Serveur d'exploration sur le patient édenté (maquette)

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Early molecular assessment of osseointegration in humans.

Identifieur interne : 000618 ( PubMed/Checkpoint ); précédent : 000617; suivant : 000619

Early molecular assessment of osseointegration in humans.

Auteurs : Ghadeer N. Thalji [États-Unis] ; Salvador Nares ; Lyndon F. Cooper

Source :

RBID : pubmed:24118318

Descripteurs français

English descriptors

Abstract

To determine the early temporal-wide genome transcription regulation by the surface topography at the bone-implant interface of implants bearing microroughened or superimposed nanosurface topology.

DOI: 10.1111/clr.12266
PubMed: 24118318


Affiliations:


Links toward previous steps (curation, corpus...)


Links to Exploration step

pubmed:24118318

Le document en format XML

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<title xml:lang="en">Early molecular assessment of osseointegration in humans.</title>
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<name sortKey="Thalji, Ghadeer N" sort="Thalji, Ghadeer N" uniqKey="Thalji G" first="Ghadeer N" last="Thalji">Ghadeer N. Thalji</name>
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<nlm:affiliation>Department of Prosthodontics, University of Iowa, Iowa City, IA, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Prosthodontics, University of Iowa, Iowa City, IA</wicri:regionArea>
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<name sortKey="Nares, Salvador" sort="Nares, Salvador" uniqKey="Nares S" first="Salvador" last="Nares">Salvador Nares</name>
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<name sortKey="Cooper, Lyndon F" sort="Cooper, Lyndon F" uniqKey="Cooper L" first="Lyndon F" last="Cooper">Lyndon F. Cooper</name>
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<title level="j">Clinical oral implants research</title>
<idno type="eISSN">1600-0501</idno>
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<term>Antigens, CD20 (genetics)</term>
<term>Biomarkers (analysis)</term>
<term>Bone-Implant Interface (anatomy & histology)</term>
<term>Chemokines, CC (genetics)</term>
<term>Collagen (genetics)</term>
<term>Dental Implants</term>
<term>Dental Materials (chemistry)</term>
<term>Dental Prosthesis Design</term>
<term>Extracellular Matrix (genetics)</term>
<term>Female</term>
<term>Gene Expression Profiling (methods)</term>
<term>Humans</term>
<term>Macrophage Activation (genetics)</term>
<term>Male</term>
<term>Membrane Proteins (genetics)</term>
<term>Middle Aged</term>
<term>Neovascularization, Physiologic (genetics)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Osseointegration (genetics)</term>
<term>Receptors, Immunologic (genetics)</term>
<term>Scavenger Receptors, Class A (genetics)</term>
<term>Surface Properties</term>
<term>Titanium (chemistry)</term>
<term>Transcription, Genetic (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Activation des macrophages (génétique)</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de profil d'expression de gènes ()</term>
<term>Antigènes CD20 (génétique)</term>
<term>Chimiokines CC (génétique)</term>
<term>Collagène (génétique)</term>
<term>Conception de prothèse dentaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Implants dentaires</term>
<term>Interface os-implant (anatomie et histologie)</term>
<term>Marqueurs biologiques (analyse)</term>
<term>Matrice extracellulaire (génétique)</term>
<term>Matériaux dentaires ()</term>
<term>Mâle</term>
<term>Néovascularisation physiologique (génétique)</term>
<term>Ostéo-intégration (génétique)</term>
<term>Propriétés de surface</term>
<term>Protéines de tissu nerveux (génétique)</term>
<term>Protéines membranaires (génétique)</term>
<term>Récepteurs immunologiques (génétique)</term>
<term>Récepteurs éboueurs de classe A (génétique)</term>
<term>Sujet âgé</term>
<term>Systèmes de transport d'acides aminés neutres (génétique)</term>
<term>Titane ()</term>
<term>Transcription génétique (génétique)</term>
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<term>Biomarkers</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Dental Materials</term>
<term>Titanium</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Amino Acid Transport Systems, Neutral</term>
<term>Antigens, CD20</term>
<term>Chemokines, CC</term>
<term>Collagen</term>
<term>Membrane Proteins</term>
<term>Nerve Tissue Proteins</term>
<term>Receptors, Immunologic</term>
<term>Scavenger Receptors, Class A</term>
</keywords>
<keywords scheme="MESH" qualifier="analyse" xml:lang="fr">
<term>Marqueurs biologiques</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomie et histologie" xml:lang="fr">
<term>Interface os-implant</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomy & histology" xml:lang="en">
<term>Bone-Implant Interface</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Extracellular Matrix</term>
<term>Macrophage Activation</term>
<term>Neovascularization, Physiologic</term>
<term>Osseointegration</term>
<term>Transcription, Genetic</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Activation des macrophages</term>
<term>Antigènes CD20</term>
<term>Chimiokines CC</term>
<term>Collagène</term>
<term>Matrice extracellulaire</term>
<term>Néovascularisation physiologique</term>
<term>Ostéo-intégration</term>
