» Articles » PMID: 15207830

Glycosphingolipids As Toxin Receptors

Overview
Date 2004 Jun 23
PMID 15207830
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

A number of proteins produced by certain bacteria and plants are potently toxic to mammalian cells. This toxicity results from their ability to catalytically modify macromolecules that are required for essential cellular functions such as vesicular trafficking, cytoskeletal assembly, signalling or protein synthesis. To reach their targets, these proteins bind specific surface receptors before endocytosis and translocation across an internal membrane. The surface receptors exploited by different toxins include a range of proteins and lipids. Here we focus on specific glycosphingolipid receptors and two well-characterised subsets of toxins that exploit them for surface binding, intracellular trafficking, and signalling events.

Citing Articles

Mysterious sphingolipids: metabolic interrelationships at the center of pathophysiology.

Jamjoum R, Majumder S, Issleny B, Stiban J Front Physiol. 2024; 14:1229108.

PMID: 38235387 PMC: 10791800. DOI: 10.3389/fphys.2023.1229108.


Bacterial toxins and heart function: heat-labile enterotoxin B promotes changes in cardiac function with possible relevance for sudden cardiac death.

Ferreira G, Cardozo R, Sastre S, Costa C, Santander A, Chavarria L Biophys Rev. 2023; 15(4):447-473.

PMID: 37681088 PMC: 10480140. DOI: 10.1007/s12551-023-01100-6.


Glycomimetics for the inhibition and modulation of lectins.

Leusmann S, Menova P, Shanin E, Titz A, Rademacher C Chem Soc Rev. 2023; 52(11):3663-3740.

PMID: 37232696 PMC: 10243309. DOI: 10.1039/d2cs00954d.


A bispecific, crosslinking lectibody activates cytotoxic T cells and induces cancer cell death.

Rosato F, Pasupuleti R, Tomisch J, Melendez A, Kolanovic D, Makshakova O J Transl Med. 2022; 20(1):578.

PMID: 36494671 PMC: 9733292. DOI: 10.1186/s12967-022-03794-w.


Microbial lectome versus host glycolipidome: How pathogens exploit glycosphingolipids to invade, dupe or kill.

Bereznicka A, Mikolajczyk K, Czerwinski M, Kaczmarek R Front Microbiol. 2022; 13:958653.

PMID: 36060781 PMC: 9437549. DOI: 10.3389/fmicb.2022.958653.