Evaluation of an Autologous Bone Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffold in a Rabbit and Minipig Model of Cartilage Repair

BACKGROUND This study aimed to evaluate an autologous bone mesenchymal stem cell (MSC)-derived extracellular matrix (ECM) scaffold in two animal models of cartilage repair. MATERIAL AND METHODS A rabbit model (n=16) and a minipig model (n=8) of cartilage repair were created with cartilage defects of...

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Veröffentlicht in:Medical science monitor 2019-09, Vol.25, p.7342-7350
Hauptverfasser: Tang, Cheng, Jin, Chengzhe, Li, Xiangquan, Li, Jiayi, Du, Xiaotao, Yan, Chao, Lu, Shanshan, Wei, Bo, Xu, Yan, Wang, Liming
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container_end_page 7350
container_issue
container_start_page 7342
container_title Medical science monitor
container_volume 25
creator Tang, Cheng
Jin, Chengzhe
Li, Xiangquan
Li, Jiayi
Du, Xiaotao
Yan, Chao
Lu, Shanshan
Wei, Bo
Xu, Yan
Wang, Liming
description BACKGROUND This study aimed to evaluate an autologous bone mesenchymal stem cell (MSC)-derived extracellular matrix (ECM) scaffold in two animal models of cartilage repair. MATERIAL AND METHODS A rabbit model (n=16) and a minipig model (n=8) of cartilage repair were created with cartilage defects of the knee joints treated with bone marrow stimulation (BMS). In the ECM group, autologous bone MSC-derived ECM scaffolds were implanted into the cartilage defects after bone marrow stimulation. In the BMS group, the cartilage defects were treated by bone marrow stimulation only. The renewal capacity of bone MSCs was measured with a colony-forming unit fibroblast (CFU-F) in vitro assay. The extent of cartilage repair was as-sessed at 6 months after surgery. RESULTS In the rabbit model, the macroscopic appearance of the exudate of the healing wounds in the ECM group showed less fibrosis, and the histology showed more evenly distributed chondrocytes compared with the BMS group. The CFU-F assay showed that the number of bone MSCs in the ECM group was approximately was twice that of the BMS group. In the minipig model, the macroscopic appearance and magnetic resonance imaging (MRI) findings of the ECM group were improved when compared with the BMS group. The repaired tissue in ECM group had similar histological characteristics and biochemical content to normal hyaline cartilage. CONCLUSIONS In two animal models of knee joint cartilage repair, the use of an ECM scaffold increased the number of bone MSCs and improved the extent of cartilage repair.
doi_str_mv 10.12659/MSM.916481
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MATERIAL AND METHODS A rabbit model (n=16) and a minipig model (n=8) of cartilage repair were created with cartilage defects of the knee joints treated with bone marrow stimulation (BMS). In the ECM group, autologous bone MSC-derived ECM scaffolds were implanted into the cartilage defects after bone marrow stimulation. In the BMS group, the cartilage defects were treated by bone marrow stimulation only. The renewal capacity of bone MSCs was measured with a colony-forming unit fibroblast (CFU-F) in vitro assay. The extent of cartilage repair was as-sessed at 6 months after surgery. RESULTS In the rabbit model, the macroscopic appearance of the exudate of the healing wounds in the ECM group showed less fibrosis, and the histology showed more evenly distributed chondrocytes compared with the BMS group. The CFU-F assay showed that the number of bone MSCs in the ECM group was approximately was twice that of the BMS group. In the minipig model, the macroscopic appearance and magnetic resonance imaging (MRI) findings of the ECM group were improved when compared with the BMS group. The repaired tissue in ECM group had similar histological characteristics and biochemical content to normal hyaline cartilage. CONCLUSIONS In two animal models of knee joint cartilage repair, the use of an ECM scaffold increased the number of bone MSCs and improved the extent of cartilage repair.