Chemistry:Alpha-galactosylceramide

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Alpha-galactosylceramide
Alphagalactosylceramide
Names
IUPAC name
N-[(2S,3S,4R)-3,4-Dihydroxy-1-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadecan-2-yl]hexacosanamide
Other names
a-GalCer, KRN7000
Identifiers
3D model (JSmol)
7326597
ChEBI
ChEMBL
UNII
Properties
C50H99NO9
Molar mass 858.34
Appearance white powder
Melting point 189-190°C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

alpha-galactosylceramide (a-GalCer, KRN7000) is a synthetic glycolipid derived from structure-activity relationship studies of galactosylceramides isolated from the marine sponge Agelas mauritianus. a-GalCer is a strong immunostimulant and shows potent anti-tumour activity in many in vivo models[1].

Immunostimulatory properties

a-GalCer is a potent activator of iNKT cells, and a model CD1d antigen. The invariant T cell receptor of the iNKT cell is able to bind the CD1d:glycolipid complex leading to iNKT cell in both mice and humans[2].

Adjuvant activity

In combination with a peptide antigen, a-GalCer is able to stimulate a strong immune response against this epitope. The CD1d:glycolipid:TCR interaction activates the iNKT cell which can then activate the dendritic cell. This causes the release of a range of cytokines and licenses the dendritic cell to activate a peptide-specific T cell response. This adjuvant acts through this cellular interaction, rather than through classic pattern recognition receptor pathways[3].

References

  1. Morita, Masahiro; Motoki, Kazuhiro; Akimoto, Kohji; Natori, Takenori; Sakai, Teruyuki; Sawa, Eiji; Yamaji, Kazuo; Koezuka, Yasuhiko et al. (1995-06-01). "Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice". Journal of Medicinal Chemistry 38 (12): 2176–2187. doi:10.1021/jm00012a018. ISSN 0022-2623. https://doi.org/10.1021/jm00012a018. 
  2. Godfrey, Dale I.; Kronenberg, Mitchell (2004-11-15). "Going both ways: Immune regulation via CD1d-dependent NKT cells" (in en). Journal of Clinical Investigation 114 (10): 1379–1388. doi:10.1172/jci23594. ISSN 0021-9738. PMC 525753. https://doi.org/10.1172/JCI200423594. 
  3. Cerundolo, Vincenzo; Silk, Jonathan D.; Masri, S. Hajar; Salio, Mariolina (January 2009). "Harnessing invariant NKT cells in vaccination strategies" (in En). Nature Reviews Immunology 9 (1): 28–38. doi:10.1038/nri2451. ISSN 1474-1741. http://www.nature.com/articles/nri2451.