Abstract

Sphingolipids represent a class of structural related lipids involved in membrane biology and various cellular processes including cell growth, apoptosis, inflammation and migration. Over the past decade, sphingolipids have become the focus of intensive studies regarding their involvement in infectious diseases. Pathogens can manipulate the sphingolipid metabolism resulting in cell membrane reorganization and receptor recruitment to facilitate their entry. They may recruit specific host sphingolipid metabolites to establish a favorable niche for intracellular survival and proliferation. In contrast, some sphingolipid metabolites can also act as a first line defense against bacteria based on their antimicrobial activity. In this review, we will focus on the strategies employed by pathogenic Neisseria spp. to modulate the sphingolipid metabolism and hijack the sphingolipid balance in the host to promote cellular colonization, invasion and intracellular survival. Novel techniques and innovative approaches will be highlighted that allow imaging of sphingolipid derivatives in the host cell as well as in the pathogen.

Highlights

  • Sphingolipids form a diverse group of structural related lipids, composed of a sphingoid backbone (sphingosine, dihydrosphingosine or phytosphingosine) coupled via an amid bond to a fatty acid side chain of various length

  • We recently revealed for the first time that the GSL monosialotetrahexosylganglioside (GM1) among the several gangliosides may serve as a receptor for N. meningitidis to invade the endothelium of the BCSFB [120]

  • Sphingolipids display a tremendous structural variety, which is reflected by their diverse involvement in cellular processes

Read more

Summary

Introduction

Sphingolipids form a diverse group of structural related lipids, composed of a sphingoid backbone (sphingosine, dihydrosphingosine (dhSph) or phytosphingosine) coupled via an amid bond to a fatty acid side chain of various length. The N-linked addition of a fatty acid to dhSph, catalyzed by dihydroceramide synthase, results in generation of dihydroceramide, which is subsequently desaturated to ceramide in mammalian cells. Thereverse reversereaction reactionis is catalyzed ceramide-1-phosphate phosphaceramide kinases. Ceramide can be converted to sphingosine, which can be phosphorylated by by sphingosine kinases to sphingosine-1-phosphate (S1P). The reverse reaction is catasphingosine kinases to sphingosine-1-phosphate is catalyzed lyzed by. (dihydro)sphingomyelin; CerK: ceramide kinase; C1P:ceramide ceramide 1-phosphate; ceramide 1-phosphate; CPP: ceramide 1-phosphate phosphatase; SphK: sphingosine kinase; S1P: sphingosine 1-phosCPP: ceramide 1-phosphate phosphatase; SphK: sphingosine kinase; S1P: sphingosine 1-phosphate; SPP: S1P phosphatase; phate; SPP: S1P phosphatase; aSMase: acid sphingmyelinase; nSMase: neutral sphingomyelinase 2.

Sphingomyelinases
Acid Sphingomyelinase
Neutral Sphingomyelinase
Sphingosine Kinases
11. Conclusions and Outlook
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call