Rapid quantitative bioassay of osteoinduction
We developed a reproducible, relatively rapid bioassay that quantitatively correlates with the osteoinductive capacity of demineralized bone matrix obtained from human long bones. We have found that Saos human osteosarcoma cells proliferate in response to incubation with demineralized bone matrix an...
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creator | Adkisson, Huston Davis Strauss-Schoenberger, Jena Gillis, Mary Wilkins, Ross Jackson, Marc Hruska, Keith A. |
description | We developed a reproducible, relatively rapid bioassay that quantitatively correlates with the osteoinductive capacity of demineralized bone matrix obtained from human long bones. We have found that Saos human osteosarcoma cells proliferate in response to incubation with demineralized bone matrix and that an index of this proliferative activity correlates with demineralized bone matrix‐induced osteogenesis in vivo. The bioassay (Saos cell proliferation) had an interassay coefficient of variation of 23 ± 2% and an intra‐assay cocfficient of 11 ± 1%. Cell proliferation was normalized to a standard sample of demineralized bone matrix with a clinically high osteoinductive capacity, which was assigned a value of one. The Saos cell proliferation for each sample was related to the standard and assigned a value placing it into thc low (0.00‐0.39), intermediate (0.40‐0.69). or high (0.70‐1.49) osteoinductivc index group. Osteoinduction of human demineralized bone matrix was quantitated by expressing new bone formation as a function of the total bone volume (new bone plus the demineralized bone powder). The demineralized bone matrix was placed in pouches formed in the rectus abdominis muscles of athymic rats, and endochondral bone formation was assessed at 35 days following implantation, when marrow spaces in the ossicles were formed by new bone bridging the spaces between demineralized bone matrix particles. The proliferative index correlated with the area of new bone formation in histological sections ol the newly formed ossicles. When the proliferative index (the osteoinductive index) was divided into low, intermediate. and high groups, the correlation between it and new bone formation (osteoinduction) was 0.850 (p < 0.0005) in 25 samples of demineralized bone matrix. There was no overlap in the osteoinduction stimulated between the samples with low and high osteoinductive indices. We conclude that the proliferation assay is useful for the routine screening of bone allograft donors for osteoinductivc potential. Furthermore, the two‐dimensional area of new bone formation. as it relates to total new bone area, is a quantitative measure of osteoinduction. |
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We have found that Saos human osteosarcoma cells proliferate in response to incubation with demineralized bone matrix and that an index of this proliferative activity correlates with demineralized bone matrix‐induced osteogenesis in vivo. The bioassay (Saos cell proliferation) had an interassay coefficient of variation of 23 ± 2% and an intra‐assay cocfficient of 11 ± 1%. Cell proliferation was normalized to a standard sample of demineralized bone matrix with a clinically high osteoinductive capacity, which was assigned a value of one. The Saos cell proliferation for each sample was related to the standard and assigned a value placing it into thc low (0.00‐0.39), intermediate (0.40‐0.69). or high (0.70‐1.49) osteoinductivc index group. Osteoinduction of human demineralized bone matrix was quantitated by expressing new bone formation as a function of the total bone volume (new bone plus the demineralized bone powder). The demineralized bone matrix was placed in pouches formed in the rectus abdominis muscles of athymic rats, and endochondral bone formation was assessed at 35 days following implantation, when marrow spaces in the ossicles were formed by new bone bridging the spaces between demineralized bone matrix particles. The proliferative index correlated with the area of new bone formation in histological sections ol the newly formed ossicles. When the proliferative index (the osteoinductive index) was divided into low, intermediate. and high groups, the correlation between it and new bone formation (osteoinduction) was 0.850 (p < 0.0005) in 25 samples of demineralized bone matrix. There was no overlap in the osteoinduction stimulated between the samples with low and high osteoinductive indices. We conclude that the proliferation assay is useful for the routine screening of bone allograft donors for osteoinductivc potential. Furthermore, the two‐dimensional area of new bone formation. as it relates to total new bone area, is a quantitative measure of osteoinduction.