Skip to main content
Log in

Blood group glycosphingolipid expression in kidney of an individual with the rare blood group A1 Le(a−b+) p phenotype: absence of blood group structures based on the globoseries

  • Papers
  • Published:
Glycoconjugate Journal Aims and scope Submit manuscript

Abstract

Total neutral glycolipid fractions were isolated from kidney and ureter tissue obtained at autopsy of an individual of the rare blood group A1 Le(a−b+) p. The amount of glycolipids isolated were 3.7 and 2.5 mg g−1 dry tissue weight for the kidney and ureter tissue, which is in the range of reference blood group P kidneys. Part of the kidney glycolipid fraction was subfractionated by HPLC. Glycolipid compounds were structurally characterized by thin-layer chromatography (chemical detection and immunostaining with monoclonal antibodies), proton NMR spectroscopy and mass spectrometry. Globotriaosyl- and globotetraosyl-ceramides, which are the major compounds in kidneys of P individuals, were absent in the p kidney, and a comparatively increased amount of monoglycosyland lactosylceramides was found. A shift to longer fatty acyl chains in the ceramide part of lactosylceramides was noted. Elongated globoseries compounds with five to seven sugar residues, including the blood group A type 4 chain structure, were lacking. A slight increase in neolactotetraosyl- and blood group X pentaglycosyl-ceramides was noticed. The study confirms an enzymatic block in the conversion of lactosylceramide to elongated globoseries compounds in the kidney tissue similar to that of erythrocytes of p individuals.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Naiki M, Marcus DM (1974)Biochem Biophys Res Commun 60: 1105–11.

    Google Scholar 

  2. Naiki M, Fong J, Ledeen R, Marcus DM (1975)Biochemistry 14: 4831–37.

    Google Scholar 

  3. Mollison PL, Engelfriet CP, Contreras M (1987) InBlood Transfusion in Clinical Medicine, 8th edition p. 313, Oxford: Blackwell Scientific Publications.

    Google Scholar 

  4. Cedergren B (1973)Hereditas 73: 27–30.

    Google Scholar 

  5. Marcus DM, Naiki M, Kundu SK (1976)Proc Natl Acad Sci USA 73: 3263–67.

    Google Scholar 

  6. Koscielak J, Miller-Podraza H, Krauze R, Cedergren B (1976)FEBS Lett 66: 250–53.

    Google Scholar 

  7. Breimer ME, Cedergren B, Karlsson K-A, Nilson K, Samuelsson BE (1980)FEBS Lett 118: 209–11.

    Google Scholar 

  8. Hattori H, Uemura K, Ogata H, Katsuyama T, Taketomi T, Kanfer JN (1987)Cancer Res 47: 1968–72.

    Google Scholar 

  9. Kannagi R, Levine P, Watanabe K, Hakomori S (1982)Cancer Res 42: 5249–54.

    Google Scholar 

  10. Fellous M, Gerbal A, Nobillot G, Weils J (1977)Vox Sang 32: 262–68.

    Google Scholar 

  11. Lindström K, von dem Borne AEGKr, Breimer ME, Cedergren B, Okubo Y, Rydberg L, Teneberg S, Samuelsson BE (1992)Glycoconjugate J 9: 325–29.

    Google Scholar 

  12. Holgersson J, Clausen H, Hakomori S, Samuelsson BE, Breimer ME (1990)J Biol Chem 265: 20790–98.

    Google Scholar 

  13. Ulfvin A, Bäcker AE, Clausen H, Hakomori S, Rydberg L, Samuelsson BE, Breimer ME (1993)Kidney Int 44: 1289–97.

    Google Scholar 

  14. Holgersson J, Jovall PÅ, Samuelsson BE, Breimer ME (1991)Glycoconjugate J 8: 424–33.

    Google Scholar 

  15. Karlsson K-A (1987)Methods in Enzymology (Ginsburg V, ed.) vol 138, pp. 212–220. London: Academic Press.

    Google Scholar 

  16. Breimer ME, Hansson GC, Karlsson K-A, Larson G, Leffler H, Pascher I, Pimlott W, Samuelsson BE (1980)Adv Mass Spectrum 8: 1097–108.

    Google Scholar 

  17. von dem Borne AEGKr, Bos MJE, Joustra-Maas N, Tromp JF, van Wijngaarden-du-Bois R, Tetteroo PAT (1986)Brit J Haematol 63: 35–46.

    Google Scholar 

  18. Proceedings of the Second Workshop and Symposium on Monoclonal Antibodies against Red Cells and related Antigens (1990)J Immunogenet 17: 350.

    Google Scholar 

  19. Le Pendu J, Lambert F, Samuelsson B, Breimer ME, Seitz RC, Urdaniz MP, Suesa N, Ratcliffe M, Francois A, Poschmann A, Vinas J, Oriol R (1986)Glycoconjugate J 3: 255–71.

    Google Scholar 

  20. Clausen H, McKibbin JM, Hakomori S (1985)Biochemistry 24: 6190–94.

    Google Scholar 

  21. Clausen H, Levery SB, Nudelman S, Tsuchiya A, Hakomori S (1985)Proc Natl Acad Sci USA 82: 1199–203.

    Google Scholar 

  22. Clausen H, Levery SB, Nudelman E, Baldwin M, Hakomori S (1986)Biochemistry 25: 7075–85.

    Google Scholar 

  23. Abe K, McKibbin JM, Hakomori S (1983)J Biol Chem 258: 11793–97.

    Google Scholar 

  24. Dabrowski J, Hanfland P, Egge H (1980)Biochemistry 19: 5652–58.

    Google Scholar 

  25. Breimer ME, Karlsson K-A, Samuelsson BE (1981)J Biol Chem 256: 3810–16.

    Google Scholar 

  26. Levery SB, Nudelman ED, Andersen NH, Hakomori S (1986)Carbohydrate Res 151: 311–28.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Abbreviations: for blood group glycolipid antigens the short hand designation stands for: blood group — number of sugar residues — type of carbohydrate chain. Thus A-7-4 means a blood group A heptaglycoconjugate on a type 4 chain. The sugar types are abbreviated for mass spectrometry to Hex for hexose, HexNAc forN-acetylhexosamine and dHex for deoxyhexose. HPLC, high-performance liquid chromatography; HPTLC, high performance thin layer chromatography; EI, electron impact ionisation; LSI, liquid secondary ion; MS, mass spectrometry; NMR, nuclear magnetic resonance.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lindström, K., Jovall, PÅ., Ghardashkani, S. et al. Blood group glycosphingolipid expression in kidney of an individual with the rare blood group A1 Le(a−b+) p phenotype: absence of blood group structures based on the globoseries. Glycoconjugate J 13, 307–313 (1996). https://doi.org/10.1007/BF00731505

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00731505

Keywords

Navigation