Repair of segmental bone defect using Totally Vitalized tissue engineered bone graft by a combined perfusion seeding and culture system

The basic strategy to construct tissue engineered bone graft (TEBG) is to combine osteoblastic cells with three dimensional (3D) scaffold. Based on this strategy, we proposed the "Totally Vitalized TEBG" (TV-TEBG) which was characterized by abundant and homogenously distributed cells with...

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Veröffentlicht in:PloS one 2014-04, Vol.9 (4), p.e94276
Hauptverfasser: Wang, Lin, Ma, Xiang-Yu, Zhang, Yang, Feng, Ya-Fei, Li, Xiang, Hu, Yun-Yu, Wang, Zhen, Ma, Zhen-Sheng, Lei, Wei
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Ma, Xiang-Yu
Zhang, Yang
Feng, Ya-Fei
Li, Xiang
Hu, Yun-Yu
Wang, Zhen
Ma, Zhen-Sheng
Lei, Wei
description The basic strategy to construct tissue engineered bone graft (TEBG) is to combine osteoblastic cells with three dimensional (3D) scaffold. Based on this strategy, we proposed the "Totally Vitalized TEBG" (TV-TEBG) which was characterized by abundant and homogenously distributed cells with enhanced cell proliferation and differentiation and further investigated its biological performance in repairing segmental bone defect. In this study, we constructed the TV-TEBG with the combination of customized flow perfusion seeding/culture system and β-tricalcium phosphate (β-TCP) scaffold fabricated by Rapid Prototyping (RP) technique. We systemically compared three kinds of TEBG constructed by perfusion seeding and perfusion culture (PSPC) method, static seeding and perfusion culture (SSPC) method, and static seeding and static culture (SSSC) method for their in vitro performance and bone defect healing efficacy with a rabbit model. Our study has demonstrated that TEBG constructed by PSPC method exhibited better biological properties with higher daily D-glucose consumption, increased cell proliferation and differentiation, and better cell distribution, indicating the successful construction of TV-TEBG. After implanted into rabbit radius defects for 12 weeks, PSPC group exerted higher X-ray score close to autograft, much greater mechanical property evidenced by the biomechanical testing and significantly higher new bone formation as shown by histological analysis compared with the other two groups, and eventually obtained favorable healing efficacy of the segmental bone defect that was the closest to autograft transplantation. This study demonstrated the feasibility of TV-TEBG construction with combination of perfusion seeding, perfusion culture and RP technique which exerted excellent biological properties. The application of TV-TEBG may become a preferred candidate for segmental bone defect repair in orthopedic and maxillofacial fields.
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Based on this strategy, we proposed the "Totally Vitalized TEBG" (TV-TEBG) which was characterized by abundant and homogenously distributed cells with enhanced cell proliferation and differentiation and further investigated its biological performance in repairing segmental bone defect. In this study, we constructed the TV-TEBG with the combination of customized flow perfusion seeding/culture system and β-tricalcium phosphate (β-TCP) scaffold fabricated by Rapid Prototyping (RP) technique. We systemically compared three kinds of TEBG constructed by perfusion seeding and perfusion culture (PSPC) method, static seeding and perfusion culture (SSPC) method, and static seeding and static culture (SSSC) method for their in vitro performance and bone defect healing efficacy with a rabbit model. Our study has demonstrated that TEBG constructed by PSPC method exhibited better biological properties with higher daily D-glucose consumption, increased cell proliferation and differentiation, and better cell distribution, indicating the successful construction of TV-TEBG. After implanted into rabbit radius defects for 12 weeks, PSPC group exerted higher X-ray score close to autograft, much greater mechanical property evidenced by the biomechanical testing and significantly higher new bone formation as shown by histological analysis compared with the other two groups, and eventually obtained favorable healing efficacy of the segmental bone defect that was the closest to autograft transplantation. This study demonstrated the feasibility of TV-TEBG construction with combination of perfusion seeding, perfusion culture and RP technique which exerted excellent biological properties. The application of TV-TEBG may become a preferred candidate for segmental bone defect repair in orthopedic and maxillofacial fields.