</description><identifier>ISSN: 0736-0266</identifier><identifier>EISSN: 1554-527X</identifier><identifier>DOI: 10.1002/jor.1100180326</identifier><identifier>PMID: 10937641</identifier><identifier>CODEN: JOREDR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Aged ; Alkaline Phosphatase - metabolism ; Bioassay ; Biological Assay ; Bone ; Bone Development ; Bone Matrix - physiology ; Calcification, Physiologic ; Cell Division ; Cytology ; Female ; Humans ; Male ; Middle Aged ; Oncology ; Osteosarcoma - pathology ; Space life sciences ; Thymidine - metabolism ; Tumor Cells, Cultured</subject><ispartof>Journal of orthopaedic research, 2000-05, Vol.18 (3), p.503-511</ispartof><rights>Copyright © 2000 Orthopaedic Research Society</rights><rights>Copyright Journal of Bone and Joint Surgery, Inc. May 2000</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4376-e41bd746575269cf117614e2bea54a40d6091ba3e627293111347ea1bfd43fcd3</citedby><cites>FETCH-LOGICAL-c4376-e41bd746575269cf117614e2bea54a40d6091ba3e627293111347ea1bfd43fcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjor.1100180326$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjor.1100180326$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10937641$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adkisson, Huston Davis</creatorcontrib><creatorcontrib>Strauss-Schoenberger, Jena</creatorcontrib><creatorcontrib>Gillis, Mary</creatorcontrib><creatorcontrib>Wilkins, Ross</creatorcontrib><creatorcontrib>Jackson, Marc</creatorcontrib><creatorcontrib>Hruska, Keith A.</creatorcontrib><title>Rapid quantitative bioassay of osteoinduction</title><title>Journal of orthopaedic research</title><addtitle>J. Orthop. Res</addtitle><description>We developed a reproducible, relatively rapid bioassay that quantitatively correlates with the osteoinductive capacity of demineralized bone matrix obtained from human long bones. We have found that Saos human osteosarcoma cells proliferate in response to incubation with demineralized bone matrix and that an index of this proliferative activity correlates with demineralized bone matrix‐induced osteogenesis in vivo. The bioassay (Saos cell proliferation) had an interassay coefficient of variation of 23 ± 2% and an intra‐assay cocfficient of 11 ± 1%. Cell proliferation was normalized to a standard sample of demineralized bone matrix with a clinically high osteoinductive capacity, which was assigned a value of one. The Saos cell proliferation for each sample was related to the standard and assigned a value placing it into thc low (0.00‐0.39), intermediate (0.40‐0.69). or high (0.70‐1.49) osteoinductivc index group. Osteoinduction of human demineralized bone matrix was quantitated by expressing new bone formation as a function of the total bone volume (new bone plus the demineralized bone powder). The demineralized bone matrix was placed in pouches formed in the rectus abdominis muscles of athymic rats, and endochondral bone formation was assessed at 35 days following implantation, when marrow spaces in the ossicles were formed by new bone bridging the spaces between demineralized bone matrix particles. The proliferative index correlated with the area of new bone formation in histological sections ol the newly formed ossicles. When the proliferative index (the osteoinductive index) was divided into low, intermediate. and high groups, the correlation between it and new bone formation (osteoinduction) was 0.850 (p < 0.0005) in 25 samples of demineralized bone matrix. There was no overlap in the osteoinduction stimulated between the samples with low and high osteoinductive indices. We conclude that the proliferation assay is useful for the routine screening of bone allograft donors for osteoinductivc potential. Furthermore, the two‐dimensional area of new bone formation. as it relates to total new bone area, is a quantitative measure of osteoinduction.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Bioassay</subject><subject>Biological Assay</subject><subject>Bone</subject><subject>Bone Development</subject><subject>Bone Matrix - physiology</subject><subject>Calcification, Physiologic</subject><subject>Cell Division</subject><subject>Cytology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Osteosarcoma - pathology</subject><subject>Space life sciences</subject><subject>Thymidine - metabolism</subject><subject>Tumor Cells, Cultured</subject><issn>0736-0266</issn><issn>1554-527X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkTtPwzAURi0EglJYGVHFwJbi6ycZUQUFVFGpPDfLSRzJpY1bOwH67zFKxWvpdO9wviPd7yJ0BLgPGJOzqfN9iBucY0rEFuoA5yzhRL5sow6WVCSYCLGH9kOYYowlkPNdtAc4pVIw6KBkohe26C0bXdW21rV9M73MOh2CXvVc2XOhNs5WRZPX1lUHaKfUs2AO17OLHq8uHwbXyWg8vBlcjJKcRW9iGGSFZIJLTkSalwBSADMkM5ozzXAhcAqZpkYQSVIKAJRJoyErC0bLvKBddNp6F94tGxNqNbchN7OZroxrgpIgOWUcNoIEGEshFRE8-QdOXeOreIQilAPmmOAI9Vso9y4Eb0q18Hau_UoBVl91x5BXP3XHwPHa2mRzU_zC234jkLbAu52Z1Qaduh1P_siTNmvjDz6-s9q_KiGp5Or5bqie2P0dHaUT9UI_Ab-YmLI</recordid><startdate>200005</startdate><enddate>200005</enddate><creator>Adkisson, Huston