McKenna Savannah, Jung Kwang Il, Wolf Jennifer J, Seo Young-Jin, Hahm Bumsuk
Departments of Surgery & Molecular Microbiology and Immunology, University of Missouri, Columbia, MO, 65212, USA.
Department of Life Science, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul, 06974, Republic of Korea.
Virology. 2025 Feb;603:110367. doi: 10.1016/j.virol.2024.110367. Epub 2024 Dec 22.
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.
鞘脂网络主要由生物活性鞘脂分子的平衡及其受鞘脂代谢酶的调节维持。脂质系统中的成分在包括病毒感染在内的众多细胞和疾病状况中发挥关键作用。在新冠疫情期间,人们做出了卓有成效的努力,使用一种阻断鞘氨醇激酶(SphK)2活性的抑制剂来治疗这种毁灭性疾病。对该抑制剂的支持来自于对流感的临床前研究,在该研究中,该抑制剂证明能有效保护小鼠免受流感引起的发病和死亡。这凸显了鞘脂系统的基础研究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传播。在这篇综述中,重点关注这些影响流感病毒生命周期的酶的作用以及流感病毒与鞘脂途径之间相互作用的可能机制。