| Project/Area Number |
03454433
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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 |
Functional basic dentistry
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| Research Institution | KYUSHU UNIVERSITY |
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Principal Investigator |
YAMAMOTO Kenji KYUSHU UNIVERSITY DENTAL PHARMACOLOGY PROFESSOR, 歯学部, 教授 (40091326)
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| Co-Investigator(Kenkyū-buntansha) |
EZAKI Mitsue KYUSHU UNIVERSITY DENTAL PHARMACOLOGY, INSTRUCTOR, 歯学部, 助手 (30223647)
KAMATA Osamu KYUSHU UNIVERSITY DENTAL PHARMACOLOGY, ASSOCIATE PROFESSOR, 歯学部, 助教授 (80037580)
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| Project Period (FY) |
1991 – 1992
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| Project Status |
Completed (Fiscal Year 1992)
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| Budget Amount *help |
¥6,700,000 (Direct Cost: ¥6,700,000)
Fiscal Year 1992: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1991: ¥6,300,000 (Direct Cost: ¥6,300,000)
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| Keywords | OSTEOCLAST / BONE RESORPTION / LYSOSOMAL MEMBRANE PROTEIN / CATHEPSIN B / CATHEPSIN L / CATHEPSIN D / リソゾ-ム膜タンバン質 |
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| Research Abstract |
Osteoclastic bone resorption is associated with both the removal of bone mineral and the degradation of bone organic matrix through hydrolytic enzymes secreted by the cells. The present study was designed to investigate the role of lysosomal membrane proteins in the formation of acidic conditions of the bone resorption lacuna and the functional importance of lysosomal proteinases in the bone resorbing process. For this purpose, the levels and localizations of a major 107 kDa lysosomal membrane glycoprotein (designated as LGP107) and lysosomal proteinases (cathepsins B,L and D) in rat osteoclasts were determined by immunocytochemical techniques using antibodies specific for each enzyme. LGP107 was exclusively confined to the apical plasma membrane at the ruffled border of active osteoclasts, where the cells were contact with the bone surface. The ruffled border membrane detached from the bone surface showed a marked decrease in the extent of the immunolabeling. Since LGP107 is highly sialylated and has the very low pI, the protein is likely to contribute to the formation and maintenance of the bone resorption lacuna. Extracellular localization of cathepsins B and L, lysosomal cysteine proteinases, was clearly shown along the bone resorption lacuna and the intracellular immunoreactivity of both cathepsins was weak compared with that of cathepsin D,a lysosomal aspartic proteinase. Cathepsin D was intensely observed in the granules and vacuoles of the osteoclasts, but its extracellular localization was either negligible or not detected along the bone resorption lacuna. These results suggest that these proteinases have their shares of the degradation of the bone matrix.
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