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0094276</identifier><identifier>PMID: 24728277</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alkaline Phosphatase - metabolism ; Animals ; Biocompatibility ; Bioengineering ; Biological properties ; Biology and Life Sciences ; Biomechanical Phenomena - drug effects ; Biomechanics ; Biomedical materials ; Bioreactors ; Bone diseases ; Bone grafts ; Bone growth ; Bone healing ; Bone marrow ; Bone Regeneration - drug effects ; Bone Transplantation ; Bone-grafting ; Bones ; Calcium phosphates ; Calcium Phosphates - pharmacology ; Care and treatment ; Cell adhesion &amp; migration ; Cell culture ; Cell growth ; Cell proliferation ; Cell Survival - drug effects ; Compressive Strength - drug effects ; Construction ; Construction methods ; Defects ; Design ; Diagnosis ; Differentiation ; Engineering and Technology ; Feasibility studies ; Fluorescence ; Fluorescent Dyes - metabolism ; Glucose ; Glucose - metabolism ; Grafting ; Healing ; Hydroxyapatite ; Implants, Experimental ; In vitro methods and tests ; Maxillofacial ; Medicine and Health Sciences ; Methods ; Morphology ; Orthopedics ; Osteoblasts ; Osteoblasts - cytology ; Osteoblasts - drug effects ; Osteoblasts - enzymology ; Osteogenesis ; Perfusion ; Phosphates ; Physiological aspects ; Rabbits ; Radius ; Radius - diagnostic imaging ; Radius - drug effects ; Radius - pathology ; Radius - surgery ; Rapid prototyping ; Repair ; Shear stress ; Skin &amp; tissue grafts ; Staining and Labeling ; Stem cells ; Studies ; Time Factors ; Tissue Culture Techniques ; Tissue engineering ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry ; Transplantation ; Tricalcium phosphate ; Wound Healing - drug effects ; X-Ray Microtomography</subject><ispartof>PloS one, 2014-04, Vol.9 (4), p.e94276</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Wang et al 2014 Wang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-b3cb295ad7ebf395ae992e5c8aaa0cf8bc6ed39d01d2ea9161f0fd8b377ff4c3</citedby><cites>FETCH-LOGICAL-c692t-b3cb295ad7ebf395ae992e5c8aaa0cf8bc6ed39d01d2ea9161f0fd8b377ff4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984127/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984127/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24728277$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Awad, Hani A.</contributor><creatorcontrib>Wang, Lin</creatorcontrib><creatorcontrib>Ma, Xiang-Yu</creatorcontrib><creatorcontrib>Zhang, Yang</creatorcontrib><creatorcontrib>Feng, Ya-Fei</creatorcontrib><creatorcontrib>Li, Xiang</creatorcontrib><creatorcontrib>Hu, Yun-Yu</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Ma, Zhen-Sheng</creatorcontrib><creatorcontrib>Lei, Wei</creatorcontrib><title>Repair of segmental bone defect using Totally Vitalized tissue engineered bone graft by a combined perfusion seeding and culture system</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The basic strategy to construct tissue engineered bone graft (TEBG) is to combine osteoblastic cells with three dimensional (3D) scaffold. Based on this strategy, we proposed the "Totally Vitalized TEBG" (TV-TEBG) which was characterized by abundant and homogenously distributed cells with enhanced cell proliferation and differentiation and further investigated its biological performance in repairing segmental bone defect. In this study, we constructed the TV-TEBG with the combination of customized flow perfusion seeding/culture system and β-tricalcium phosphate (β-TCP) scaffold fabricated by Rapid Prototyping (RP) technique. We systemically compared three kinds of TEBG constructed by perfusion seeding and perfusion culture (PSPC) method, static seeding and perfusion culture (SSPC) method, and static seeding and static culture (SSSC) method for their in vitro performance and bone defect healing efficacy with a rabbit model. Our study has demonstrated that TEBG constructed by PSPC method exhibited better