</description><identifier>ISSN: 1643-3750</identifier><identifier>ISSN: 1234-1010</identifier><identifier>EISSN: 1643-3750</identifier><identifier>DOI: 10.12659/MSM.916481</identifier><identifier>PMID: 31566195</identifier><language>eng</language><publisher>United States: International Scientific Literature, Inc</publisher><subject>Animal Study ; Animals ; Bone and Bones ; Bone Marrow ; Bone Matrix - pathology ; Cartilage, Articular - metabolism ; Cartilage, Articular - pathology ; Cells, Cultured ; Chondrocytes ; Extracellular Matrix ; Knee Joint - surgery ; Mesenchymal Stem Cell Transplantation - methods ; Mesenchymal Stem Cells - metabolism ; Models, Animal ; Rabbits ; Swine ; Swine, Miniature ; Tissue Engineering - methods ; Tissue Scaffolds</subject><ispartof>Medical science monitor, 2019-09, Vol.25, p.7342-7350</ispartof><rights>Med Sci Monit, 2019 2019</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-90fdba7e54761ec59f3b8316c3e413518b52c87f6d9bf514a74106045288733c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784685/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6784685/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31566195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tang, Cheng</creatorcontrib><creatorcontrib>Jin, Chengzhe</creatorcontrib><creatorcontrib>Li, Xiangquan</creatorcontrib><creatorcontrib>Li, Jiayi</creatorcontrib><creatorcontrib>Du, Xiaotao</creatorcontrib><creatorcontrib>Yan, Chao</creatorcontrib><creatorcontrib>Lu, Shanshan</creatorcontrib><creatorcontrib>Wei, Bo</creatorcontrib><creatorcontrib>Xu, Yan</creatorcontrib><creatorcontrib>Wang, Liming</creatorcontrib><title>Evaluation of an Autologous Bone Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffold in a Rabbit and Minipig Model of Cartilage Repair</title><title>Medical science monitor</title><addtitle>Med Sci Monit</addtitle><description>BACKGROUND This study aimed to evaluate an autologous bone mesenchymal stem cell (MSC)-derived extracellular matrix (ECM) scaffold in two animal models of cartilage repair. MATERIAL AND METHODS A rabbit model (n=16) and a minipig model (n=8) of cartilage repair were created with cartilage defects of the knee joints treated with bone marrow stimulation (BMS). In the ECM group, autologous bone MSC-derived ECM scaffolds were implanted into the cartilage defects after bone marrow stimulation. In the BMS group, the cartilage defects were treated by bone marrow stimulation only. The renewal capacity of bone MSCs was measured with a colony-forming unit fibroblast (CFU-F) in vitro assay. The extent of cartilage repair was as-sessed at 6 months after surgery. RESULTS In the rabbit model, the macroscopic appearance of the exudate of the healing wounds in the ECM group showed less fibrosis, and the histology showed more evenly distributed chondrocytes compared with the BMS group. The CFU-F assay showed that the number of bone MSCs in the ECM group was approximately was twice that of the BMS group. In the minipig model, the macroscopic appearance and magnetic resonance imaging (MRI) findings of the ECM group were improved when compared with the BMS group. The repaired tissue in ECM group had similar histological characteristics and biochemical content to normal hyaline cartilage. CONCLUSIONS In two animal models of knee joint cartilage repair, the use of an ECM scaffold increased the number of bone MSCs and improved the extent of cartilage repair.</description><subject>Animal Study</subject><subject>Animals</subject><subject>Bone and Bones</subject><subject>Bone Marrow</subject><subject>Bone Matrix - pathology</subject><subject>Cartilage, Articular - metabolism</subject><subject>Cartilage, Articular - pathology</subject><subject>Cells, Cultured</subject><subject>Chondrocytes</subject><subject>Extracellular Matrix</subject><subject>Knee Joint - surgery</subject><subject>Mesenchymal Stem Cell Transplantation - methods</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Models, Animal</subject><subject>Rabbits</subject><subject>Swine</subject><subject>Swine, Miniature</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds</subject><issn>1643-3750</issn><issn>1234-1010</issn><issn>1643-3750</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1v1DAQjRCIlsKJO_IRCaX4O84FqV22gNQIqQtna-JMtkZOvNjJqv0T_OambKnKaUYzT-_NvFcUbxk9ZVyr-mOzaU5rpqVhz4rjpYpSVIo-f9IfFa9y_kUpN5qql8WRYEprVqvj4s96D2GGyceRxJ7ASM7mKYa4jXMm53FE0mDG0V3fDhDIZsKBrDCE8jMmv8eOrG-mBG6ZzAESaWBK_oZsHPR9DB3xIwFyBW3rp4W6I40f_c5vSRM7DPd6K0iTD7BFcoU78Ol18aKHkPHNQz0pfl6sf6y-lpffv3xbnV2WTnIxlTXtuxYqVLLSDJ2qe9EawbQTKJlQzLSKO1P1uqvbXjEJlWRUU6m4MZUQTpwUnw68u7kdsHM4Lm8Eu0t-gHRrI3j7_2b013Yb91ZXRmqjFoL3DwQp_p4xT3bw-d4HGHGxznJe11KaivMF-uEAdSnmnLB_lGHU_k3QLgnaQ4IL-t3Tyx6x_yITdy66mAY</recordid><startdate>20190930</startdate><enddate>20190930</enddate><creator>Tang, Cheng</creator><creator>Jin, Chengzhe</creator><creator>Li, Xiangquan</creator><creator>Li, Jiayi</creator><creator>Du, Xiaotao</creator><creator>Yan, Chao</creator><creator>Lu, Shanshan</creator><creator>Wei, Bo</creator><creator>Xu, Yan</creator><creator>Wang, Liming</creator><general>International Scientific Literature, Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190930</creationdate><title>Evaluation