Fractionated human adipose tissue as a native biomaterial for the generation of a bone organ by endochondral ossification
[Display omitted] Many steps are required to generate bone through endochondral ossification with adipose mesenchymal stromal cells (ASC), from cell isolation to in vitro monolayer expansion, seeding into scaffolds, cartilaginous differentiation and in vivo remodeling. Moreover, monolayer expansion...
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creator | Guerrero, Julien Pigeot, Sebastien Müller, Judith Schaefer, Dirk J Martin, Ivan Scherberich, Arnaud |
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Many steps are required to generate bone through endochondral ossification with adipose mesenchymal stromal cells (ASC), from cell isolation to in vitro monolayer expansion, seeding into scaffolds, cartilaginous differentiation and in vivo remodeling. Moreover, monolayer expansion and passaging of ASC strongly decreases their differentiation potential. Here, we propose that adipose tissue itself can be used as scaffold for ASC expansion and endochondral ossification. Human liposuctions were fractionated and cultured for 3 weeks with proliferative medium in suspension. The resulting constructs, named Adiscaf, were compared to constructs generated with a previously developed, control approach, i.e. collagen sponges seeded with monolayer-expanded ASC. After 4 weeks of chondrogenic differentiation, Adiscaf contained cartilage tissue, characterized by glycosaminoglycans and collagen type II. After 2 additional weeks of hypertrophic differentiation, Adiscaf showed upregulation of hypertrophic markers at the gene expression and protein levels. After 8 weeks of in vivo implantation, Adiscaf resulted in ectopic bone tissue formation, including bone marrow elements. Adiscaf showed superior in vitro differentiation and in vivo performance as compared to the control paradigm involving isolation and monolayer expansion of ASC. This new paradigm exploits the physiological niche of adipose tissue and strongly suggests a higher functionality of cells inside adipose tissue after in vitro expansion. This study demonstrates that adult human adipose tissue used as a native construct can generate a bone organ by endochondral ossification. The concept could be exploited for the generation of osteogenic grafts for bone repair.
In this study we used adult human adipose tissue as scaffolding materials (called Adiscaf) to generate a bone organ by endochondral ossification. Adiscaf concept is based on the culture of adipose tissue cells inside their native microenvironment for the generation of osteogenic grafts for bone repair. This simplified approach overcomes several limitations linked to the current techniques in bone tissue engineering, such as isolation of cells and inadequate properties of the biomaterials used as scaffolds. In addition, the present paradigm proposes to exploit physiological niches in order to better maintain the functionality of cells during their in vitro expansion. This project not only has a scientific impact by evaluating the impact of |
doi_str_mv | 10.1016/j.actbio.2018.07.004 |
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Many steps are required to generate bone through endochondral ossification with adipose mesenchymal stromal cells (ASC), from cell isolation to in vitro monolayer expansion, seeding into scaffolds, cartilaginous differentiation and in vivo remodeling. Moreover, monolayer expansion and passaging of ASC strongly decreases their differentiation potential. Here, we propose that adipose tissue itself can be used as scaffold for ASC expansion and endochondral ossification. Human liposuctions were fractionated and cultured for 3 weeks with proliferative medium in suspension. The resulting constructs, named Adiscaf, were compared to constructs generated with a previously developed, control approach, i.e. collagen sponges seeded with monolayer-expanded ASC. After 4 weeks of chondrogenic differentiation, Adiscaf contained cartilage tissue, characterized by glycosaminoglycans and collagen type II. After 2 additional weeks of hypertrophic differentiation, Adiscaf showed upregulation of hypertrophic markers at the gene expression and protein levels. After 8 weeks of in vivo implantation, Adiscaf resulted in ectopic bone tissue formation, including bone marrow elements. Adiscaf showed superior in vitro differentiation and in vivo performance as compared to the control paradigm involving isolation and monolayer expansion of ASC. This new paradigm exploits the physiological niche of adipose tissue and strongly suggests a higher functionality of cells inside adipose tissue after in vitro expansion. This study demonstrates that adult human adipose tissue used as a native construct can generate a bone organ by endochondral ossification. The concept could be exploited for the generation of osteogenic grafts for bone repair.