biological properties with higher daily D-glucose consumption, increased cell proliferation and differentiation, and better cell distribution, indicating the successful construction of TV-TEBG. After implanted into rabbit radius defects for 12 weeks, PSPC group exerted higher X-ray score close to autograft, much greater mechanical property evidenced by the biomechanical testing and significantly higher new bone formation as shown by histological analysis compared with the other two groups, and eventually obtained favorable healing efficacy of the segmental bone defect that was the closest to autograft transplantation. This study demonstrated the feasibility of TV-TEBG construction with combination of perfusion seeding, perfusion culture and RP technique which exerted excellent biological properties. The application of TV-TEBG may become a preferred candidate for segmental bone defect repair in orthopedic and maxillofacial fields.</description><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Bioengineering</subject><subject>Biological properties</subject><subject>Biology and Life Sciences</subject><subject>Biomechanical Phenomena - drug effects</subject><subject>Biomechanics</subject><subject>Biomedical materials</subject><subject>Bioreactors</subject><subject>Bone diseases</subject><subject>Bone grafts</subject><subject>Bone growth</subject><subject>Bone healing</subject><subject>Bone marrow</subject><subject>Bone Regeneration - drug effects</subject><subject>Bone Transplantation</subject><subject>Bone-grafting</subject><subject>Bones</subject><subject>Calcium phosphates</subject><subject>Calcium Phosphates - pharmacology</subject><subject>Care and treatment</subject><subject>Cell adhesion &amp; migration</subject><subject>Cell culture</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Cell Survival - drug effects</subject><subject>Compressive Strength - drug effects</subject><subject>Construction</subject><subject>Construction methods</subject><subject>Defects</subject><subject>Design</subject><subject>Diagnosis</subject><subject>Differentiation</subject><subject>Engineering and Technology</subject><subject>Feasibility studies</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Grafting</subject><subject>Healing</subject><subject>Hydroxyapatite</subject><subject>Implants, Experimental</subject><subject>In vitro methods and tests</subject><subject>Maxillofacial</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Morphology</subject><subject>Orthopedics</subject><subject>Osteoblasts</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - drug effects</subject><subject>Osteoblasts - enzymology</subject><subject>Osteogenesis</subject><subject>Perfusion</subject><subject>Phosphates</subject><subject>Physiological aspects</subject><subject>Rabbits</subject><subject>Radius</subject><subject>Radius - diagnostic imaging</subject><subject>Radius - drug effects</subject><subject>Radius - pathology</subject><subject>Radius - surgery</subject><subject>Rapid prototyping</subject><subject>Repair</subject><subject>Shear stress</subject><subject>Skin &amp; tissue grafts</subject><subject>Staining and Labeling</subject><subject>Stem cells</subject><subject>Studies</subject><subject>Time Factors</subject><subject>Tissue Culture Techniques</subject><subject>Tissue engineering</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Transplantation</subject><subject>Tricalcium phosphate</subject><subject>Wound Healing - drug effects</subject><subject>X-Ray Microtomography</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</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><sourceid>DOA</sourceid><recordid>eNqNk11rFDEUhgdRbK3-A9GAIHqxaz5mJpObQil-FAqFWnobMsnJNGVmsiYZcf0D_m2zu9PSlV5IYBJOnvc9k5OconhN8JIwTj7d-imMql-u_AhLjEVJef2kOCSC0UVNMXv6YH1QvIjxFuOKNXX9vDigJacN5fyw-HMJK-UC8hZF6AYYk-pRmy2RAQs6oSm6sUNXPsf7Nbp2eXa_waDkYpwAwdi5ESDkyFbVBWUTatdIIe2HNu8ZtIJgs40fcwowGzs1GqSnPk0BUFzHBMPL4plVfYRX83xUXH35fHX6bXF-8fXs9OR8oWtB06JluqWiUoZDa1legBAUKt0opbC2TatrMEwYTAwFJUhNLLamaRnn1paaHRVvd7ar3kc5lzBKUpGKCsJrkomzHWG8upWr4AYV1tIrJ7cBHzqpQnK6B0loVbOWVXWpSclsLSpbQgP5gxmxDctex3O2qR3A6FzdoPo90_2d0d3Izv-UTDQloTwbfJgNgv8xQUxycFFD36sR_LT975pTgTnN6Lt_0MdPN1Odygdwo_U5r96YyhPGq6phpcCZWj5C5WFgcDpfs3U5vif4uCfITIJfqVNTjPLs--X_sxfX--z7B-wNqD7dRN9PKT-muA-WO1AHH2MAe19kguWmXe6qITftIud2ybI3Dy_oXnTXH-wvp7sSwg</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Wang, Lin</creator><creator>Ma, Xiang-Yu</creator><creator>Zhang, Yang</creator><creator>Feng, Ya-Fei</creator><creator>Li, Xiang</creator><creator>Hu, Yun-Yu</creator><creator>Wang, Zhen</creator><creator>Ma, Zhen-Sheng</creator><creator>Lei, Wei</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140401</creationdate><title>Repair