Effects of topographical surface modifications of electron beam melted Ti-6Al-4V titanium on human fetal osteoblasts
The aim of the study was to assess the suitability of different Ti‐6Al‐4V surfaces produced by the electron beam melting (EBM) process as matrices for attachment, proliferation, and differentiation of human fetal osteoblasts (hFOB 1.19). Human osteoblasts were cultured in vitro on smooth and rough‐t...
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creator | Ponader, Sabine Vairaktaris, Eleftherios Heinl, Peter Wilmowsky, Cornelius v. Rottmair, Andreas Körner, Carolin Singer, Robert F. Holst, Stefan Schlegel, Karl A. Neukam, Friedrich W. Nkenke, Emeka |
description | The aim of the study was to assess the suitability of different Ti‐6Al‐4V surfaces produced by the electron beam melting (EBM) process as matrices for attachment, proliferation, and differentiation of human fetal osteoblasts (hFOB 1.19). Human osteoblasts were cultured in vitro on smooth and rough‐textured Ti‐6Al‐4V alloy disks. By means of cell number and vitality and SEM micrographs cell attachment and proliferation were observed. The differentiation rate was examined by using quantitative real‐time PCR analysis for the gene expression of alkaline phosphatase (ALP), type I collagen (Coll‐I), bone sialoprotein (BSP) and osteocalcin (OC). After 3 days of incubation there was a significant higher vitality (p < 0.02) and proliferation (p < 0.02) of hFOB cells on smooth surfaces (Ra = 0.077 μm) and compact surfaces with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm). On these samples cells spread over almost the whole surface. On porous surfaces with higher Ra values, cell proliferation was reduced significantly. Quantitative real‐time PCR analysis showed that the expression of osteogenic differentiation markers was not influenced by surface characteristics. Gene expression did not differ more than twofold for the different samples. Compact titanium samples with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm) fabricated by the EBM process turned out to be best suited for cell proliferation, while highly rough surfaces (Ra ≥ 56.9 μm) reduced proliferation of hFOB cells. Surface characteristics of titanium can easily be changed by EBM in order to further improve proliferation. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008 |
doi_str_mv | 10.1002/jbm.a.31540 |
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Human osteoblasts were cultured in vitro on smooth and rough‐textured Ti‐6Al‐4V alloy disks. By means of cell number and vitality and SEM micrographs cell attachment and proliferation were observed. The differentiation rate was examined by using quantitative real‐time PCR analysis for the gene expression of alkaline phosphatase (ALP), type I collagen (Coll‐I), bone sialoprotein (BSP) and osteocalcin (OC). After 3 days of incubation there was a significant higher vitality (p < 0.02) and proliferation (p < 0.02) of hFOB cells on smooth surfaces (Ra = 0.077 μm) and compact surfaces with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm). On these samples cells spread over almost the whole surface. On porous surfaces with higher Ra values, cell proliferation was reduced significantly. Quantitative real‐time PCR analysis showed that the expression of osteogenic differentiation markers was not influenced by surface characteristics. Gene expression did not differ more than twofold for the different samples. Compact titanium samples with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm) fabricated by the EBM process turned out to be best suited for cell proliferation, while highly rough surfaces (Ra ≥ 56.9 μm) reduced proliferation of hFOB cells. Surface characteristics of titanium can easily be changed by EBM in order to further improve proliferation. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.31540</identifier><identifier>PMID: 17685409</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Anisotropy ; attachment ; Biocompatible Materials - metabolism ; Bone and Bones - embryology ; Cell Differentiation ; Cell Proliferation ; Cell Survival ; Cells, Cultured ; differentiation ; electron beam melting ; Electrons ; Gene Expression Regulation ; human osteoblasts ; Humans ; Osteoblasts - cytology ; Osteoblasts - metabolism ; proliferation ; Surface Properties ; surface roughness ; Temperature ; titanium ; Titanium - chemistry ; Titanium - pharmacology</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>The aim of the study was to assess the suitability of different Ti‐6Al‐4V surfaces produced by the electron beam melting (EBM) process as matrices for attachment, proliferation, and differentiation of human fetal osteoblasts (hFOB 1.19). Human osteoblasts were cultured in vitro on smooth and rough‐textured Ti‐6Al‐4V alloy disks. By means of cell number and vitality and SEM micrographs cell attachment and proliferation were observed. The differentiation rate was examined by using quantitative real‐time PCR analysis for the gene expression of alkaline phosphatase (ALP), type I collagen (Coll‐I), bone sialoprotein (BSP) and osteocalcin (OC). After 3 days of incubation there was a significant higher vitality (p < 0.02) and proliferation (p < 0.02) of hFOB cells on smooth surfaces (Ra = 0.077 μm) and compact surfaces with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm). On these samples cells spread over almost the whole surface. On porous surfaces with higher Ra values, cell proliferation was reduced significantly. Quantitative real‐time PCR analysis showed that the expression of osteogenic differentiation markers was not influenced by surface characteristics. Gene expression did not differ more than twofold for the different samples. Compact titanium samples with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm) fabricated by the EBM process turned out to be best suited for cell proliferation, while highly rough surfaces (Ra ≥ 56.9 μm) reduced proliferation of hFOB cells. Surface characteristics of titanium can easily be changed by EBM in order to further improve proliferation. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008</description><subject>Anisotropy</subject><subject>attachment</subject><subject>Biocompatible Materials - metabolism</subject><subject>Bone and Bones - embryology</subject><subject>Cell Differentiation</subject><subject>Cell Proliferation</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>differentiation</subject><subject>electron beam melting</subject><subject>Electrons</subject><subject>Gene Expression Regulation</subject><subject>human osteoblasts</subject><subject>Humans</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>proliferation</subject><subject>Surface Properties</subject><subject>surface roughness</subject><subject>Temperature</subject><subject>titanium</subject><subject>Titanium - chemistry</subject><subject>Titanium - pharmacology</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0ctvFSEUBnBiNPahK_eGlRszVxgeMyzrtbaa-kisj7ghZxiwVBiuA5Pa_17ae9Wdrjghv_MtzofQI0pWlJD22eUQV7BiVHByB-1TIdqGKynu3sxcNaxVcg8d5HxZsSSivY_2aCf7ytU-KsfOWVMyTg6XtEnfZthceAMB52V2YCyOafSu_hSfpltmQ12Y04QHCxFHG4od8blv5FFo-CdcfIHJLxFXcbFEmLCzpealXGwaAuSSH6B7DkK2D3fvIfr48vh8fdqcvTt5tT46awyXnDQg-OjsQAajBsk4QGcGTjpQBPpROtL3qlWGD5W1RDADvWh5J0apFFcgDTtET7a5mzn9WGwuOvpsbAgw2bRk3ZG2p4zQ_0JGO0FaTip8uoVmTjnP1unN7CPM15oSfdOGrm1o0LdtVP14F7sM0Y5_7e78FdAtuPLBXv8rS79-_uZ3aLPd8fWgP__swPxdy451Qn9-e6K7L-9PX3xYf9WU_QKrOaT-</recordid><startdate>20080315</startdate><enddate>20080315</enddate><creator>Ponader, Sabine</creator><creator>Vairaktaris, Eleftherios</creator><creator>Heinl, Peter</creator><creator>Wilmowsky, Cornelius v.</creator><creator>Rottmair, Andreas</creator><creator>Körner, Carolin</creator><creator>Singer, Robert F.</creator><creator>Holst, Stefan</creator><creator>Schlegel, Karl A.</creator><creator>Neukam, Friedrich W.</creator><creator>Nkenke, Emeka</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>20080315</creationdate><title>Effects of topographical surface modifications of electron beam melted Ti-6Al-4V titanium on human fetal osteoblasts</title><author>Ponader, Sabine ; Vairaktaris, Eleftherios ; Heinl, Peter ; Wilmowsky, Cornelius v. ; Rottmair, Andreas ; Körner, Carolin ; Singer, Robert F. ; Holst, Stefan ; Schlegel, Karl A. ; Neukam, Friedrich W. ; Nkenke, Emeka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4640-a54dfeb0bc9b634aa7cb407a90a8d6f088929c4b54d2053ca852475d69949a6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anisotropy</topic><topic>attachment</topic><topic>Biocompatible Materials - metabolism</topic><topic>Bone and Bones - embryology</topic><topic>Cell