Multiple sphingolipid-metabolizing enzymes modulate influenza virus replication.

Savannah McKenna, Kwang Il Jung, Jennifer J Wolf, Young-Jin Seo, Bumsuk Hahm
{"title":"Multiple sphingolipid-metabolizing enzymes modulate influenza virus replication.","authors":"Savannah McKenna, Kwang Il Jung, Jennifer J Wolf, Young-Jin Seo, Bumsuk Hahm","doi":"10.1016/j.virol.2024.110367","DOIUrl":null,"url":null,"abstract":"<p><p>The sphingolipid network is sustained principally by the balance of bioactive sphingolipid molecules and their regulation by sphingolipid-metabolizing enzymes. The components in the lipid system display key functions in numerous cellular and disease conditions including virus infections. During the COVID-19 pandemic, there was a fruitful effort to use an inhibitor that blocks the activity of sphingosine kinase (SphK) 2 to cure the devastating disease. Support for the inhibitor came from pre-clinical research on influenza where the inhibitor demonstrated effective protection of mice from influenza-induced morbidity and mortality. This highlights the importance of basic and translational research on the sphingolipid system for improving human health. Multiple sphingolipid-metabolizing enzymes have been reported to regulate influenza virus replication and propagation. In this review, the emphasis is placed on the roles of these enzymes that impact influenza virus life cycle and the conceivable mechanisms for the interplay between influenza virus and the sphingolipid pathway.</p>","PeriodicalId":94266,"journal":{"name":"Virology","volume":"603 ","pages":"110367"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.virol.2024.110367","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The sphingolipid network is sustained principally by the balance of bioactive sphingolipid molecules and their regulation by sphingolipid-metabolizing enzymes. The components in the lipid system display key functions in numerous cellular and disease conditions including virus infections. During the COVID-19 pandemic, there was a fruitful effort to use an inhibitor that blocks the activity of sphingosine kinase (SphK) 2 to cure the devastating disease. Support for the inhibitor came from pre-clinical research on influenza where the inhibitor demonstrated effective protection of mice from influenza-induced morbidity and mortality. This highlights the importance of basic and translational research on the sphingolipid system for improving human health. Multiple sphingolipid-metabolizing enzymes have been reported to regulate influenza virus replication and propagation. In this review, the emphasis is placed on the roles of these enzymes that impact influenza virus life cycle and the conceivable mechanisms for the interplay between influenza virus and the sphingolipid pathway.

多种鞘脂代谢酶调节流感病毒的复制。
鞘脂网络的维持主要依靠生物活性鞘脂分子的平衡和鞘脂代谢酶对其的调节。脂质系统中的成分在包括病毒感染在内的许多细胞和疾病条件中显示出关键功能。在2019冠状病毒病大流行期间,使用阻断鞘氨醇激酶(SphK) 2活性的抑制剂来治疗这种毁灭性疾病的努力取得了丰硕成果。对该抑制剂的支持来自流感的临床前研究,该抑制剂证明了对流感引起的小鼠发病率和死亡率的有效保护。这突出了鞘脂系统的基础和转化研究对改善人类健康的重要性。据报道,多种鞘脂代谢酶可调节流感病毒的复制和繁殖。本文就这些酶在影响流感病毒生命周期中的作用以及流感病毒与鞘脂通路相互作用的可能机制进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信