General structures of sphingolipids

Sphingolipids, or glycosylceramides, are a class of lipids containing a backbone of sphingoid bases, a set of aliphatic amino alcohols that includes sphingosine. They were discovered in brain extracts in the 1870s and were named for the mythological Sphinx because of their enigmatic nature.[1] These compounds play important roles in signal transmission and cell recognition. Sphingolipidoses, or disorders of sphingolipid metabolism, have particular impact on neural tissue. A sphingolipid with an R group consisting of a hydrogen atom only is a ceramide. Other common R groups include phosphocholine, yielding a sphingomyelin, and various sugar monomers or dimers, yielding cerebrosides and globosides, respectively. Cerebrosides and globosides are collectively known as glycosphingolipids.


  • Structure 1
  • Types 2
  • Mammalian sphingolipid metabolism 3
  • Functions of mammalian sphingolipids 4
  • Yeast sphingolipids 5
  • Plant sphingolipids 6
  • Disorders 7
  • Additional images 8
  • References 9
  • External links 10


The long-chain bases, sometimes simply known as sphingoid bases, are the first non-transient products of de novo sphingolipid synthesis in both yeast and mammals. These compounds, specifically known as phytosphingosine and dihydrosphingosine (also known as sphinganine,[2] although this term is less common), are mainly C18 compounds, with somewhat lower levels of C20 bases.[3] Ceramides and glycosphingolipids are N-acyl derivatives of these compounds.[4]

The sphingosine backbone is O-linked to a (usually) charged head group such as ethanolamine, serine, or choline.

The backbone is also amide-linked to an acyl group, such as a fatty acid.


Simple sphingolipids, which include the sphingoid bases and ceramides, make up the early products of the sphingolipid synthetic pathways.

  • Sphingoid bases are the fundamental building blocks of all sphingolipids. The main mammalian sphingoid bases are dihydrosphingosine and sphingosine, while dihydrosphingosine and phytosphingosine are the principle sphingoid bases in yeast.[5][6] Sphingosine, dihydrosphingosine, and phytosphingosine may be phosphorylated.
  • Ceramides, as a general class, are N-acylated sphingoid bases lacking additional head groups.
    • Dihydroceramide is produced by N-acylation of dihydrosphingosine. Dihydroceramide is found in both yeast and mammalian systems.
    • Ceramide is produced in mammalian systems by desaturation of dihydroceramide by dihydroceramide desaturase 1 (DES1). This highly bioactive molecule may also be phosphorylated to form ceramide-1-phosphate.
    • Phytoceramide is produced in yeast by hydroxylation of dihydroceramide at C-4.

Complex sphingolipids may be formed by addition of head groups to ceramide or phytoceramide:

Mammalian sphingolipid metabolism

De novo sphingolipid synthesis begins with formation of 3-keto-dihydrosphingosine by serine palmitoyltransferase.[7] The preferred substrates for this reaction are palmitoyl-CoA and serine. However, studies have demonstrated that serine palmitoyltransferase has some activity toward other species of fatty acyl-CoA[8] and alternative amino acids,[9] and the diversity of sphingoid bases has recently been reviewed.[10] Next, 3-keto-dihydrosphingosine is reduced to form dihydrosphingosine. Dihydrosphingosine is acylated by a (dihydro)-ceramide synthase, such as Lass1p or Lass2p (also termed as CerS), to form dihydroceramide.[11] This is desaturated to form ceramide.[12]

Metabolic pathways of various forms of sphingolipids. Sphingolipidoses are labeled at corresponding stages that are deficient.

Ceramide may subsequently have several fates. It may be phosphorylated by ceramide kinase to form ceramide-1-phosphate. Alternatively, it may be glycosylated by glucosylceramide synthase or galactosylceramide synthase. Additionally, it can be converted to sphingomyelin by the addition of a phosphorylcholine headgroup by sphingomyelin synthase. Diacylglycerol is generated by this process. Finally, ceramide may be broken down by a ceramidase to form sphingosine. Sphingosine may be phosphorylated to form sphingosine-1-phosphate. This may be dephosphorylated to reform sphingosine.[13]

Breakdown pathways allow the reversion of these metabolites to ceramide. The complex glycosphingolipids are hydrolyzed to glucosylceramide and galactosylceramide. These lipids are then hydrolyzed by beta-glucosidases and beta-galactosidases to regenerate ceramide. Similarly, sphingomyelin may be broken down by sphingomyelinase to form ceramide.

