A new turning point in glycosphingolipid research
- PMID: 17022144
- DOI: 10.1111/j.1749-0774.2005.tb00002.x
A new turning point in glycosphingolipid research
Abstract
Research on glycosphingolipids has advanced with the finding of their involvement in sphingolipidoses, blood group- and differentiation-related antigens, and receptors for bacteria and viruses. Recently, the molecular cloning of genes for the synthesis of glycosphingolipids has been performed extensively, and mice without sugar transferase-genes have been generated. These transferase-null mice have shown that the complex carbohydrate structures of glycosphingolipids are not essential for the embryogenesis, morphogenesis or development of animals, but that the accumulation of an intermediate, such as GM3 or ceramide, causes significant failure of neural development in knockout mice as to the GM2, GD3 and GlcCer synthase genes. On the other hand, the nonreducing terminal carbohydrates in either glycosphingolipids or glycoproteins have been confirmed to be related to carbohydrate-mediated phenomena using the same gene-manipulation technique, indicating that glycosphingolipids are some of the carriers for functionally important carbohydrates. Glycosphingolipids are certainly small molecules with hydrophobic ceramides, which carry both donor and acceptor groups of the hydrogen-bonding region with the potential ability to interact with several proteins on the raft structure in biomembranes, and their dynamic movement in the membranes was revealed by the flip-flop regulation of their synthesis in the Golgi apparatus and the transformation-associated alteration in the reactivity of the carbohydrate moiety with several ligands. Thus, research on the functional significance of glycosphingolipids should be carried out again regarding their physicochemical properties.
Similar articles
-
Glycosphingolipid functions.Cold Spring Harb Perspect Biol. 2011 Jul 1;3(7):a004788. doi: 10.1101/cshperspect.a004788. Cold Spring Harb Perspect Biol. 2011. PMID: 21555406 Free PMC article. Review.
-
Role of Ceramide from Glycosphingolipids and Its Metabolites in Immunological and Inflammatory Responses in Humans.Mediators Inflamm. 2015;2015:120748. doi: 10.1155/2015/120748. Epub 2015 Nov 1. Mediators Inflamm. 2015. PMID: 26609196 Free PMC article. Review.
-
Recent advances in the biochemistry of sphingolipidoses.Brain Pathol. 1998 Jan;8(1):79-100. doi: 10.1111/j.1750-3639.1998.tb00138.x. Brain Pathol. 1998. PMID: 9458169 Free PMC article. Review.
-
Use of brefeldin A to define sites of glycosphingolipid synthesis: GA2/GM2/GD2 synthase is trans to the brefeldin A block.Proc Natl Acad Sci U S A. 1990 Sep;87(17):6838-42. doi: 10.1073/pnas.87.17.6838. Proc Natl Acad Sci U S A. 1990. PMID: 2118658 Free PMC article.
-
Structure, organization, and function of glycosphingolipids in membrane.Curr Opin Hematol. 2003 Jan;10(1):16-24. doi: 10.1097/00062752-200301000-00004. Curr Opin Hematol. 2003. PMID: 12483107 Review.
Cited by
-
Glycosphingolipids as receptors for non-enveloped viruses.Viruses. 2010 Apr;2(4):1011-1049. doi: 10.3390/v2041011. Epub 2010 Apr 15. Viruses. 2010. PMID: 21994669 Free PMC article.
-
Shotgun glycomics: a microarray strategy for functional glycomics.Nat Methods. 2011 Jan;8(1):85-90. doi: 10.1038/nmeth.1540. Epub 2010 Dec 5. Nat Methods. 2011. PMID: 21131969 Free PMC article.
-
Gangliosides in human, cow and goat milk, and their abilities as to neutralization of cholera toxin and botulinum type A neurotoxin.Glycoconj J. 2008 Oct;25(7):675-83. doi: 10.1007/s10719-008-9128-6. Epub 2008 May 23. Glycoconj J. 2008. PMID: 18498052
-
Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells.Bioorg Med Chem. 2010 Nov 1;18(21):7565-79. doi: 10.1016/j.bmc.2010.08.050. Epub 2010 Sep 28. Bioorg Med Chem. 2010. PMID: 20851613 Free PMC article.
-
Spermatogenesis-associated changes of fucosylated glycolipids in murine testis.Hum Cell. 2020 Jan;33(1):23-28. doi: 10.1007/s13577-019-00304-x. Epub 2019 Nov 29. Hum Cell. 2020. PMID: 31784953
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources