| Project/Area Number |
01570152
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Pathological medical chemistry
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| Research Institution | Niigata University |
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Principal Investigator |
ABE Sachiko Brain Research Institute, Neurochemistry, Assistant, 脳研究所, 助手 (60018603)
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| Co-Investigator(Kenkyū-buntansha) |
WATANABE Yoko College of Biomedical Technology, Assistant Medical Technology, 医療技術短期大学部, 助手 (80018853)
SATAKE Mei Brain Research Institute, Neurochemistry, Professor, 脳研究所, 教授 (70018589)
ARAKI Shigeko Brain Research Institute, Neurochemistry, Assistant, 脳研究所, 助手 (70018604)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1991: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1990: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1989: ¥1,000,000 (Direct Cost: ¥1,000,000)
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| Keywords | Aplysia nervous tissue / immunohistochemistry / phosphonoglycosphingolipid / nerve bundle-specific / pyruvylated galactose / nerve bundle-specific |
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| Research Abstract |
We isolated four phosphonoglycosphingolipids, designated FGL-IIa, FGL-IIb, FGL-V and F-21, from the nervous system of A. kurodai by Iatrobeads column chromatography using three solvent systems and elucidated their complete structures, respectively. Pyruvic acid attached as a ketal to O-3 and O-4 of the terminal galactose of the oligosaccharide chain in FGL-IIa, FGL-IIb and FGL-V. F-21 has 3-O-methylgalactose as its non-reducing end sugar and one of its three 2-aminoethylphosphonate molecules is linked to C_6 of N-acetylgalactosamine.
We raised a polyclonal antibody against FGL-IIb and examined the antigens that reacted with this anti-FGL-IIb antiserum by TLC-immunostaining. The antiserum reacted with FGL-IIb, FGL-I, FGL-IIa, FGL-V and F-9, which were identified in ganglia and nerve fibers on TLC plates. When cryostat and paraffin sections of the nervous tissue and skin of Aplysia were treated with the antiserum, only nerve bundles were distinctly stained. From histochemical findings in cryostat sections pretreated with chloroform-methanol (2 : 1, v/v) and from results by Western blot analysis of the nervous system, the staining was concluded to be due to glycolipid antigens. In nerve bundles disintegrated with Disperse, periaxonal materials or small periaxonal cells were stained but axons were not stained. This peculiar location of these glycolipids suggests roles of these glycolipids in neurite outgrowth and fasciculation.
In primary cultures of Aplysia neurons and in clonal cultures of neuronal cell lines, we have not yet obtained results that indicate whether or not the new glycolipid family has these proposed neurobiological functions.
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