The only route by which sphingolipids are converted to non-sphingolipids is through sphingosine-1-phosphate lyase. This forms ethanolamine phosphate and hexadecenal.[14]

Functions of mammalian sphingolipids

Sphingolipids are commonly believed to protect the cell surface against harmful environmental factors by forming a mechanically stable and chemically resistant outer leaflet of the plasma membrane lipid bilayer. Certain complex glycosphingolipids were found to be involved in specific functions, such as cell recognition and signaling. Cell recognition depends mainly on the physical properties of the sphingolipids, whereas signaling involves specific interactions of the glycan structures of glycosphingolipids with similar lipids present on neighboring cells or with proteins.

Recently, simple sphingolipid

External links

  1. ^ Chun, J.; Hartung, H.P. (2010). "Mechanism of Action of Oral Fingolimod (FTY720) in Multiple Sclerosis". Clin. Neuropharmacol 33 (2): 91–101.  
  2. ^ Product page at Sigma Aldrich
  3. ^ Reviewed in Dickson, R.C. (1998) Annual Review of Biochemistry 67, 27-48.
  4. ^ A brief, very comprehensible review is given in Gunstone, F. (1996) Fatty Acid and Lipid Chemistry, pp 43-44. Blackie Academic and Professional. ISBN 0-7514-0253-2
  5. ^ Dickson, Robert C. "New insights into sphingolipid metabolism and function in budding yeast." J Lipid Res. (2008) 49, 909-921. doi:10.1194/jlr.R800003-JLR200
  6. ^ Bartke N and Y. Hannun. "Bioactive sphingolipids: metabolism and function." J Lipid Res. (2009) 50 Suppl:S91-6. doi:10.1194/jlr.R800080-JLR200
  7. ^ Merrill. "Characterization of serine palmitoyltransferase activity in Chinese hamster ovary cells." Biochim Biophys Acta (1983) 754(3):284-91.
  8. ^ Merrill and Williams. "Utilization of different fatty acyl-CoA thioesters by serine palmitoyltransferase from rat brain". Journal of Lipid Research (1984) 25 (2): 185-188.
  9. ^ Zitomer NC, Mitchell T, Voss KA, Bondy GS, Pruett ST, Garnier-Amblard EC, Liebeskind LS, Park H, Wang E, Sullards MC, Merrill AH Jr, Riley RT. "Ceramide Synthase Inhibition by Fumonisin B1 Causes Accumulation of 1-Deoxysphinganine: A Novel Category of Bioactive 1-Deoxysphingoid Bases And 1-Deoxydihydroceramides Biosynthesized By Mammalian Cell Lines And Animals". Journal of Biological Chemistry (2009) 284 (8): 4786-4795.
  10. ^ Pruett et al. "Biodiversity of sphingoid bases ("sphingosines") and related amino alcohols". Journal of Lipid Research. (2008) 49:1621-1639.
  11. ^ Pewzner-Jung et al. "When do Lasses (longevity assurrance genes) become CerS (ceramide synthases)?: insights into the regulation of ceramide synthesis". Journal of Biological Chemistry. (2006) 281, 25001-25005.
  12. ^ Causeret et al. "Further characterization of rat dihydroceramide desaturase: tissue distribution, subcellular localization, and substrate specificity". Lipids. (2005) 35:1117-1125.
  13. ^ Reviewed in Hannun and Obeid. "Principles of bioactive lipid signalling: lessons from sphingolipids". Nature Reviews Molecular Cell Biology. (2008) 9, 139-150.
  14. ^ Bandhuvulua & Saba. "Sphingosine-1-phosphate lyase in immunity and cancer: silencing the siren". Trends in Molecular Medicine. (2007) 13:210-217.
  15. ^ Hannun YA, Obeid LM (July 2002). "The Ceramide-centric universe of lipid-mediated cell regulation: stress encounters of the lipid kind". J. Biol. Chem. 277 (29): 25847–50.  
  16. ^ Spiegel S, Milstien S (July 2002). "Sphingosine 1-phosphate, a key cell signaling molecule". J. Biol. Chem. 277 (29): 25851–4.  
  17. ^ Lavieu G, Scarlatti F, Sala G, Carpentier S, Levade T, Ghidoni R, Botti J, Codogno P. "Regulation of autophagy by sphingosine kinase 1 and its role in cell survival during nutrient starvation." J Biol Chem. (2006) 281(13):8518-27. doi:10.1074/jbc.M506182200
  18. ^ Venable, M. E.; Lee, J. Y.; Smyth, M. J.; Bielawska, A.; Obeid, L. M. (1995). "Role of ceramide in cellular senescence". J. Biol. Chem. 270: 30701–30708.  
  19. ^ Hetz, C. A.; Hunn, M.; Rojas, P.; Torres, V.; Leyton, L.; Quest, A. F. (2002). "Caspase-dependent initiation of apoptosis and necrosis by the Fas receptor in lymphoid cells: onset of necrosis is associated with delayed ceramide increase". J. Cell Sci. 115: 4671–4683.  
  20. ^ Snider, AJ; Orr Gandy, KA; Obeid, LM (2010). "Sphingosine kinase: Role in regulation of bioactive sphingolipid mediators in inflammation". Biochimie 92 (6): 707–15.  
  21. ^ Brown DA, London E (June 2000). "Structure and function of sphingolipid- and cholesterol-rich membrane rafts". J. Biol. Chem. 275 (23): 17221–4.  
  22. ^ Futerman AH (December 2006). "Intracellular trafficking of sphingolipids: relationship to biosynthesis". Biochim. Biophys. Acta 1758 (12): 1885–92.  
  23. ^ van Meer G, Lisman Q (July 2002). "Sphingolipid transport: rafts and translocators". J. Biol. Chem. 277 (29): 25855–8.  
  24. ^ "Sphingolipids in Food and the Emerging Importance of Sphingolipids to Nutrition". July 15, 2013. 
  25. ^ Chung, N (2001). "Phytosphingosine as a specific inhibitor of growth and nutrient import in Saccharomyces cerevisiae". J Biol Chem 276 (38): 35614–21.  
  26. ^ Cowart; Obeid (2007). "Yeast sphingolipids: recent developments in understanding biosynthesis, regulation, and function". Biochim Biophys Acta. 1771 (3): 421–31.  
  27. ^ Dickson, RC (2008). J Lipid Res 49 (5): 909–21. 
  28. ^ Brice; Cowart (2009). J Biol Chem. 


