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PMID: 3689344 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The sialic acid residue of exogenous GM1 ganglioside is recycled for biosynthesis of sialoglycoconjugates in rat liver.

The Biochemical journal ·Vol. 247 ·No. 1 ·1987-10-01 ·Pages 157-64

Ghidoni R, Trinchera M, Sonnino S, Chigorno V, Tettamanti G

Abstract

In order to assess metabolic recycling of sialic acid, GM1 ganglioside [nomenclature of Svennerholm (1964) J. Lipid. Res. 5, 145-155; IUPAC-IUB Recommendations (1977) Lipids 12, 455-468], 14C-radiolabelled at the acetyl group of sialic acid, was intravenously injected into Wistar rats, and the presence of radioactive sialic acid in liver sialoglycolipids (gangliosides) and sialoglycoproteins was ascertained. A time-course study (20 min-72 h) showed that the radioactivity present in the liver distributed in the following fractions, with reciprocal proportion varying with time: the protein (glycoprotein) fraction, the ganglioside fraction and the diffusible fraction, which contained low-Mr compounds, including sialic acid. Ganglioside-linked radioactivity gradually decreased with time; protein-linked radioactivity appeared soon after injection (20 min), reached a maximum around 20 h, then slowly diminished; diffusible radioactivity provided a sharp peak at 4 h, then rapidly decreased till disappearing after 40 h. The behaviour of bound radioactivity in the individual liver gangliosides was as follows: (a) rapid diminution with time in GM1, although with a lower rate at the longer times after injection; (b) early appearance (20 min) with a peak at 1 h, followed by continuous diminution, in GM2; (c) early appearance (20 min), peak at 1 h, diminution till 4 h, followed by a plateau, in GM3; (d) appearance at 60 min, maximum around 40 h and slow diminution thereafter, in GD1a, GD1b and GT1b. A detailed study, accomplished at 40 h after injection, demonstrated that almost all radioactivity present in the protein fraction was released by mild acid treatment and recovered in purified sialic acid; most of radioactive glycoprotein-bound sialic acid was releasable by sialidase action. In addition, the radioactivity present in the different gangliosides was exclusively carried by sialic acid and present in both sialidase-resistant and sialidase-labile residues. Only in the case of GD1a was the specific radioactivity of sialidase-resistant sialic acid superior to that of sialidase-releasable sialic acid. The results obtained lead to the following conclusions: (a) radioactive GM3 and GM2 were produced by degradation of GM1 taken up; GM3 originated partly by a process of neosynthesis; (b) radioactive GM1 consisted in part of residual exogenous GM1 and in part of a neosynthetized product; (c) radioactive GD1a originated in part by direct sialylation of GM1 taken up and in part by a neosynthetic process; (d) radioactive GD1b and GT1b resulted only from neosynthesis.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Animals Carbon Radioisotopes Chromatography, Thin Layer G(M1) Ganglioside/metabolism Liver/metabolism Male Models, Biological N-Acetylneuraminic Acid Neuraminidase Rats Rats, Inbred Strains Sialic Acids/metabolism Sialoglycoproteins/biosynthesis
Chemicals
Carbon Radioisotopes Sialic Acids Sialoglycoproteins G(M1) Ganglioside Neuraminidase N-Acetylneuraminic Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ghidoni R
Department of Medical Chemistry and Biochemistry, University of Milan, Italy.
Trinchera M
Sonnino S
Chigorno V
Tettamanti G
References (25)
25 references, click to expand
  1. A new procedure for the extraction, purification and fractionation of brain gangliosides.
    Biochim Biophys Acta. 1973 Jan 19;296(1):160-70 PMID: 4693502
