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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1998-10-19
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pubmed:abstractText |
Biomaterial-mediated complement activation repeatedly has been invoked as a trigger of phagocyte reactions and inflammation. However, a direct correlation between complement activation and inflammatory responses to biomaterial surfaces has yet to be established. Using an animal implantation model and gold surfaces bearing various thiol-linked functionalities, we investigated the potency of different surface groups in prompting complement activation in vitro and surface-mediated accumulation of inflammatory cells in vivo. Among the surfaces tested, mercaptoglycerol- and mercaptoethanol-bearing surfaces engendered the strongest inflammatory responses, as reflected by the accumulation of large numbers of adherent neutrophils and monocytes/macrophages. In contrast, L-cysteine-coated surfaces caused only minor inflammatory responses, and both glutathione-modified and untreated gold implants attracted minimal numbers of inflammatory cells. The accumulation of inflammatory cells on mercaptoglycerol surfaces appears to arise from surface-mediated complement activation because complement-depleted animals failed to exhibit inflammatory responses to mercaptoglycerol-modified implants. Furthermore, there is a close relationship between surface-mediated complement activation (as measured by in vitro iC3b/C5b-9 generation and C3 deposition) and in vivo inflammatory responses. At least in this animal model and with these model surfaces, our results indicate that surface-mediated complement activation can be responsible for the subsequent accumulation of inflammatory cells on implant surfaces.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Cobra Venoms,
http://linkedlifedata.com/resource/pubmed/chemical/Cysteine,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Glycerol,
http://linkedlifedata.com/resource/pubmed/chemical/Gold,
http://linkedlifedata.com/resource/pubmed/chemical/Mercaptoethanol,
http://linkedlifedata.com/resource/pubmed/chemical/cobra venom factor,
http://linkedlifedata.com/resource/pubmed/chemical/thioglycerol
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0021-9304
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
333-40
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9638539-Animals,
pubmed-meshheading:9638539-Biocompatible Materials,
pubmed-meshheading:9638539-Cobra Venoms,
pubmed-meshheading:9638539-Complement Activation,
pubmed-meshheading:9638539-Complement Pathway, Alternative,
pubmed-meshheading:9638539-Cysteine,
pubmed-meshheading:9638539-Foreign-Body Reaction,
pubmed-meshheading:9638539-Glutathione,
pubmed-meshheading:9638539-Glycerol,
pubmed-meshheading:9638539-Gold,
pubmed-meshheading:9638539-Inflammation,
pubmed-meshheading:9638539-Male,
pubmed-meshheading:9638539-Materials Testing,
pubmed-meshheading:9638539-Mercaptoethanol,
pubmed-meshheading:9638539-Mice,
pubmed-meshheading:9638539-Phagocytes,
pubmed-meshheading:9638539-Prostheses and Implants
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pubmed:year |
1998
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pubmed:articleTitle |
Complement activation and inflammation triggered by model biomaterial surfaces.
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pubmed:affiliation |
Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030-3498, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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