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酸性鞘磷脂酶的作用及鞘脂代谢调节在细菌感染中的作用。

The role of acid sphingomyelinase and modulation of sphingolipid metabolism in bacterial infection.

机构信息

Division of Hematology, University Hospital Zurich, Rämistrasse 100, 8091 Zürich, Switzerland.

Institute of Hygiene and Microbiology, University of Würzburg, Josef-Schneider-Straße 2, D-97080 Würzburg, Germany.

出版信息

Biol Chem. 2018 Sep 25;399(10):1135-1146. doi: 10.1515/hsz-2018-0200.

Abstract

Acid sphingomyelinase (ASM) is a key enzyme in sphingolipid metabolism that converts sphingomyelin to ceramide, thereby modulating membrane structures and signal transduction. Bacterial pathogens can manipulate ASM activity and function, and use host sphingolipids during multiple steps of their infection process. An increase in ceramides upon infection results in the formation of ceramide-enriched membrane platforms that serve to cluster receptor molecules and organize intracellular signaling molecules, thus facilitating bacterial uptake. In this review, we focus on how extracellular bacterial pathogens target ASM and modulate membrane properties and signaling pathways to gain entry into eukaryotic cells or induce cell death. We describe how intracellular pathogens interfere with the intralysosomal functions of ASM to favor replication and survival. In addition, bacteria utilize their own sphingomyelinases as virulence factors to modulate sphingolipid metabolism. The potential of ASM as a target for treating bacterial infections is also discussed.

摘要

酸性鞘磷脂酶(ASM)是鞘脂代谢中的关键酶,可将鞘磷脂转化为神经酰胺,从而调节膜结构和信号转导。细菌病原体可以操纵 ASM 的活性和功能,并在其感染过程的多个步骤中利用宿主鞘脂。感染后神经酰胺的增加导致富含神经酰胺的膜平台的形成,这些平台有助于聚集受体分子和组织细胞内信号分子,从而促进细菌摄取。在这篇综述中,我们重点介绍了细胞外细菌病原体如何靶向 ASM 并调节膜特性和信号通路,以进入真核细胞或诱导细胞死亡。我们描述了细胞内病原体如何干扰 ASM 的溶酶体功能,以促进复制和存活。此外,细菌还利用自身的鞘磷脂酶作为毒力因子来调节鞘脂代谢。还讨论了 ASM 作为治疗细菌感染的靶标的潜力。

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