In this study we used adult human adipose tissue as scaffolding materials (called Adiscaf) to generate a bone organ by endochondral ossification. Adiscaf concept is based on the culture of adipose tissue cells inside their native microenvironment for the generation of osteogenic grafts for bone repair. This simplified approach overcomes several limitations linked to the current techniques in bone tissue engineering, such as isolation of cells and inadequate properties of the biomaterials used as scaffolds. In addition, the present paradigm proposes to exploit physiological niches in order to better maintain the functionality of cells during their in vitro expansion. This project not only has a scientific impact by evaluating the impact of native physiological niches on the functionality and chondrogenic differentiation of mesenchymal progenitors but also a clinical impact to generate osteogenic grafts and/or osteoinductive materials for bone regeneration and repair.</description><identifier>ISSN: 1742-7061</identifier><identifier>EISSN: 1878-7568</identifier><identifier>DOI: 10.1016/j.actbio.2018.07.004</identifier><identifier>PMID: 30126590</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>3D microenvironment ; Adipose stem cells ; Adipose tissue ; Biocompatibility ; Biomaterials ; Biomedical materials ; Bone diseases ; Bone growth ; Bone healing ; Bone marrow ; Cartilage ; Chondrogenesis ; Collagen ; Collagen (type II) ; Differentiation ; Embryology ; Endochondral bone ; Endochondral ossification ; Expansion ; Gene expression ; Glycosaminoglycans ; Grafts ; Human adipose tissue ; Implantation ; Mesenchyme ; Monolayers ; Ossification ; Osteogenesis ; Proteins ; Reconstructive surgery ; Scaffolds ; Stem cells ; Stromal cells ; Surgical implants ; Tissue engineering ; Tissues</subject><ispartof>Acta biomaterialia, 2018-09, Vol.77, p.142-154</ispartof><rights>2018 Acta Materialia Inc.</rights><rights>Copyright © 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier BV Sep 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-56a5d7b09d1e3f92e59ebb8227a5682af8e381da981db610dfaf435f48b5c9b73</citedby><cites>FETCH-LOGICAL-c493t-56a5d7b09d1e3f92e59ebb8227a5682af8e381da981db610dfaf435f48b5c9b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1742706118303982$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30126590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guerrero, Julien</creatorcontrib><creatorcontrib>Pigeot, Sebastien</creatorcontrib><creatorcontrib>Müller, Judith</creatorcontrib><creatorcontrib>Schaefer, Dirk J</creatorcontrib><creatorcontrib>Martin, Ivan</creatorcontrib><creatorcontrib>Scherberich, Arnaud</creatorcontrib><title>Fractionated human adipose tissue as a native biomaterial for the generation of a bone organ by endochondral ossification</title><title>Acta biomaterialia</title><addtitle>Acta Biomater</addtitle><description>[Display omitted]
Many steps are required to generate bone through endochondral ossification with adipose mesenchymal stromal cells (ASC), from cell isolation to in vitro monolayer expansion, seeding into scaffolds, cartilaginous differentiation and in vivo remodeling. Moreover, monolayer expansion and passaging of ASC strongly decreases their differentiation potential. Here, we propose that adipose tissue itself can be used as scaffold for ASC expansion and endochondral ossification. Human liposuctions were fractionated and cultured for 3 weeks with proliferative medium in suspension. The resulting constructs, named Adiscaf, were compared to constructs generated with a previously developed, control approach, i.e. collagen sponges seeded with monolayer-expanded ASC. After 4 weeks of chondrogenic differentiation, Adiscaf contained cartilage tissue, characterized by glycosaminoglycans and collagen type II. After 2 additional weeks of hypertrophic differentiation, Adiscaf showed upregulation of hypertrophic markers at the gene expression and protein levels. After 8 weeks of in vivo implantation, Adiscaf resulted in ectopic bone tissue formation, including bone marrow elements. Adiscaf showed superior in vitro differentiation and in vivo performance as compared to the control paradigm involving isolation and monolayer expansion of ASC. This new paradigm exploits the physiological niche of adipose tissue and strongly suggests a higher functionality of cells inside adipose tissue after in vitro expansion. This study demonstrates that adult human adipose tissue used as a native construct can generate a bone organ by endochondral ossification. The concept could be exploited for the generation of osteogenic grafts for bone repair.
