FUMONISINS - FUNGAL TOXINS THAT SHED LIGHT ON SPHINGOLIPID FUNCTION

Citation
Ah. Merrill et al., FUMONISINS - FUNGAL TOXINS THAT SHED LIGHT ON SPHINGOLIPID FUNCTION, Trends in cell biology, 6(6), 1996, pp. 218-223
Citations number
52
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
09628924
Volume
6
Issue
6
Year of publication
1996
Pages
218 - 223
Database
ISI
SICI code
0962-8924(1996)6:6<218:F-FTTS>2.0.ZU;2-P
Abstract
Fumonisins are sphinganine analogues produced by Fusarium moniliforme and related fungi. They inhibit ceramide synthase and block the biosyn thesis of complex sphingolipids, promoting accumulation of sphinganine and sphinganine I-phosphate. Disruption of sphingolipid metabolism by fumonisin B-1 alters cell-cell interactions, the behaviour of cell-su rface proteins, the activity of protein kinases, the metabolism of oth er lipids, and cell growth and viability. This multitude of effects pr obably accounts for the toxicity and carcinogenicity of these mycotoxi ns. Naturally occurring inhibitors of sphingolipid metabolism such as fumonisins are proving to be powerful tools for studying the diverse r oles of sphingolipids in cell regulation and disease.