<term>Protéines de tissu nerveux</term>
<term>Protéines membranaires</term>
<term>Récepteurs immunologiques</term>
<term>Récepteurs éboueurs de classe A</term>
<term>Systèmes de transport d'acides aminés neutres</term>
<term>Transcription génétique</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Gene Expression Profiling</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Aged</term>
<term>Dental Implants</term>
<term>Dental Prosthesis Design</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Surface Properties</term>
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<term>Adulte d'âge moyen</term>
<term>Analyse de profil d'expression de gènes</term>
<term>Conception de prothèse dentaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Implants dentaires</term>
<term>Matériaux dentaires</term>
<term>Mâle</term>
<term>Propriétés de surface</term>
<term>Sujet âgé</term>
<term>Titane</term>
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<front>
<div type="abstract" xml:lang="en">To determine the early temporal-wide genome transcription regulation by the surface topography at the bone-implant interface of implants bearing microroughened or superimposed nanosurface topology.</div>
</front>
</TEI>
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<PMID Version="1">24118318</PMID>
<DateCompleted>
<Year>2016</Year>
<Month>09</Month>
<Day>13</Day>
</DateCompleted>
<DateRevised>
<Year>2014</Year>
<Month>10</Month>
<Day>04</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1600-0501</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>25</Volume>
<Issue>11</Issue>
<PubDate>
<Year>2014</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>Clinical oral implants research</Title>
<ISOAbbreviation>Clin Oral Implants Res</ISOAbbreviation>
</Journal>
<ArticleTitle>Early molecular assessment of osseointegration in humans.</ArticleTitle>
<Pagination>
<MedlinePgn>1273-85</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/clr.12266</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To determine the early temporal-wide genome transcription regulation by the surface topography at the bone-implant interface of implants bearing microroughened or superimposed nanosurface topology.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">Four commercially pure titanium implants (2.2 × 5.0 mm) with either a moderately roughened surface (TiOblast) or super-imposed nanoscale topography (Osseospeed) were placed (n = 2/surface) in edentulous sites of eleven systemically healthy subjects and subsequently removed after 3 and 7 days. Total RNA was isolated from cells adherent to retrieved implants. A whole-genome microarray using the Affymetrix Human gene 1.1 ST Array was used to describe the gene expression profiles that were differentially regulated by the implant surfaces.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">There were no significant differences when comparing the two implant surfaces at each time point. However, the microarray identified several genes that were differentially regulated at day 7 vs. day 3 for both implant surfaces. Functionally relevant categories related to the extracellular matrix (ECM), collagen fibril organization, and angiogenesis were upregulated at both surfaces (day7 vs. day3). Abundant upregulation of several differential markers of alternative activated macrophages was observed (e.g., MRC1, MSR1, MS4A4A, SLC38A6, and CCL18). The biological processes involved with the inflammatory/immune response gene expression were concomitantly downregulated.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Gene regulation implicating collagen fibrillogenesis and ECM organization as well as the inflammatory/immune responses involving the alternative activated pathway are observed in implant adherent cells at early (3-7 days) after implantation. These gene expression events may indicate a pivotal role of collagen fibrillogenesis as well as immunomodulation in altering bone accrual and biomechanical physical properties of the implant-bone interface.</AbstractText>
<CopyrightInformation>© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Thalji</LastName>
<ForeName>Ghadeer N</ForeName>
<Initials>GN</Initials>
<AffiliationInfo>
<Affiliation>Department of Prosthodontics, University of Iowa, Iowa City, IA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Nares</LastName>
<ForeName>Salvador</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Cooper</LastName>
<ForeName>Lyndon F</ForeName>
<Initials>LF</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
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<DataBankName>GENBANK</DataBankName>
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<AccessionNumber>GSE41446</AccessionNumber>
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<Year>2013</Year>
<Month>09</Month>
<Day>30</Day>
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<Country>Denmark</Country>
<MedlineTA>Clin Oral Implants Res</MedlineTA>
<NlmUniqueID>9105713</NlmUniqueID>
<ISSNLinking>0905-7161</ISSNLinking>
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<NameOfSubstance UI="C495139">MSR1 protein, human</NameOfSubstance>
</Chemical>
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<Keyword MajorTopicYN="N">biomaterials</Keyword>
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