In this study we used adult human adipose tissue as scaffolding materials (called Adiscaf) to generate a bone organ by endochondral ossification. Adiscaf concept is based on the culture of adipose tissue cells inside their native microenvironment for the generation of osteogenic grafts for bone repair. This simplified approach overcomes several limitations linked to the current techniques in bone tissue engineering, such as isolation of cells and inadequate properties of the biomaterials used as scaffolds. In addition, the present paradigm proposes to exploit physiological niches in order to better maintain the functionality of cells during their in vitro expansion. This project not only has a scientific impact by evaluating the impact of native physiological niches on the functionality and chondrogenic differentiation of mesenchymal progenitors but also a clinical impact to generate osteogenic grafts and/or osteoinductive materials for bone regeneration and repair.</description><subject>3D microenvironment</subject><subject>Adipose stem cells</subject><subject>Adipose tissue</subject><subject>Biocompatibility</subject><subject>Biomaterials</subject><subject>Biomedical materials</subject><subject>Bone diseases</subject><subject>Bone growth</subject><subject>Bone healing</subject><subject>Bone marrow</subject><subject>Cartilage</subject><subject>Chondrogenesis</subject><subject>Collagen</subject><subject>Collagen (type II)</subject><subject>Differentiation</subject><subject>Embryology</subject><subject>Endochondral bone</subject><subject>Endochondral ossification</subject><subject>Expansion</subject><subject>Gene expression</subject><subject>Glycosaminoglycans</subject><subject>Grafts</subject><subject>Human adipose tissue</subject><subject>Implantation</subject><subject>Mesenchyme</subject><subject>Monolayers</subject><subject>Ossification</subject><subject>Osteogenesis</subject><subject>Proteins</subject><subject>Reconstructive surgery</subject><subject>Scaffolds</subject><subject>Stem cells</subject><subject>Stromal cells</subject><subject>Surgical implants</subject><subject>Tissue engineering</subject><subject>Tissues</subject><issn>1742-7061</issn><issn>1878-7568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kUuPFCEUhYnROC__gTEkbmZT5YV6QG1MzMRxTCZx46wJj8s0nS5ooWqS_vfS06MLF26AhO-cy-EQ8p5By4CNn7attosJqeXAZAuiBehfkXMmhWzEMMrX9Sx63ggY2Rm5KGUL0EnG5Vty1gHj4zDBOTnc5moTUtQLOrpZZx2pdmGfCtIllLIi1YVqWu_DE9I6b65kDnpHfcp02SB9xIhZHz1o8hU1KSJN-bE6mQPF6JLdpOhylaRSgg_2Gb4ib7zeFXz3sl-Sh9uvP2_umvsf377ffLlvbD91SzOMenDCwOQYdn7iOExojORc6BqSay-xpnJ6qosZGTivfd8NvpdmsJMR3SW5Pvnuc_q1YlnUHIrF3U5HTGtRHCbGexDjEf34D7pNa471dYozxsQAHe8q1Z8om2uejF7tc5h1PigG6liN2qpTNepYjQKhajVV9uHFfDUzur-iP11U4PMJwPobTwGzKjZgtOhCRrsol8L_J_wGdDqiqA</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Guerrero, Julien</creator><creator>Pigeot, Sebastien</creator><creator>Müller, Judith</creator><creator>Schaefer, Dirk J</creator><creator>Martin, Ivan</creator><creator>Scherberich, Arnaud</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20180901</creationdate><title>Fractionated human adipose tissue as a native biomaterial for the generation of a bone organ by endochondral ossification</title><author>Guerrero, Julien ; Pigeot, Sebastien ; Müller, Judith ; Schaefer, Dirk J ; Martin, Ivan ; Scherberich, Arnaud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-56a5d7b09d1e3f92e59ebb8227a5682af8e381da981db610dfaf435f48b5c9b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>3D microenvironment</topic><topic>Adipose stem cells</topic><topic>Adipose tissue</topic><topic>Biocompatibility</topic><topic>Biomaterials</topic><topic>Biomedical materials</topic><topic>Bone diseases</topic><topic>Bone growth</topic><topic>Bone healing</topic><topic>Bone marrow</topic><topic>Cartilage</topic><topic>Chondrogenesis</topic><topic>Collagen</topic><topic>Collagen (type II)</topic><topic>Differentiation</topic><topic>Embryology</topic><topic>Endochondral bone</topic><topic>Endochondral ossification</topic><topic>Expansion</topic><topic>Gene expression</topic><topic>Glycosaminoglycans</topic><topic>Grafts</topic><topic>Human adipose tissue</topic><topic>Implantation</topic><topic>Mesenchyme</topic><topic>Monolayers</topic><topic>Ossification</topic><topic>Osteogenesis</topic><topic>Proteins</topic><topic>Reconstructive surgery</topic><topic>Scaffolds</topic><topic>Stem cells</topic><topic>Stromal cells</topic><topic>Surgical implants</topic><topic>Tissue