Serveur d'exploration sur les relations entre la France et l'Australie

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Contributions of adhesive proteins to the cellular and bacterial response to surfaces treated with bioactive polymers: case of poly(sodium styrene sulfonate) grafted titanium surfaces.

Identifieur interne : 002F91 ( Main/Exploration ); précédent : 002F90; suivant : 002F92

Contributions of adhesive proteins to the cellular and bacterial response to surfaces treated with bioactive polymers: case of poly(sodium styrene sulfonate) grafted titanium surfaces.

Auteurs : Helena P. Felgueiras [France] ; Ines Ben Aissa [France] ; Margaret D M. Evans [Australie] ; Véronique Migonney [France]

Source :

RBID : pubmed:26449451

Descripteurs français

English descriptors

Abstract

The research developed on functionalized model or prosthetic surfaces with bioactive polymers has raised the possibility to modulate and/or control the biological in vitro and in vivo responses to synthetic biomaterials. The mechanisms underlying the bioactivity exhibited by sulfonated groups on surfaces involves both selective adsorption and conformational changes of adsorbed proteins. Indeed, surfaces functionalized by grafting poly(sodium styrene sulfonate) [poly(NaSS)] modulate the cellular and bacterial response by inducing specific interactions with fibronectin (Fn). Once implanted, a biomaterial surface is exposed to a milieu of many proteins that compete for the surface which dictates the subsequent biological response. Once understood, this can be controlled by dictating exposure of active binding sites. In this in vitro study, we report the influence of binary mixtures of proteins [albumin (BSA), Fn and collagen type I (Col I)] adsorbed on poly(NaSS) grafted Ti6Al4V on the adhesion and differentiation of MC3T3-E1 osteoblast-like cells and the adhesion and proliferation of Staphylococcus aureus (S. aureus). Outcomes showed that poly(NaSS) stimulated cell spreading, attachment strength, differentiation and mineralization, whatever the nature of protein provided at the interface compared with ungrafted Ti6Al4V (control). While in competition, Fn and Col I were capable of prevailing over BSA. Fn played an important role in the early interactions of the cells with the surface, while Col I was responsible for increased alkaline phosphatase, calcium and phosphate productions associated with differentiation. Poly(NaSS) grafted surfaces decreased the adhesion of S. aureus and the presence of Fn on these chemically altered surfaces increased bacterial resistance ≈70% compared to the ungrafted Ti6Al4V. Overall, our study showed that poly(NaSS) grafted Ti6Al4V selectively adsorbed proteins (particularly Fn) promoting the adhesion and differentiation of osteoblast-like cells while reducing bacterial adhesion to create a bioactive surface with potential for orthopaedic applications.

DOI: 10.1007/s10856-015-5596-y
PubMed: 26449451


Affiliations:


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


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Contributions of adhesive proteins to the cellular and bacterial response to surfaces treated with bioactive polymers: case of poly(sodium styrene sulfonate) grafted titanium surfaces.</title>
<author>
<name sortKey="Felgueiras, Helena P" sort="Felgueiras, Helena P" uniqKey="Felgueiras H" first="Helena P" last="Felgueiras">Helena P. Felgueiras</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<wicri:noRegion>93430, Villetaneuse</wicri:noRegion>
<orgName type="university">Université Paris 13</orgName>
<placeName>
<settlement type="city">Paris</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Aissa, Ines Ben" sort="Aissa, Ines Ben" uniqKey="Aissa I" first="Ines Ben" last="Aissa">Ines Ben Aissa</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<wicri:noRegion>93430, Villetaneuse</wicri:noRegion>
<orgName type="university">Université Paris 13</orgName>
<placeName>
<settlement type="city">Paris</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Evans, Margaret D M" sort="Evans, Margaret D M" uniqKey="Evans M" first="Margaret D M" last="Evans">Margaret D M. Evans</name>
<affiliation wicri:level="1">
<nlm:affiliation>CSIRO Biomedical Materials Program, 11 Julius Avenue, North Ride, Sydney, NSW, 2113, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>CSIRO Biomedical Materials Program, 11 Julius Avenue, North Ride, Sydney, NSW, 2113</wicri:regionArea>
<wicri:noRegion>2113</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Migonney, Veronique" sort="Migonney, Veronique" uniqKey="Migonney V" first="Véronique" last="Migonney">Véronique Migonney</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France. veronique.migonney@univ-paris13.fr.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<wicri:noRegion>93430, Villetaneuse</wicri:noRegion>
<orgName type="university">Université Paris 13</orgName>
<placeName>
<settlement type="city">Paris</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2015">2015</date>
<idno type="RBID">pubmed:26449451</idno>
<idno type="pmid">26449451</idno>
<idno type="doi">10.1007/s10856-015-5596-y</idno>
<idno type="wicri:Area/PubMed/Corpus">002719</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002719</idno>
<idno type="wicri:Area/PubMed/Curation">002650</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">002650</idno>
<idno type="wicri:Area/PubMed/Checkpoint">002650</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">002650</idno>
<idno type="wicri:Area/Ncbi/Merge">002B96</idno>
<idno type="wicri:Area/Ncbi/Curation">002B96</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002B96</idno>
<idno type="wicri:Area/Main/Merge">002F92</idno>
<idno type="wicri:Area/Main/Curation">002F91</idno>
<idno type="wicri:Area/Main/Exploration">002F91</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Contributions of adhesive proteins to the cellular and bacterial response to surfaces treated with bioactive polymers: case of poly(sodium styrene sulfonate) grafted titanium surfaces.</title>
<author>
<name sortKey="Felgueiras, Helena P" sort="Felgueiras, Helena P" uniqKey="Felgueiras H" first="Helena P" last="Felgueiras">Helena P. Felgueiras</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Villetaneuse</settlement>
<settlement type="city">Paris</settlement>
</placeName>
<orgName type="university">Université Paris 13</orgName>
</affiliation>
</author>
<author>
<name sortKey="Aissa, Ines Ben" sort="Aissa, Ines Ben" uniqKey="Aissa I" first="Ines Ben" last="Aissa">Ines Ben Aissa</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<wicri:noRegion>93430, Villetaneuse</wicri:noRegion>
<orgName type="university">Université Paris 13</orgName>
<placeName>
<settlement type="city">Paris</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Evans, Margaret D M" sort="Evans, Margaret D M" uniqKey="Evans M" first="Margaret D M" last="Evans">Margaret D M. Evans</name>
<affiliation wicri:level="1">
<nlm:affiliation>CSIRO Biomedical Materials Program, 11 Julius Avenue, North Ride, Sydney, NSW, 2113, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>CSIRO Biomedical Materials Program, 11 Julius Avenue, North Ride, Sydney, NSW, 2113</wicri:regionArea>
<wicri:noRegion>2113</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Migonney, Veronique" sort="Migonney, Veronique" uniqKey="Migonney V" first="Véronique" last="Migonney">Véronique Migonney</name>
<affiliation wicri:level="4">
<nlm:affiliation>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse, France. veronique.migonney@univ-paris13.fr.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de "Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques" (CSPBAT) - UMR CNRS 7244, Institut Galilée, Université Paris 13, Sorbonne Paris Cité, 99 avenue JB Clément, 93430, Villetaneuse</wicri:regionArea>
<wicri:noRegion>93430, Villetaneuse</wicri:noRegion>
<orgName type="university">Université Paris 13</orgName>
<placeName>
<settlement type="city">Paris</settlement>
<region type="region" nuts="2">Île-de-France</region>
</placeName>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Journal of materials science. Materials in medicine</title>
<idno type="eISSN">1573-4838</idno>
<imprint>
<date when="2015" type="published">2015</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>3T3 Cells</term>
<term>Animals</term>
<term>Bacterial Adhesion</term>
<term>Bacterial Proteins (chemistry)</term>
<term>Cell Differentiation</term>
<term>Cell Proliferation</term>