  2. Ganglioside GM1 metabolism in living human fibroblasts with beta-galactosidase deficiency.
    Hum Genet. 1986 May;73(1):35-8 PMID: 3086209
  3. "Salla disease": a new lysosomal storage disorder.
    Arch Neurol. 1979 Feb;36(2):88-94 PMID: 420628
  4. Metabolism of N-acetylneuraminic acid in mammals: isolation and characterization of CMP-N-acetylneuraminic acid.
    Biochemistry. 1979 May 15;18(10):2086-92 PMID: 435467
  5. Isolation and characterization of a trisialoganglioside from mouse brain, containing 9-O-acetyl-N-acetylneuraminic acid.
    J Biol Chem. 1980 Jul 25;255(14):6990-5 PMID: 7391062
  6. Turnover of free sialic acid, CMP-sialic acid, and bound sialic acid in rat brain.
    J Neurochem. 1981 Apr;36(4):1492-9 PMID: 7264646
  7. Studies on the cell association of exogenously added sialo-glycolipids.
    Hoppe Seylers Z Physiol Chem. 1982 Mar;363(3):263-72 PMID: 7076127
  8. Defective cystine exodus from isolated lysosome-rich fractions of cystinotic leucocytes.
    J Biol Chem. 1982 Aug 25;257(16):9570-5 PMID: 7107582
  9. Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblings.
    Eur J Pediatr. 1982 Oct;139(2):142-7 PMID: 7151835
  10. Free N-acetylneuraminic acid in tissues in Salla disease and the enzymes involved in its metabolism.
    Eur J Biochem. 1983 Jan 17;130(1):39-45 PMID: 6297896
  11. Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile type.
    Pediatrics. 1983 Oct;72(4):441-9 PMID: 6889058
  12. Occurrence of glycosylation and deglycosylation of exogenously administered ganglioside GM1 in mouse liver.
    Biochem J. 1983 Aug 1;213(2):321-9 PMID: 6615438
  13. Incorporation of ganglioside analogues into fibroblast cell membranes. A spin-label study.
    Biochemistry. 1983 Oct 11;22(21):5041-8 PMID: 6315058
  14. Studies of lysosomal sialic acid metabolism: retention of sialic acid by Salla disease lysosomes.
    Biochem Biophys Res Commun. 1986 May 29;137(1):175-81 PMID: 3718508
  15. Infantile type of sialic acid storage disease with sialuria.
    Clin Genet. 1986 May;29(5):417-24 PMID: 3742847
  16. N-acetylneuraminic acid accumulation in a buoyant lysosomal fraction of cultured fibroblasts from patients with infantile generalized N-acetylneuraminic acid storage disease.
    Biochem Biophys Res Commun. 1986 Sep 14;139(2):838-44 PMID: 2945557
  17. Incorporation and metabolism of exogenous GM1 ganglioside in rat liver.
    Biochem J. 1986 Jul 1;237(1):147-55 PMID: 3800874
  18. The thiobarbituric acid assay of sialic acids.
    J Biol Chem. 1959 Aug;234(8):1971-5 PMID: 13672998
  19. THE GANGLIOSIDES.
    J Lipid Res. 1964 Apr;5:145-55 PMID: 14174000
  20. Synthesis of N-acetylneuraminic acid and of CMP-N-acetylneuraminic acid in the rat liver cell.
    Biochem J. 1983 Oct 15;216(1):87-92 PMID: 6651781
  21. Cytosolic gangliosides of rat brain: their fractionation into protein-bound complexes of different ganglioside compositions.
    J Neurosci Res. 1984;12(2-3):193-204 PMID: 6502749
  22. Incorporation and metabolism of ganglioside GM2 in skin fibroblasts from normal and GM2 gangliosidosis subjects.
    Eur J Biochem. 1985 Jun 3;149(2):247-55 PMID: 3922757
  23. Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism.
    Science. 1985 Jun 14;228(4705):1319-21 PMID: 4001945
  24. Defective sialic acid egress from isolated fibroblast lysosomes of patients with Salla disease.
    Science. 1986 May 9;232(4751):759-62 PMID: 3961501
  25. Characterization of sialic acids.
    Methods Enzymol. 1978;50:64-89 PMID: 207950
Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1987-10-01
Pages
157-64
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1148383
Subset
IM
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