Biocompatibility markers for the study of interactions between osteoblasts and composite biomaterials
Abstract Biphasic calcium phosphate (BCP), a mixture of hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP), has attracted attention as an excellent bone graft substitute. Mixtures of ceramics with agarose, as natural biodegradable binder, have been recently performed in order to increase the fle...
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Veröffentlicht in: | Biomaterials 2009-01, Vol.30 (1), p.45-51 |
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description | Abstract Biphasic calcium phosphate (BCP), a mixture of hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP), has attracted attention as an excellent bone graft substitute. Mixtures of ceramics with agarose, as natural biodegradable binder, have been recently performed in order to increase the flexibility of the ceramic component and to facilitate the biomaterial preparation. In previous studies we have evaluated the response of both L929 fibroblasts and Saos-2 osteoblasts to hydroxyapatite–βTCP/agarose disks observing a higher sensitivity of osteoblasts to this biomaterial. In the present study, the use of specific fluorescent probes and antibodies has allowed to evaluate different cell function parameters as biocompatibility markers for the cell/biomaterial interaction of Saos-2 osteoblasts cultured for 7 days on hydroxyapatite–βTCP/agarose disks. The cell cycle sub G1 fraction, the exposition of phosphatidylserine on the outside surface of the plasma membrane and the analysis of plasma membrane integrity versus cell size, indicate that the interaction with the biomaterial induces a light increase of apoptosis in osteoblasts without producing cell necrosis. The high percentage of viable cells on the biomaterial and the preservation of endothelial nitric oxide synthase (eNOS) expression, eNOS activity and mitochondrial membrane potential (Δψm ), demonstrate the good biocompatibility of hydroxyapatite–βTCP/agarose disks and its potential utility for bone substitution and repair. |
doi_str_mv | 10.1016/j.biomaterials.2008.09.012 |
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Mixtures of ceramics with agarose, as natural biodegradable binder, have been recently performed in order to increase the flexibility of the ceramic component and to facilitate the biomaterial preparation. In previous studies we have evaluated the response of both L929 fibroblasts and Saos-2 osteoblasts to hydroxyapatite–βTCP/agarose disks observing a higher sensitivity of osteoblasts to this biomaterial. In the present study, the use of specific fluorescent probes and antibodies has allowed to evaluate different cell function parameters as biocompatibility markers for the cell/biomaterial interaction of Saos-2 osteoblasts cultured for 7 days on hydroxyapatite–βTCP/agarose disks. The cell cycle sub G1 fraction, the exposition of phosphatidylserine on the outside surface of the plasma membrane and the analysis of plasma membrane integrity versus cell size, indicate that the interaction with the biomaterial induces a light increase of apoptosis in osteoblasts without producing cell necrosis. The high percentage of viable cells on the biomaterial and the preservation of endothelial nitric oxide synthase (eNOS) expression, eNOS activity and mitochondrial membrane potential (Δψm ), demonstrate the good biocompatibility of hydroxyapatite–βTCP/agarose disks and its potential utility for bone substitution and repair.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2008.09.012</identifier><identifier>PMID: 18838165</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Agarose ; Annexin A5 - metabolism ; Apoptosis - drug effects ; Biocompatible Materials - pharmacology ; Biomarkers - metabolism ; Biphasic calcium phosphate ; Bone graft ; Cell Cycle - drug effects ; Cell Line, Tumor ; Dentistry ; Humans ; Membrane Potential, Mitochondrial - drug effects ; Necrosis ; Nitric oxide ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type III - metabolism ; Osteoblasts - drug effects ; Osteoblasts - enzymology ; Osteoblasts - metabolism ; Osteoblasts - pathology ; Phosphatidylserines - metabolism ; Saos-2 osteoblasts</subject><ispartof>Biomaterials, 2009-01, Vol.30 (1), p.45-51</ispartof><rights>Elsevier Ltd</rights><rights>2008 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-d9f6dbe1f441edaad409e204f3e0c46caf3662b58cc3becd7e8f6ab7359512ca3</citedby><cites>FETCH-LOGICAL-c562t-d9f6dbe1f441edaad409e204f3e0c46caf3662b58cc3becd7e8f6ab7359512ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biomaterials.2008.09.