Characterization of Phosphonoglycosphingolipids Containing Pyruvate: Localization in Aplysia Nerve Bundles
A phosphonoglycosphingolipid, designated as FGL-IIb, was first identified in nerve fibers of Aplysia kurodai by two-dimensional TLC (Abe, S. et al. (1986) BiomecL Res. 7, 47–51), and its chemical structure has been determined to be 3, 4–0-(l-carboxyethylidene)]Galβ1↑ 3GalNAc α 1→3(Fuc α1→2)(2-aminoe...
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Veröffentlicht in: | Journal of biochemistry (Tokyo) 1989-12, Vol.106 (6), p.972-976 |
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Zusammenfassung: | A phosphonoglycosphingolipid, designated as FGL-IIb, was first identified in nerve fibers of Aplysia kurodai by two-dimensional TLC (Abe, S. et al. (1986) BiomecL Res. 7, 47–51), and its chemical structure has been determined to be 3, 4–0-(l-carboxyethylidene)]Galβ1↑ 3GalNAc α 1→3(Fuc α1→2)(2-aminoethylphosphonyl→ 6)Gal β1→4Glc β1→ lceramide (Araki, S. et al., submitted). Cryostat and paraffin sections of the nervous tissue and skin of Aplysia were examined immunohistochemically with antiserum against FGL-IIb. With this antiserum, only nerve bundles were stained distinctly: nerve cells in ganglia and in subcutaneous and muscular tissues and other cell elements were not stained. From histochemical findings in cryostat sections pretreated with chloroform methanol (2: 1, v/ v) and from the results of Western blot analysis of the nervous tissue, the staining was concluded to be due to glycolipid antigens. The antiserum reacted with FGL-IIb and other phosphonoglycosphingolipids named FGL-I, FGL-IIa, FGL-V, and F-9 on TLC plates. This reactivity of FGL-IIb was abolished by mild acid-methanol treatment, and the lost reactivity was recovered by alkaline hydrolysis. These findings suggest that the free carboxyl group of the pyruvic acid of FGL-IIb is essential for the immunological reaction and that all the glycolipids listed above have the same epitope as that of FGL-IIb. Immunohistochemical findings indicated that these glycolipids including FGL-IIb are localized specifically in nerve bundles of Aplysia. |
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ISSN: | 0021-924X 1756-2651 |
DOI: | 10.1093/oxfordjournals.jbchem.a122984 |