Differentiation</topic><topic>Cell Proliferation</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>differentiation</topic><topic>electron beam melting</topic><topic>Electrons</topic><topic>Gene Expression Regulation</topic><topic>human osteoblasts</topic><topic>Humans</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>proliferation</topic><topic>Surface Properties</topic><topic>surface roughness</topic><topic>Temperature</topic><topic>titanium</topic><topic>Titanium - chemistry</topic><topic>Titanium - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ponader, Sabine</creatorcontrib><creatorcontrib>Vairaktaris, Eleftherios</creatorcontrib><creatorcontrib>Heinl, Peter</creatorcontrib><creatorcontrib>Wilmowsky, Cornelius v.</creatorcontrib><creatorcontrib>Rottmair, Andreas</creatorcontrib><creatorcontrib>Körner, Carolin</creatorcontrib><creatorcontrib>Singer, Robert F.</creatorcontrib><creatorcontrib>Holst, Stefan</creatorcontrib><creatorcontrib>Schlegel, Karl A.</creatorcontrib><creatorcontrib>Neukam, Friedrich W.</creatorcontrib><creatorcontrib>Nkenke, Emeka</creatorcontrib><collection>Istex</collection><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>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ponader, Sabine</au><au>Vairaktaris, Eleftherios</au><au>Heinl, Peter</au><au>Wilmowsky, Cornelius v.</au><au>Rottmair, Andreas</au><au>Körner, Carolin</au><au>Singer, Robert F.</au><au>Holst, Stefan</au><au>Schlegel, Karl A.</au><au>Neukam, Friedrich W.</au><au>Nkenke, Emeka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of topographical surface modifications of electron beam melted Ti-6Al-4V titanium on human fetal osteoblasts</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2008-03-15</date><risdate>2008</risdate><volume>84A</volume><issue>4</issue><spage>1111</spage><epage>1119</epage><pages>1111-1119</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>The aim of the study was to assess the suitability of different Ti‐6Al‐4V surfaces produced by the electron beam melting (EBM) process as matrices for attachment, proliferation, and differentiation of human fetal osteoblasts (hFOB 1.19). Human osteoblasts were cultured in vitro on smooth and rough‐textured Ti‐6Al‐4V alloy disks. By means of cell number and vitality and SEM micrographs cell attachment and proliferation were observed. The differentiation rate was examined by using quantitative real‐time PCR analysis for the gene expression of alkaline phosphatase (ALP), type I collagen (Coll‐I), bone sialoprotein (BSP) and osteocalcin (OC). After 3 days of incubation there was a significant higher vitality (p < 0.02) and proliferation (p < 0.02) of hFOB cells on smooth surfaces (Ra = 0.077 μm) and compact surfaces with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm). On these samples cells spread over almost the whole surface. On porous surfaces with higher Ra values, cell proliferation was reduced significantly. Quantitative real‐time PCR analysis showed that the expression of osteogenic differentiation markers was not influenced by surface characteristics. Gene expression did not differ more than twofold for the different samples. Compact titanium samples with adherent partly molten titanium particles on the surface (Ra ≤ 24.9 μm) fabricated by the EBM process turned out to be best suited for cell proliferation, while highly rough surfaces (Ra ≥ 56.9 μm) reduced proliferation of hFOB cells. Surface characteristics of titanium can easily be changed by EBM in order to further improve proliferation. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17685409</pmid><doi>10.1002/jbm.a.31540</doi><tpages>9</tpages></addata></record> |
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subjects | Anisotropy attachment Biocompatible Materials - metabolism Bone and Bones - embryology Cell Differentiation Cell Proliferation Cell Survival Cells, Cultured differentiation electron beam melting Electrons Gene Expression Regulation human osteoblasts Humans Osteoblasts - cytology Osteoblasts - metabolism proliferation Surface Properties surface roughness Temperature titanium Titanium - chemistry Titanium - pharmacology |
title | Effects of topographical surface modifications of electron beam melted Ti-6Al-4V titanium on human fetal osteoblasts |
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