of an Autologous Bone Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffold in a Rabbit and Minipig Model of Cartilage Repair</title><author>Tang, Cheng ; Jin, Chengzhe ; Li, Xiangquan ; Li, Jiayi ; Du, Xiaotao ; Yan, Chao ; Lu, Shanshan ; Wei, Bo ; Xu, Yan ; Wang, Liming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-90fdba7e54761ec59f3b8316c3e413518b52c87f6d9bf514a74106045288733c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animal Study</topic><topic>Animals</topic><topic>Bone and Bones</topic><topic>Bone Marrow</topic><topic>Bone Matrix - pathology</topic><topic>Cartilage, Articular - metabolism</topic><topic>Cartilage, Articular - pathology</topic><topic>Cells, Cultured</topic><topic>Chondrocytes</topic><topic>Extracellular Matrix</topic><topic>Knee Joint - surgery</topic><topic>Mesenchymal Stem Cell Transplantation - methods</topic><topic>Mesenchymal Stem Cells - metabolism</topic><topic>Models, Animal</topic><topic>Rabbits</topic><topic>Swine</topic><topic>Swine, Miniature</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds</topic><toplevel>online_resources</toplevel><creatorcontrib>Tang, Cheng</creatorcontrib><creatorcontrib>Jin, Chengzhe</creatorcontrib><creatorcontrib>Li, Xiangquan</creatorcontrib><creatorcontrib>Li, Jiayi</creatorcontrib><creatorcontrib>Du, Xiaotao</creatorcontrib><creatorcontrib>Yan, Chao</creatorcontrib><creatorcontrib>Lu, Shanshan</creatorcontrib><creatorcontrib>Wei, Bo</creatorcontrib><creatorcontrib>Xu, Yan</creatorcontrib><creatorcontrib>Wang, Liming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medical science monitor</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tang, Cheng</au><au>Jin, Chengzhe</au><au>Li, Xiangquan</au><au>Li, Jiayi</au><au>Du, Xiaotao</au><au>Yan, Chao</au><au>Lu, Shanshan</au><au>Wei, Bo</au><au>Xu, Yan</au><au>Wang, Liming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of an Autologous Bone Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffold in a Rabbit and Minipig Model of Cartilage Repair</atitle><jtitle>Medical science monitor</jtitle><addtitle>Med Sci Monit</addtitle><date>2019-09-30</date><risdate>2019</risdate><volume>25</volume><spage>7342</spage><epage>7350</epage><pages>7342-7350</pages><issn>1643-3750</issn><issn>1234-1010</issn><eissn>1643-3750</eissn><abstract>BACKGROUND This study aimed to evaluate an autologous bone mesenchymal stem cell (MSC)-derived extracellular matrix (ECM) scaffold in two animal models of cartilage repair. MATERIAL AND METHODS A rabbit model (n=16) and a minipig model (n=8) of cartilage repair were created with cartilage defects of the knee joints treated with bone marrow stimulation (BMS). In the ECM group, autologous bone MSC-derived ECM scaffolds were implanted into the cartilage defects after bone marrow stimulation. In the BMS group, the cartilage defects were treated by bone marrow stimulation only. The renewal capacity of bone MSCs was measured with a colony-forming unit fibroblast (CFU-F) in vitro assay. The extent of cartilage repair was as-sessed at 6 months after surgery. RESULTS In the rabbit model, the macroscopic appearance of the exudate of the healing wounds in the ECM group showed less fibrosis, and the histology showed more evenly distributed chondrocytes compared with the BMS group. The CFU-F assay showed that the number of bone MSCs in the ECM group was approximately was twice that of the BMS group. In the minipig model, the macroscopic appearance and magnetic resonance imaging (MRI) findings of the ECM group were improved when compared with the BMS group. The repaired tissue in ECM group had similar histological characteristics and biochemical content to normal hyaline cartilage. CONCLUSIONS In two animal models of knee joint cartilage repair, the use of an ECM scaffold increased the number of bone MSCs and improved the extent of cartilage repair.</abstract><cop>United States</cop><pub>International Scientific Literature, Inc</pub><pmid>31566195</pmid><doi>10.12659/MSM.916481</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Animal Study
Animals
Bone and Bones
Bone Marrow
Bone Matrix - pathology
Cartilage, Articular - metabolism
Cartilage, Articular - pathology
Cells, Cultured
Chondrocytes
Extracellular Matrix
Knee Joint - surgery
Mesenchymal Stem Cell Transplantation - methods
Mesenchymal Stem Cells - metabolism
Models, Animal
Rabbits
Swine
Swine, Miniature
Tissue Engineering - methods
Tissue Scaffolds
title Evaluation of an Autologous Bone Mesenchymal Stem Cell-Derived Extracellular Matrix Scaffold in a Rabbit and Minipig Model of Cartilage Repair
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