Host defenses against metabolic endotoxaemia and their impact on lipopolysaccharide detection
| Autor: | Catherine McLaughlin, Clett Erridge, Tola A. Faraj |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
Lipopolysaccharides
0301 basic medicine Lipopolysaccharide 030106 microbiology Immunology Disease Type ii diabetes Structure-Activity Relationship 03 medical and health sciences chemistry.chemical_compound Human gut Neutralization Tests Diabetes mellitus medicine Animals Humans Immunology and Allergy Disease Resistance Alternative methods biology Fatty liver medicine.disease biology.organism_classification Endotoxemia Disease Models Animal Kinetics 030104 developmental biology chemistry Limulus Host-Pathogen Interactions Energy Metabolism Biomarkers |
| Zdroj: | International Reviews of Immunology. 36:125-144 |
| ISSN: | 1563-5244 0883-0185 |
| DOI: | 10.1080/08830185.2017.1280483 |
| Popis: | Bacterial endotoxin (lipopolysaccharide, LPS), is one of the most potent inducers of inflammatory signaling, yet it is abundant in the human gut and the modern diet. Small quantities of LPS routinely translocate from the gut lumen to the circulation (so-called metabolic endotoxaemia), and elevated plasma LPS concentrations are reported in a variety of chronic non-communicable diseases, including obesity, non-alcoholic fatty liver disease, atherosclerosis and type II diabetes. Murine models of experimentally-induced endotoxaemia and Toll-like receptor-4 deficiency suggest that endotoxin may promote the metabolic disturbances that underpin these diseases. However, as bioactive LPS is cleared rapidly from the circulation, and reported levels of endotoxin in human plasma vary widely, the potential relevance of metabolic endotoxaemia to human disease remains unclear. We here review insight into these questions gained from human and murine models of experimental endotoxaemia, focusing on the kinetics of LPS neutralization and its clearance from blood, the limitations of the widely used limulus assay and alternative methods for LPS quantitation. We conclude that although new methods for LPS measurement will be required to definitively quantify the extent of metabolic endotoxaemia in man, evidence from numerous approaches suggests that this molecule may play a key role in the development of diverse metabolic diseases. |
| Databáze: | OpenAIRE |
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