| Project/Area Number |
05670659
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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 |
Pediatrics
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| Research Institution | National Institute of Neuroscience, NCNP |
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Principal Investigator |
MIZUGUCHI Masashi Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, NCNP Section Chief, 神経研究所・疾病研究第2部, 室長 (20209753)
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| Co-Investigator(Kenkyū-buntansha) |
YAMADA Mitsunori Department of Pathology, Brain Research Institute, Niigata University Assistant, 脳研究所・実験神経病理学部門, 助手 (30240039)
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| Project Period (FY) |
1993 – 1994
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| Project Status |
Completed (Fiscal Year 1994)
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| Budget Amount *help |
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1994: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1993: ¥1,300,000 (Direct Cost: ¥1,300,000)
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| Keywords | Second messenger / Inositol 1,4,5-trisphosphate / Cyclic ADP-ribose / CD38 / Calcium ion / Immunohistochemistry / Central nervous System / イノシトールリン脂質 / 細胞内情報伝達 |
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| Research Abstract |
A.Studies on the phosphoinositide-mediated system.
Developmental changes of inositol 1,4,5-trisphosphate 3-kinase (IP3K) were investigated in rat cerebellum by immunoelectron microscopy. An important role of this system during development was suggested by the high expression of IP3K observed on structures having special developmental significance, such as the synapses between the prarllel fibers and the proximal dendrites of Purkinje cells.
B.Studies on the cyclic ADP-ribose (cADPR) -mediated system.
The expression in brain of CD38 antigen, which is involved in both the formation and hydrolysis of cADPR,was investigated with polyclonal antibodies raised against synthetic CD38 peptide fragments. Using these antibodies in addition to monoclonals, the presence of CD38 in brain was demonstrated by both immunochemical and immunohistochemical methods.
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