| Project/Area Number |
06454266
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Gastroenterology
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| Research Institution | Juntendo University School of Medicine |
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Principal Investigator |
SATO Nobuhiro Juntendo Univ.School of Medicine, Professor, 医学部, 教授 (90028358)
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| Co-Investigator(Kenkyū-buntansha) |
MAEHIRO Kohei Juntendo Univ.School of Medicine, 医学部, 助手 (30238878)
YAMAGUCHI Yasushi Juntendo Univ.School of Medicine, 医学部, 助手 (70241015)
KITAMURA Tsuneo Juntendo Univ.School of Medicine, 医学部, 助手 (20231285)
WATANABE Sumio Juntendo Univ.School of Medicine, Assistant Professor, 医学部, 助教授 (20138225)
横井 幸男 順天堂大学, 医学部, 講師 (20150633)
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| Project Period (FY) |
1994 – 1995
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| Project Status |
Completed (Fiscal Year 1995)
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| Budget Amount *help |
¥7,300,000 (Direct Cost: ¥7,300,000)
Fiscal Year 1995: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1994: ¥6,000,000 (Direct Cost: ¥6,000,000)
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| Keywords | gastric ulcer / growth factor / cytoskeleton / migration / proliferation / wound healing / culture cell / gastric ulcer / growth factor / cytoskeleton / migration / proliferation / wound healing / culture cell / gastric ulcer 男性度 / growth factor 増殖因子 / cytoskeleton 細胞骨性 / migration 細胞遊走 / proliferation 細胞増殖 / wound healing 損傷性対 / culture cell 培養細胞 / 胃粘膜細胞 / 損傷修復モデル / 細胞外基質 / 受容体 |
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| Research Abstract |
The precise cellular mechanism of growth factors on gastric wound repair is still controversial. We investigated the role of growth factors on gastric mucosal restoration using primary cultured rabbit gastric epithelial cells and fibroblasts. Isolated rabbit gastric epitherial cells and fibroblasts were prepared from identical rabbit and cultured in F-12 medium. Inoculated epithelial cells (92% mucous cell) formed complete monolayr in 48h and fibroblasts formed complete monolayr in 4 weeks. A wound with cell-freearea of constant size was created by mechanical cell denudation using rotating silicon tip. The restoration process was monitored by measuring wound size every 12 h using a time-lapse video system. The proliferative cells were detected by serial staining for BrdU.Effects of EGF, Insulin, bFGF, HGF, TGFalpha and PDGF were assessed. EGF, Insulin, HGF, TGFalpha and PDGF accelerated the gastric epithelial restoration with the promotion of cell migration and proliferation. bFGF and PDGF accelerated the gastric mesenchymal restoration. The difference of target cells of growth factor might modulate gastric ulcer healing and the integrity of growth factor network during the process of ulcer healing is essential for high quality ulcer healing.
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