| Project/Area Number |
07670703
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neurology
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| Research Institution | Tokyo Medical and Dental University |
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Principal Investigator |
KANDA Takashi TOKYO MEDICAL & DENTAL UNIVERSITY,NEUROLOGY,Assistant Professor, 医学部, 助手 (40204797)
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| Project Period (FY) |
1995 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1997: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1996: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1995: ¥700,000 (Direct Cost: ¥700,000)
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| Keywords | Blood-Nerve Barrier / Endothermal Cell / Cell Culture / Ganglioside / Neuropathy / Cell Biology / ニューロパタ- / Endothelial cell / blood-nerve barrier / ganglioside / Antibody / neuropathy / glycolipid / glucose transporten I / 血液神経閉門 / 血管内皮細胞 / 細胞接着因子 |
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| Research Abstract |
Penetration of immunoglobulins and/or migration of activated lumphocytes into peripheral nervous system (PNS) parenchyma are the initial key steps to develop immunological disorders of PNS including Guillain-Barre syndrome, IgM neuropathy and chronic inflammatory demyelinating polyradiculoneuropathy. Hence, it is important to know the cellular property of endothelial cells of endoneurial tissue origin (PnMEC) because these cells constitute the bulk of the blood-nerve barrier (BNB). For this purpose we developed a method to isolate and culture pure populations of PnMECs from bovine cauda euina. PnMECs were identified by their cobblestone appearance, immunoreactivity against Factor VIII/von Willebrand factor (vWF) antigen, and positive uptake of Dil-Ac-LDL.The glucose transporter type 1 (GLUT1) expression of these cells was rapidly down-regulated in vitro. Other thatn GM3 (NeuAc) and GM3 (NeuGc) as major glycosphingolipids, PnMECs comprise GM1, GD1a, GD1b and GT1b, which are shared by PNS parenchyma, and sialyl lactosaminyl paragloboside (SLPG) as minor species. Because bovine PnMECs proliferate rapidly and a large mass of cells could be obtained, this method should contribute to the biochemical analysis of surface molecules in PnMECs that might play a key role in the formation of BNB as well as in pathological conditions involving the PNS.
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