Source:http://linkedlifedata.com/resource/pubmed/id/10520966
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
1999-10-28
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pubmed:abstractText |
Bone resorption is regulated by the cytokines within marrow cells that mediate osteoclast formation and activation. IL-1 and TNF induce bone resorption by stimulating the production of osteoclast-like multinucleated cells and by increasing the bone-resorbing activity of formed osteoclasts. This study was designed to detect IL-1 and TNF in osteoclasts in vitro and to determine whether these cytokines up-regulate osteoclast differentiation and bone resorption. The production of IL-1 alpha, -beta, and TNF alpha, beta in osteoclasts was examined immunohistochemically and by in situ hybridization. In the co-culture of C57BL/6N mouse bone marrow and MC3T3-G2/PA6 cells, a colony of osteoclasts formed, and IL-1 alpha and TNF alpha were detected. However, IL-1 beta and TNF beta were not detected. To investigate the role of IL-1 alpha and TNF alpha from osteoclasts, we enumerated TRAP-positive cells and measured the resorption pit areas in the presence of antibodies against IL-1 alpha and TNF alpha. The addition of antibodies against IL-1 alpha and TNF alpha to the co-culture system decreased the number of TRAP-positive colonies at seven days after incubation (anti-IL-1 alpha, 25.0 +/- 2.3%; anti-TNF alpha, 41.7 +/- 3.7%; anti-IL-1 alpha + anti-TNF alpha, 40.5 +/- 1.3%; and control, 100%), and the ratio of mononuclear to multinuclear cells had changed (anti-IL-1 alpha, 90:10; anti-TNF alpha, 75:25; anti-IL-1 alpha+ anti-TNF alpha, 88:12; and control, 60:40). The total pit areas per dentin slice also decreased with the addition of antibodies (anti-IL-1 alpha, 28,828; anti-TNF alpha, 49,249; anti-IL-1 alpha + anti-TNF alpha, 30,685; and control, 303,139 mm2). These results suggest that local production of IL-1 alpha and TNF alpha by osteoclasts is an important mechanism for regulating the osteoclast differentiation and bone resorptive process.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
D
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acid Phosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/tartrate-resistant acid phosphatase
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0022-0345
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
78
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1617-23
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10520966-Acid Phosphatase,
pubmed-meshheading:10520966-Animals,
pubmed-meshheading:10520966-Biological Markers,
pubmed-meshheading:10520966-Bone Marrow Cells,
pubmed-meshheading:10520966-Bone Resorption,
pubmed-meshheading:10520966-Cell Differentiation,
pubmed-meshheading:10520966-Cell Line,
pubmed-meshheading:10520966-Cells, Cultured,
pubmed-meshheading:10520966-Coculture Techniques,
pubmed-meshheading:10520966-Female,
pubmed-meshheading:10520966-Immunohistochemistry,
pubmed-meshheading:10520966-In Situ Hybridization,
pubmed-meshheading:10520966-Interleukin-1,
pubmed-meshheading:10520966-Isoenzymes,
pubmed-meshheading:10520966-Mice,
pubmed-meshheading:10520966-Mice, Inbred C57BL,
pubmed-meshheading:10520966-Osteoclasts,
pubmed-meshheading:10520966-Tumor Necrosis Factor-alpha,
pubmed-meshheading:10520966-Up-Regulation
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pubmed:year |
1999
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pubmed:articleTitle |
Autocrine regulation of osteoclast formation and bone resorption by IL-1 alpha and TNF alpha.
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pubmed:affiliation |
Department of Operative Dentistry and Endodontics, Kanagawa Dental College, Yokosuka, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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