的成熟。IL-1β最初被鉴定为一种促炎细胞因子,能够诱导局部和全身炎症以及对感染或损伤的发热反应。IL-1β 的过度产生与自身免疫和炎症性疾病有关。微生物衍生物、细菌形成孔的毒素、细胞外 ATP 和其他病原体相关的分子模式触发 NLRP3 炎症小体的激活。最近的研究报告称,病毒通道蛋白的活性能够诱导炎症小体的活性和 IL-1β 的产生,其中 NLRP3 被证明除了活性氧、自噬和内质网应激之外,还受到 K、H 和 Ca 流的调节。本综述的目的是概述病毒通道蛋白活性的关键发现,特别强调其在病毒免疫中的作用以及作为炎症小体可能的激活剂的作用。