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3538,27906,27907,45977</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18838165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alcaide, María</creatorcontrib><creatorcontrib>Serrano, María-Concepción</creatorcontrib><creatorcontrib>Pagani, Raffaella</creatorcontrib><creatorcontrib>Sánchez-Salcedo, Sandra</creatorcontrib><creatorcontrib>Vallet-Regí, María</creatorcontrib><creatorcontrib>Portolés, María-Teresa</creatorcontrib><title>Biocompatibility markers for the study of interactions between osteoblasts and composite biomaterials</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract Biphasic calcium phosphate (BCP), a mixture of hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP), has attracted attention as an excellent bone graft substitute. Mixtures of ceramics with agarose, as natural biodegradable binder, have been recently performed in order to increase the flexibility of the ceramic component and to facilitate the biomaterial preparation. In previous studies we have evaluated the response of both L929 fibroblasts and Saos-2 osteoblasts to hydroxyapatite–βTCP/agarose disks observing a higher sensitivity of osteoblasts to this biomaterial. In the present study, the use of specific fluorescent probes and antibodies has allowed to evaluate different cell function parameters as biocompatibility markers for the cell/biomaterial interaction of Saos-2 osteoblasts cultured for 7 days on hydroxyapatite–βTCP/agarose disks. The cell cycle sub G1 fraction, the exposition of phosphatidylserine on the outside surface of the plasma membrane and the analysis of plasma membrane integrity versus cell size, indicate that the interaction with the biomaterial induces a light increase of apoptosis in osteoblasts without producing cell necrosis. The high percentage of viable cells on the biomaterial and the preservation of endothelial nitric oxide synthase (eNOS) expression, eNOS activity and mitochondrial membrane potential (Δψm ), demonstrate the good biocompatibility of hydroxyapatite–βTCP/agarose disks and its potential utility for bone substitution and repair.</description><subject>Advanced Basic Science</subject><subject>Agarose</subject><subject>Annexin A5 - metabolism</subject><subject>Apoptosis - drug effects</subject><subject>Biocompatible Materials - pharmacology</subject><subject>Biomarkers - metabolism</subject><subject>Biphasic calcium phosphate</subject><subject>Bone graft</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Line, Tumor</subject><subject>Dentistry</subject><subject>Humans</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Necrosis</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Osteoblasts - drug effects</subject><subject>Osteoblasts - enzymology</subject><subject>Osteoblasts - metabolism</subject><subject>Osteoblasts - pathology</subject><subject>Phosphatidylserines - metabolism</subject><subject>Saos-2 osteoblasts</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk-LFDEQxRtR3NnVryDBg566rSSddNqDsO76DxY8qOAtpJNqzGxPZ0zSynx708yAiwfZUxH4vfdCvaqq5xQaClS-2jaDDzuTMXozpYYBqAb6Bih7UG2o6lQtehAPqw3QltW9pOysOk9pC-UNLXtcnVGluKJSbCp864MNu73JfvCTzweyM_EWYyJjiCT_QJLy4g4kjMTPJdHY7MOcyID5N-JMQsoYhsmknIiZHVm9QvIZyd0_PqkejWXg09O8qL69f_f16mN98_nDp6vLm9oKyXLt-lG6AenYthSdMa6FHhm0I0ewrbRm5FKyQShr-YDWdahGaYaOi15QZg2_qF4effcx_FwwZb3zyeI0mRnDknTHW0q5Yl0hX_yX5KKTAjjcA5QglKQFfH0EbQwpRRz1PvqyzIOmoNfe9Fbf3Ylee9PQ69JbET87pSzDDt1f6amoAlwfASzr--Ux6mQ9zhadj2izdsHfL-fNPzZ28rO3ZrrFA6ZtWOK8aqhOTIP-sl7QekCgAGQP3_kfQ07Ilg</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Alcaide, María</creator><creator>Serrano, María-Concepción</creator><creator>Pagani, Raffaella</creator><creator>Sánchez-Salcedo, Sandra</creator><creator>Vallet-Regí, María</creator><creator>Portolés, María-Teresa</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Biocompatibility markers for the study of interactions between osteoblasts and composite biomaterials</title><author>Alcaide, María ; Serrano, María-Concepción ; Pagani, Raffaella ; Sánchez-Salcedo, Sandra ; Vallet-Regí, María ; Portolés, María-Teresa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-d9f6dbe1f441edaad409e204f3e0c46caf3662b58cc3becd7e8f6ab7359512ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Advanced Basic Science</topic><topic>Agarose</topic><topic>Annexin A5 - metabolism</topic><topic>Apoptosis - drug effects</topic><topic>Biocompatible Materials - pharmacology</topic><topic>Biomarkers - metabolism</topic><topic>Biphasic calcium phosphate</topic><topic>Bone graft</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Line, Tumor</topic><topic>Dentistry</topic><topic>Humans</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Necrosis</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Osteoblasts - drug effects</topic><topic>Osteoblasts - enzymology</topic><topic>Osteoblasts - metabolism</topic><topic>Osteoblasts - pathology</topic><topic>Phosphatidylserines - metabolism</topic><topic>Saos-2 osteoblasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alcaide, María</creatorcontrib><creatorcontrib>Serrano, María-Concepción</creatorcontrib><creatorcontrib>Pagani, Raffaella</creatorcontrib><creatorcontrib>Sánchez-Salcedo, Sandra</creatorcontrib><creatorcontrib>Vallet-Regí, María</creatorcontrib><creatorcontrib>Portolés, María-Teresa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alcaide, María</au><au>Serrano, María-Concepción</au><au>Pagani, Raffaella</au><au>Sánchez-Salcedo, Sandra</au><au>Vallet-Regí, María</au><au>Portolés, María-Teresa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biocompatibility markers for the study of interactions between osteoblasts and composite biomaterials</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>30</volume><issue>1</issue><spage>45</spage><epage>51</epage><pages>45-51</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract Biphasic calcium phosphate (BCP), a mixture of hydroxyapatite (HA) and β-tricalcium phosphate (β-TCP), has attracted attention as an excellent bone graft substitute. Mixtures of ceramics with agarose, as natural biodegradable binder, have been recently performed in order to increase the flexibility of the ceramic component and to facilitate the biomaterial preparation. In previous studies we have evaluated the response of both L929 fibroblasts and Saos-2 osteoblasts to hydroxyapatite–βTCP/agarose disks observing a higher sensitivity of osteoblasts to this biomaterial. In the present study, the use of specific fluorescent probes and antibodies has allowed to evaluate different cell function parameters as biocompatibility markers for the cell/biomaterial interaction of Saos-2 osteoblasts cultured for 7 days on hydroxyapatite–βTCP/agarose disks. The cell cycle sub G1 fraction, the exposition of phosphatidylserine on the outside surface of the plasma membrane and the analysis of plasma membrane integrity versus cell size, indicate that the interaction with the biomaterial induces a light increase of apoptosis in osteoblasts without producing cell necrosis. The high percentage of viable cells on the biomaterial and the preservation of endothelial nitric oxide synthase (eNOS) expression, eNOS activity and mitochondrial membrane potential (Δψm ), demonstrate the good biocompatibility of hydroxyapatite–βTCP/agarose disks and its potential utility for bone substitution and repair.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>18838165</pmid><doi>10.1016/j.biomaterials.2008.09.012</doi><tpages>7</tpages></addata></record> |
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subjects | Advanced Basic Science Agarose Annexin A5 - metabolism Apoptosis - drug effects Biocompatible Materials - pharmacology Biomarkers - metabolism Biphasic calcium phosphate Bone graft Cell Cycle - drug effects Cell Line, Tumor Dentistry Humans Membrane Potential, Mitochondrial - drug effects Necrosis Nitric oxide Nitric Oxide - metabolism Nitric Oxide Synthase Type III - metabolism Osteoblasts - drug effects Osteoblasts - enzymology Osteoblasts - metabolism Osteoblasts - pathology Phosphatidylserines - metabolism Saos-2 osteoblasts |
title | Biocompatibility markers for the study of interactions between osteoblasts and composite biomaterials |
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