Novel Implant Coating Agent Promotes Gene Expression of Osteogenic Markers in Rats during Early Osseointegration
Identifieur interne : 003130 ( Main/Exploration ); précédent : 003129; suivant : 003131Novel Implant Coating Agent Promotes Gene Expression of Osteogenic Markers in Rats during Early Osseointegration
Auteurs : Kostas Bougas [Suède] ; Ryo Jimbo [Suède] ; Ying Xue [Norvège] ; Kamal Mustafa [Norvège] ; Ann Wennerberg [Suède]Source :
- International Journal of Biomaterials [ 1687-8787 ] ; 2012.
Abstract
The aim of this study was to evaluate the early bone response around laminin-1-coated titanium implants. Forty-five rats distributed in three equally sized groups were provided with one control (turned) and one test (laminin-1-coated) implant and were sacrificed after 3, 7, and 21 days. Real-time reverse-transcriptase polymerase chain reaction was performed for osteoblast markers (alkaline phosphatase, runt-related transcription factor 2, osteocalcin, type I collagen, and bone morphogenic protein 2), osteoclast markers (cathepsin K and tartrate-resistant acid phosphatase), inflammation markers (tumor necrosis factor
Url:
DOI: 10.1155/2012/579274
PubMed: 23193408
PubMed Central: 3501934
Affiliations:
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<series><title level="j">International Journal of Biomaterials</title>
<idno type="ISSN">1687-8787</idno>
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<front><div type="abstract" xml:lang="en"><p>The aim of this study was to evaluate the early bone response around laminin-1-coated titanium implants. Forty-five rats distributed in three equally sized groups were provided with one control (turned) and one test (laminin-1-coated) implant and were sacrificed after 3, 7, and 21 days. Real-time reverse-transcriptase polymerase chain reaction was performed for osteoblast markers (alkaline phosphatase, runt-related transcription factor 2, osteocalcin, type I collagen, and bone morphogenic protein 2), osteoclast markers (cathepsin K and tartrate-resistant acid phosphatase), inflammation markers (tumor necrosis factor <italic><italic>α</italic>
</italic>
, interleukin 1<italic><italic>β</italic>
</italic>
and interleukin 10), and integrin <italic><italic>β</italic>
</italic>
1. Bone implant contact (BIC) and bone area (BA) were assessed and compared to the gene expression. After 3 days, the expression of bone markers was higher for the control group. After 7 days, the expression of integrin <italic><italic>β</italic>
</italic>
1 and osteogenic markers was enhanced for the test group, while cathepsin K and inflammation markers were down-regulated. No significant differences in BIC or BA were detected between test and control at any time point. As a conclusion, implant coating with laminin-1 altered gene expression in the bone-implant interface. However, traditional evaluation methods, as histomorphometry, were not adequately sensitive to detect such changes due to the short follow-up time.</p>
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