engineering</topic><topic>Tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerrero, Julien</creatorcontrib><creatorcontrib>Pigeot, Sebastien</creatorcontrib><creatorcontrib>Müller, Judith</creatorcontrib><creatorcontrib>Schaefer, Dirk J</creatorcontrib><creatorcontrib>Martin, Ivan</creatorcontrib><creatorcontrib>Scherberich, Arnaud</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Acta biomaterialia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guerrero, Julien</au><au>Pigeot, Sebastien</au><au>Müller, Judith</au><au>Schaefer, Dirk J</au><au>Martin, Ivan</au><au>Scherberich, Arnaud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fractionated human adipose tissue as a native biomaterial for the generation of a bone organ by endochondral ossification</atitle><jtitle>Acta biomaterialia</jtitle><addtitle>Acta Biomater</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>77</volume><spage>142</spage><epage>154</epage><pages>142-154</pages><issn>1742-7061</issn><eissn>1878-7568</eissn><abstract>[Display omitted]
Many steps are required to generate bone through endochondral ossification with adipose mesenchymal stromal cells (ASC), from cell isolation to in vitro monolayer expansion, seeding into scaffolds, cartilaginous differentiation and in vivo remodeling. Moreover, monolayer expansion and passaging of ASC strongly decreases their differentiation potential. Here, we propose that adipose tissue itself can be used as scaffold for ASC expansion and endochondral ossification. Human liposuctions were fractionated and cultured for 3 weeks with proliferative medium in suspension. The resulting constructs, named Adiscaf, were compared to constructs generated with a previously developed, control approach, i.e. collagen sponges seeded with monolayer-expanded ASC. After 4 weeks of chondrogenic differentiation, Adiscaf contained cartilage tissue, characterized by glycosaminoglycans and collagen type II. After 2 additional weeks of hypertrophic differentiation, Adiscaf showed upregulation of hypertrophic markers at the gene expression and protein levels. After 8 weeks of in vivo implantation, Adiscaf resulted in ectopic bone tissue formation, including bone marrow elements. Adiscaf showed superior in vitro differentiation and in vivo performance as compared to the control paradigm involving isolation and monolayer expansion of ASC. This new paradigm exploits the physiological niche of adipose tissue and strongly suggests a higher functionality of cells inside adipose tissue after in vitro expansion. This study demonstrates that adult human adipose tissue used as a native construct can generate a bone organ by endochondral ossification. The concept could be exploited for the generation of osteogenic grafts for bone repair.
In this study we used adult human adipose tissue as scaffolding materials (called Adiscaf) to generate a bone organ by endochondral ossification. Adiscaf concept is based on the culture of adipose tissue cells inside their native microenvironment for the generation of osteogenic grafts for bone repair. This simplified approach overcomes several limitations linked to the current techniques in bone tissue engineering, such as isolation of cells and inadequate properties of the biomaterials used as scaffolds. In addition, the present paradigm proposes to exploit physiological niches in order to better maintain the functionality of cells during their in vitro expansion. This project not only has a scientific impact by evaluating the impact of native physiological niches on the functionality and chondrogenic differentiation of mesenchymal progenitors but also a clinical impact to generate osteogenic grafts and/or osteoinductive materials for bone regeneration and repair.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30126590</pmid><doi>10.1016/j.actbio.2018.07.004</doi><tpages>13</tpages></addata></record> |
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subjects | 3D microenvironment Adipose stem cells Adipose tissue Biocompatibility Biomaterials Biomedical materials Bone diseases Bone growth Bone healing Bone marrow Cartilage Chondrogenesis Collagen Collagen (type II) Differentiation Embryology Endochondral bone Endochondral ossification Expansion Gene expression Glycosaminoglycans Grafts Human adipose tissue Implantation Mesenchyme Monolayers Ossification Osteogenesis Proteins Reconstructive surgery Scaffolds Stem cells Stromal cells Surgical implants Tissue engineering Tissues |
title | Fractionated human adipose tissue as a native biomaterial for the generation of a bone organ by endochondral ossification |
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