鞘氨醇激酶
生物
1-磷酸鞘氨醇
病毒复制
鞘氨醇
鞘氨醇激酶1
细胞生物学
鞘脂
激酶
S1PR1型
病毒进入
鞘氨醇-1-磷酸受体
信号转导
病毒
受体
病毒学
遗传学
癌症研究
血管内皮生长因子A
血管内皮生长因子
血管内皮生长因子受体
作者
Lu Zhang,Juan Liu,Erya Xiao,Qingzhen Han,Lin Wang
摘要
Abstract Viruses can create a unique cellular environment that facilitates replication and transmission. Sphingosine kinases (SphKs) produce sphingosine‐1‐phosphate (S1P), a bioactive sphingolipid molecule that performs both physiological and pathological effects primarily by activating a subgroup of the endothelial differentiation gene family of G‐protein coupled cell surface receptors known as S1P receptors (S1PR1‐5). A growing body of evidence indicates that the SphK/S1P axis is crucial for regulating cellular activities in virus infections like respiratory viruses, enteroviruses, hepatitis viruses, herpes viruses, and arboviruses replicate. Depending on the type of virus, pro‐ or anti‐viral activities of the SphK/S1P axis sometimes rely on the host immune system and sometimes directly through intracellular signalling pathways or cell proliferation. Recent research has shown novel roles of S1P and SphK in viral replication. Sphingosine kinase isoforms (SphK1 and SphK2) levels can be manipulated by several viruses to promote the effects that are expected. Regulation of cellular signalling pathways plays a significant role in the mechanism. The purpose of this review is to provide insight of the characters played by the SphK/S1P axis throughout diverse viral infection processes. We then assess potential therapeutic methods that are based on S1P signalling and metabolism during viral infections.
科研通智能强力驱动
Strongly Powered by AbleSci AI