Additional images

There are several disorders of sphingolipid metabolism, known as sphingolipidoses. The main members of this group are Niemann-Pick disease, Fabry disease, Krabbe disease, Gaucher disease, Tay-Sachs disease and Metachromatic leukodystrophy. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-linked. Taken together, sphingolipidoses have an incidence of approximately 1 in 10,000, but substantially more in certain populations such as Ashkenazi Jews. Enzyme replacement therapy is available to treat mainly Fabry disease and Gaucher disease, and people with these types of sphingolipidoses may live well into adulthood. The other types are generally fatal by age 1 to 5 years for infantile forms, but progression may be mild for juvenile- or adult-onset forms.


Higher plants contain a wider variety of sphingolipids than animals and fungi.

Plant sphingolipids

In addition to the important structural functions of complex sphingolipids (inositol phosphorylceramide and its mannosylated derivatives), the sphingoid bases phytosphingosine and dihydrosphingosine (sphinganine) play vital signaling roles in S. cerevisiae. These effects include regulation of endocytosis, ubiquitin-dependent proteolysis (and, thus, regulation of nutrient uptake [25]), cytoskeletal dynamics, the cell cycle, translation, posttranslational protein modification, and the heat stress response.[26] Additionally, modulation of sphingolipid metabolism by phosphatidylinositol (4,5)-bisphosphate signaling via Slm1p and Slm2p and calcineurin has recently been described.[27] Additionally, a substrate-level interaction has been shown between complex sphingolipid synthesis and cycling of phosphatidylinositol 4-phosphate by the phosphatidylinositol kinase Stt4p and the lipid phosphatase Sac1p.[28]

Because of the incredible complexity of mammalian systems, yeast are often used as a open reading frame single deletion. The two most commonly used yeasts are Saccharomyces cerevisiae and Schizosaccharomyces pombe, although research is also done in the pathological yeast Candida albicans.

Yeast sphingolipids

In experimental animals, feeding sphingolipids inhibits colon carcinogenesis, reduces (bad) LDL cholesterol and elevates (good) HDL cholesterol.[24]

Sphingolipids are synthesized in a pathway that begins in the ER and is completed in the Golgi apparatus, but these lipids are enriched in the plasma membrane and in endosomes, where they perform many of their functions.[22] Transport occurs via vesicles and monomeric transport in the cytosol. Sphingolipids are virtually absent from mitochondria and the ER, but constitute a 20-35 molar fraction of plasma membrane lipids.[23]