Davis</creator><creator>Strauss-Schoenberger, Jena</creator><creator>Gillis, Mary</creator><creator>Wilkins, Ross</creator><creator>Jackson, Marc</creator><creator>Hruska, Keith A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Blackwell Publishing Ltd</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200005</creationdate><title>Rapid quantitative bioassay of osteoinduction</title><author>Adkisson, Huston Davis ; Strauss-Schoenberger, Jena ; Gillis, Mary ; Wilkins, Ross ; Jackson, Marc ; Hruska, Keith A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4376-e41bd746575269cf117614e2bea54a40d6091ba3e627293111347ea1bfd43fcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Bioassay</topic><topic>Biological Assay</topic><topic>Bone</topic><topic>Bone Development</topic><topic>Bone Matrix - physiology</topic><topic>Calcification, Physiologic</topic><topic>Cell Division</topic><topic>Cytology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Osteosarcoma - pathology</topic><topic>Space life sciences</topic><topic>Thymidine - metabolism</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adkisson, Huston Davis</creatorcontrib><creatorcontrib>Strauss-Schoenberger, Jena</creatorcontrib><creatorcontrib>Gillis, Mary</creatorcontrib><creatorcontrib>Wilkins, Ross</creatorcontrib><creatorcontrib>Jackson, Marc</creatorcontrib><creatorcontrib>Hruska, Keith A.</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of orthopaedic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adkisson, Huston Davis</au><au>Strauss-Schoenberger, Jena</au><au>Gillis, Mary</au><au>Wilkins, Ross</au><au>Jackson, Marc</au><au>Hruska, Keith A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid quantitative bioassay of osteoinduction</atitle><jtitle>Journal of orthopaedic research</jtitle><addtitle>J. Orthop. Res</addtitle><date>2000-05</date><risdate>2000</risdate><volume>18</volume><issue>3</issue><spage>503</spage><epage>511</epage><pages>503-511</pages><issn>0736-0266</issn><eissn>1554-527X</eissn><coden>JOREDR</coden><abstract>We developed a reproducible, relatively rapid bioassay that quantitatively correlates with the osteoinductive capacity of demineralized bone matrix obtained from human long bones. We have found that Saos human osteosarcoma cells proliferate in response to incubation with demineralized bone matrix and that an index of this proliferative activity correlates with demineralized bone matrix‐induced osteogenesis in vivo. The bioassay (Saos cell proliferation) had an interassay coefficient of variation of 23 ± 2% and an intra‐assay cocfficient of 11 ± 1%. Cell proliferation was normalized to a standard sample of demineralized bone matrix with a clinically high osteoinductive capacity, which was assigned a value of one. The Saos cell proliferation for each sample was related to the standard and assigned a value placing it into thc low (0.00‐0.39), intermediate (0.40‐0.69). or high (0.70‐1.49) osteoinductivc index group. Osteoinduction of human demineralized bone matrix was quantitated by expressing new bone formation as a function of the total bone volume (new bone plus the demineralized bone powder). The demineralized bone matrix was placed in pouches formed in the rectus abdominis muscles of athymic rats, and endochondral bone formation was assessed at 35 days following implantation, when marrow spaces in the ossicles were formed by new bone bridging the spaces between demineralized bone matrix particles. The proliferative index correlated with the area of new bone formation in histological sections ol the newly formed ossicles. When the proliferative index (the osteoinductive index) was divided into low, intermediate. and high groups, the correlation between it and new bone formation (osteoinduction) was 0.850 (p < 0.0005) in 25 samples of demineralized bone matrix. There was no overlap in the osteoinduction stimulated between the samples with low and high osteoinductive indices. We conclude that the proliferation assay is useful for the routine screening of bone allograft donors for osteoinductivc potential. Furthermore, the two‐dimensional area of new bone formation. as it relates to total new bone area, is a quantitative measure of osteoinduction.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>10937641</pmid><doi>10.1002/jor.1100180326</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Aged Alkaline Phosphatase - metabolism Bioassay Biological Assay Bone Bone Development Bone Matrix - physiology Calcification, Physiologic Cell Division Cytology Female Humans Male Middle Aged Oncology Osteosarcoma - pathology Space life sciences Thymidine - metabolism Tumor Cells, Cultured |
title | Rapid quantitative bioassay of osteoinduction |
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