of segmental bone defect using Totally Vitalized tissue engineered bone graft by a combined perfusion seeding and culture system</title><author>Wang, Lin ; 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Based on this strategy, we proposed the "Totally Vitalized TEBG" (TV-TEBG) which was characterized by abundant and homogenously distributed cells with enhanced cell proliferation and differentiation and further investigated its biological performance in repairing segmental bone defect. In this study, we constructed the TV-TEBG with the combination of customized flow perfusion seeding/culture system and β-tricalcium phosphate (β-TCP) scaffold fabricated by Rapid Prototyping (RP) technique. We systemically compared three kinds of TEBG constructed by perfusion seeding and perfusion culture (PSPC) method, static seeding and perfusion culture (SSPC) method, and static seeding and static culture (SSSC) method for their in vitro performance and bone defect healing efficacy with a rabbit model. Our study has demonstrated that TEBG constructed by PSPC method exhibited better biological properties with higher daily D-glucose consumption, increased cell proliferation and differentiation, and better cell distribution, indicating the successful construction of TV-TEBG. After implanted into rabbit radius defects for 12 weeks, PSPC group exerted higher X-ray score close to autograft, much greater mechanical property evidenced by the biomechanical testing and significantly higher new bone formation as shown by histological analysis compared with the other two groups, and eventually obtained favorable healing efficacy of the segmental bone defect that was the closest to autograft transplantation. This study demonstrated the feasibility of TV-TEBG construction with combination of perfusion seeding, perfusion culture and RP technique which exerted excellent biological properties. The application of TV-TEBG may become a preferred candidate for segmental bone defect repair in orthopedic and maxillofacial fields.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24728277</pmid><doi>10.1371/journal.pone.0094276</doi><oa>free_for_read</oa></addata></record>
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subjects Alkaline Phosphatase - metabolism
Animals
Biocompatibility
Bioengineering
Biological properties
Biology and Life Sciences
Biomechanical Phenomena - drug effects
Biomechanics
Biomedical materials
Bioreactors
Bone diseases
Bone grafts
Bone growth
Bone healing
Bone marrow
Bone Regeneration - drug effects
Bone Transplantation
Bone-grafting
Bones
Calcium phosphates
Calcium Phosphates - pharmacology
Care and treatment
Cell adhesion & migration
Cell culture
Cell growth
Cell proliferation
Cell Survival - drug effects
Compressive Strength - drug effects
Construction
Construction methods
Defects
Design
Diagnosis
Differentiation
Engineering and Technology
Feasibility studies
Fluorescence
Fluorescent Dyes - metabolism
Glucose
Glucose - metabolism
Grafting
Healing
Hydroxyapatite
Implants, Experimental
In vitro methods and tests
Maxillofacial
Medicine and Health Sciences
Methods
Morphology
Orthopedics
Osteoblasts
Osteoblasts - cytology
Osteoblasts - drug effects
Osteoblasts - enzymology
Osteogenesis
Perfusion
Phosphates
Physiological aspects
Rabbits
Radius
Radius - diagnostic imaging
Radius - drug effects
Radius - pathology
Radius - surgery
Rapid prototyping
Repair
Shear stress
Skin & tissue grafts
Staining and Labeling
Stem cells
Studies
Time Factors
Tissue Culture Techniques
Tissue engineering
Tissue Engineering - methods
Tissue Scaffolds - chemistry
Transplantation
Tricalcium phosphate
Wound Healing - drug effects
X-Ray Microtomography
title Repair of segmental bone defect using Totally Vitalized tissue engineered bone graft by a combined perfusion seeding and culture system
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