<term>Mice</term>
<term>Polymers (chemistry)</term>
<term>Protein Binding</term>
<term>Spectroscopy, Fourier Transform Infrared</term>
<term>Staphylococcus aureus (physiology)</term>
<term>Surface Properties</term>
<term>Titanium (chemistry)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adhérence bactérienne</term>
<term>Animaux</term>
<term>Cellules 3T3</term>
<term>Différenciation cellulaire</term>
<term>Liaison aux protéines</term>
<term>Polymères ()</term>
<term>Prolifération cellulaire</term>
<term>Propriétés de surface</term>
<term>Protéines bactériennes ()</term>
<term>Souris</term>
<term>Spectroscopie infrarouge à transformée de Fourier</term>
<term>Staphylococcus aureus (physiologie)</term>
<term>Titane ()</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Bacterial Proteins</term>
<term>Polymers</term>
<term>Titanium</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Staphylococcus aureus</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Staphylococcus aureus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>3T3 Cells</term>
<term>Animals</term>
<term>Bacterial Adhesion</term>
<term>Cell Differentiation</term>
<term>Cell Proliferation</term>
<term>Mice</term>
<term>Protein Binding</term>
<term>Spectroscopy, Fourier Transform Infrared</term>
<term>Surface Properties</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adhérence bactérienne</term>
<term>Animaux</term>
<term>Cellules 3T3</term>
<term>Différenciation cellulaire</term>
<term>Liaison aux protéines</term>
<term>Polymères</term>
<term>Prolifération cellulaire</term>
<term>Propriétés de surface</term>
<term>Protéines bactériennes</term>
<term>Souris</term>
<term>Spectroscopie infrarouge à transformée de Fourier</term>
<term>Titane</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The research developed on functionalized model or prosthetic surfaces with bioactive polymers has raised the possibility to modulate and/or control the biological in vitro and in vivo responses to synthetic biomaterials. The mechanisms underlying the bioactivity exhibited by sulfonated groups on surfaces involves both selective adsorption and conformational changes of adsorbed proteins. Indeed, surfaces functionalized by grafting poly(sodium styrene sulfonate) [poly(NaSS)] modulate the cellular and bacterial response by inducing specific interactions with fibronectin (Fn). Once implanted, a biomaterial surface is exposed to a milieu of many proteins that compete for the surface which dictates the subsequent biological response. Once understood, this can be controlled by dictating exposure of active binding sites. In this in vitro study, we report the influence of binary mixtures of proteins [albumin (BSA), Fn and collagen type I (Col I)] adsorbed on poly(NaSS) grafted Ti6Al4V on the adhesion and differentiation of MC3T3-E1 osteoblast-like cells and the adhesion and proliferation of Staphylococcus aureus (S. aureus). Outcomes showed that poly(NaSS) stimulated cell spreading, attachment strength, differentiation and mineralization, whatever the nature of protein provided at the interface compared with ungrafted Ti6Al4V (control). While in competition, Fn and Col I were capable of prevailing over BSA. Fn played an important role in the early interactions of the cells with the surface, while Col I was responsible for increased alkaline phosphatase, calcium and phosphate productions associated with differentiation. Poly(NaSS) grafted surfaces decreased the adhesion of S. aureus and the presence of Fn on these chemically altered surfaces increased bacterial resistance ≈70% compared to the ungrafted Ti6Al4V. Overall, our study showed that poly(NaSS) grafted Ti6Al4V selectively adsorbed proteins (particularly Fn) promoting the adhesion and differentiation of osteoblast-like cells while reducing bacterial adhesion to create a bioactive surface with potential for orthopaedic applications.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
</country>
<region>
<li>Île-de-France</li>
</region>
<settlement>
<li>Paris</li>
<li>Villetaneuse</li>
</settlement>
<orgName>
<li>Université Paris 13</li>
</orgName>
</list>
<tree>
<country name="France">
<region name="Île-de-France">
<name sortKey="Felgueiras, Helena P" sort="Felgueiras, Helena P" uniqKey="Felgueiras H" first="Helena P" last="Felgueiras">Helena P. Felgueiras</name>
</region>
<name sortKey="Aissa, Ines Ben" sort="Aissa, Ines Ben" uniqKey="Aissa I" first="Ines Ben" last="Aissa">Ines Ben Aissa</name>
<name sortKey="Migonney, Veronique" sort="Migonney, Veronique" uniqKey="Migonney V" first="Véronique" last="Migonney">Véronique Migonney</name>
</country>
<country name="Australie">
<noRegion>
<name sortKey="Evans, Margaret D M" sort="Evans, Margaret D M" uniqKey="Evans M" first="Margaret D M" last="Evans">Margaret D M. Evans</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002F91 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002F91 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Asie
   |area=    AustralieFrV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:26449451
   |texte=   Contributions of adhesive proteins to the cellular and bacterial response to surfaces treated with bioactive polymers: case of poly(sodium styrene sulfonate) grafted titanium surfaces.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:26449451" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a AustralieFrV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Dec 5 10:43:12 2017. Site generation: Tue Mar 5 14:07:20 2024