Sphingolipids as receptor modulators. An overview - PubMed (original) (raw)
Review
Sphingolipids as receptor modulators. An overview
A J Yates et al. Ann N Y Acad Sci. 1998.
Abstract
Glycosphingolipids are amphipathic compounds that exist mainly in the plasmalemma with their oligosaccharide portion protruding into the extracellular environment. In this position they are admirably situated for interacting with both ligands and receptors. Binding studies have demonstrated that specific glycolipids function as receptors for some microorganisms and bacterial toxins. Specific oligosaccharides on both glycolipids and glycoproteins bind members of the selection families, and some gangliosides facilitate integrins binding to their ligands. Gangliosides modulate the trophic factor-stimulated dimerization, tyrosine phosphorylation, and subsequent signal transduction events of several tyrosine kinase receptors. GM3 inhibits both the epidermal growth factor receptor and basic fibroblast factor receptor; several gangliosides except GM3 inhibit the platelet-derived growth-factor receptor; GM1 enhances nerve growth-factor-stimulated activation of TrkA; insulin receptor is inhibited to varying degrees by several gangliosides, but 2-->3 sialosylparagloboside is most effective. Activities of the beta(1)-adrenergic and delta-opioid receptors are modulated by GM1. Available information suggests that glycolipids serve as coordinators of multiple receptor functions.
Similar articles
- Ganglioside modulation of the PDGF receptor. A model for ganglioside functions.
Yates AJ, Saqr HE, Van Brocklyn J. Yates AJ, et al. J Neurooncol. 1995;24(1):65-73. doi: 10.1007/BF01052661. J Neurooncol. 1995. PMID: 8523078 Review. - Mechanisms through which gangliosides inhibit PDGF-stimulated mitogenesis in intact Swiss 3T3 cells: receptor tyrosine phosphorylation, intracellular calcium, and receptor binding.
Yates AJ, VanBrocklyn J, Saqr HE, Guan Z, Stokes BT, O'Dorisio MS. Yates AJ, et al. Exp Cell Res. 1993 Jan;204(1):38-45. doi: 10.1006/excr.1993.1006. Exp Cell Res. 1993. PMID: 8416794 - Gangliosides GM1, GM2 and GM3 inhibit the platelet-derived growth factor-induced signalling transduction pathway in vascular smooth muscle cells by different mechanisms.
Sachinidis A, Kraus R, Seul C, Meyer zu Brickwedde MK, Schulte K, Ko Y, Hoppe J, Vetter H. Sachinidis A, et al. Eur J Cell Biol. 1996 Sep;71(1):79-88. Eur J Cell Biol. 1996. PMID: 8884181 - Glycolipids of a human glioma cell line bearing receptors for platelet-derived growth factor (PDGF).
Yates AJ, Agudelo JD, Sung CC. Yates AJ, et al. Lipids. 1992 Apr;27(4):308-10. doi: 10.1007/BF02536482. Lipids. 1992. PMID: 1325593 - Lubricating cell signaling pathways with gangliosides.
Allende ML, Proia RL. Allende ML, et al. Curr Opin Struct Biol. 2002 Oct;12(5):587-92. doi: 10.1016/s0959-440x(02)00376-7. Curr Opin Struct Biol. 2002. PMID: 12464309 Review.
Cited by
- Cholesterol-Dependent Serotonin Insertion Controlled by Gangliosides in Model Lipid Membranes.
Fantini J, Azzaz F, Bennaï R, Yahi N, Chahinian H. Fantini J, et al. Int J Mol Sci. 2024 Sep 23;25(18):10194. doi: 10.3390/ijms251810194. Int J Mol Sci. 2024. PMID: 39337677 Free PMC article. - Leveraging altered lipid metabolism in treating B cell malignancies.
Lee J, Mani A, Shin MJ, Krauss RM. Lee J, et al. Prog Lipid Res. 2024 Jul;95:101288. doi: 10.1016/j.plipres.2024.101288. Epub 2024 Jul 2. Prog Lipid Res. 2024. PMID: 38964473 Free PMC article. Review. - The cancer glycocode as a family of diagnostic biomarkers, exemplified by tumor-associated gangliosides.
Nejatie A, Yee SS, Jeter A, Saragovi HU. Nejatie A, et al. Front Oncol. 2023 Oct 26;13:1261090. doi: 10.3389/fonc.2023.1261090. eCollection 2023. Front Oncol. 2023. PMID: 37954075 Free PMC article. Review. - Ganglioside GM1 and the Central Nervous System.
Guo Z. Guo Z. Int J Mol Sci. 2023 May 31;24(11):9558. doi: 10.3390/ijms24119558. Int J Mol Sci. 2023. PMID: 37298512 Free PMC article. Review. - Glycosphingolipids.
Chiricozzi E, Aureli M, Mauri L, Di Biase E, Lunghi G, Fazzari M, Valsecchi M, Carsana EV, Loberto N, Prinetti A, Sonnino S. Chiricozzi E, et al. Adv Exp Med Biol. 2021;1325:61-102. doi: 10.1007/978-3-030-70115-4_3. Adv Exp Med Biol. 2021. PMID: 34495530
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials