Optimized Allogenic Decellularized Meniscal Scaffold Modified by Collagen Affinity Stromal Cell–Derived Factor SDF1α for Meniscal Regeneration: A 6- and 12-Week Animal Study in a Rabbit Model
Background: Total meniscectomy for treating massive meniscal tears may lead to joint instability, cartilage degeneration, and even progressive osteoarthritis. The meniscal substitution strategies for advancing reconstruction of the meniscus deserve further investigation. Hypothesis: A decellularized...
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Veröffentlicht in: | The American journal of sports medicine 2024-01, Vol.52 (1), p.124-139 |
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creator | Zhang, Tao Shi, Xin Li, Muzhi Hu, Jianzhong Lu, Hongbin |
description | Background:
Total meniscectomy for treating massive meniscal tears may lead to joint instability, cartilage degeneration, and even progressive osteoarthritis. The meniscal substitution strategies for advancing reconstruction of the meniscus deserve further investigation.
Hypothesis:
A decellularized meniscal scaffold (DMS) modified with collagen affinity stromal cell–derived factor (C-SDF1α) may facilitate meniscal regeneration and protect cartilage from abrasion.
Study Design:
Controlled laboratory study.
Methods:
The authors first modified DMS with C-SDF1α to fabricate a new meniscal graft (DMS-CBD [collagen-binding domain]). Second, they performed in vitro studies to evaluate the release dynamics, biocompatibility, and differentiation inducibility (osteogenic, chondrogenic, and tenogenic differentiation) on human bone marrow mesenchymal stem cells. Using in vivo studies, they subjected rabbits that received medial meniscectomy to a transplantation procedure to implement their meniscal graft. At postoperative weeks 6 and 12, the meniscal regeneration outcomes and chondroprotective efficacy of the new meniscal graft were evaluated by macroscopic observation, histology, micromechanics, and immunohistochemistry tests.
Results:
In in vitro studies, the optimized DMS-CBD graft showed notable biocompatibility, releasing efficiency, and chondrogenic inducibility. In in vivo studies, the implanted DMS-CBD graft after total meniscectomy promoted the migration of cells and extracellular matrix deposition in transplantation and further facilitated meniscal regeneration and protected articular cartilage from degeneration.
Conclusion:
The new meniscal graft (DMS-CBD) accelerated extracellular matrix deposition and meniscal regeneration and protected articular cartilage from degeneration.
Clinical Relevance:
The results demonstrate that the DMS-CBD graft can serve as a potential meniscal substitution after meniscectomy. |
doi_str_mv | 10.1177/03635465231210950 |
format | Article |
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Total meniscectomy for treating massive meniscal tears may lead to joint instability, cartilage degeneration, and even progressive osteoarthritis. The meniscal substitution strategies for advancing reconstruction of the meniscus deserve further investigation.
Hypothesis:
A decellularized meniscal scaffold (DMS) modified with collagen affinity stromal cell–derived factor (C-SDF1α) may facilitate meniscal regeneration and protect cartilage from abrasion.
Study Design:
Controlled laboratory study.
Methods:
The authors first modified DMS with C-SDF1α to fabricate a new meniscal graft (DMS-CBD [collagen-binding domain]). Second, they performed in vitro studies to evaluate the release dynamics, biocompatibility, and differentiation inducibility (osteogenic, chondrogenic, and tenogenic differentiation) on human bone marrow mesenchymal stem cells. Using in vivo studies, they subjected rabbits that received medial meniscectomy to a transplantation procedure to implement their meniscal graft. At postoperative weeks 6 and 12, the meniscal regeneration outcomes and chondroprotective efficacy of the new meniscal graft were evaluated by macroscopic observation, histology, micromechanics, and immunohistochemistry tests.
Results:
In in vitro studies, the optimized DMS-CBD graft showed notable biocompatibility, releasing efficiency, and chondrogenic inducibility. In in vivo studies, the implanted DMS-CBD graft after total meniscectomy promoted the migration of cells and extracellular matrix deposition in transplantation and further facilitated meniscal regeneration and protected articular cartilage from degeneration.
Conclusion:
The new meniscal graft (DMS-CBD) accelerated extracellular matrix deposition and meniscal regeneration and protected articular cartilage from degeneration.
Clinical Relevance:
The results demonstrate that the DMS-CBD graft can serve as a potential meniscal substitution after meniscectomy.</description><identifier>ISSN: 0363-5465</identifier><identifier>EISSN: 1552-3365</identifier><identifier>DOI: 10.1177/03635465231210950</identifier><identifier>PMID: 38164676</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Biocompatibility ; Cartilage ; Collagen ; Extracellular matrix</subject><ispartof>The American journal of sports medicine, 2024-01, Vol.52 (1), p.124-139</ispartof><rights>2023 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c363t-3b1c7b2f310484f330a84656105758ba0b4e0cb9d0b05f29c42143f06f614f543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/03635465231210950$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/03635465231210950$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38164676$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Shi, Xin</creatorcontrib><creatorcontrib>Li, Muzhi</creatorcontrib><creatorcontrib>Hu, Jianzhong</creatorcontrib><creatorcontrib>Lu, Hongbin</creatorcontrib><title>Optimized Allogenic Decellularized Meniscal Scaffold Modified by Collagen Affinity Stromal Cell–Derived Factor SDF1α for Meniscal Regeneration: A 6- and 12-Week Animal Study in a Rabbit Model</title><title>The American journal of sports medicine</title><addtitle>Am J Sports Med</addtitle><description>Background:
Total meniscectomy for treating massive meniscal tears may lead to joint instability, cartilage degeneration, and even progressive osteoarthritis. The meniscal substitution strategies for advancing reconstruction of the meniscus deserve further investigation.
Hypothesis:
A decellularized meniscal scaffold (DMS) modified with collagen affinity stromal cell–derived factor (C-SDF1α) may facilitate meniscal regeneration and protect cartilage from abrasion.
Study Design:
Controlled laboratory study.
Methods:
The authors first modified DMS with C-SDF1α to fabricate a new meniscal graft (DMS-CBD [collagen-binding domain]). Second, they performed in vitro studies to evaluate the release dynamics, biocompatibility, and differentiation inducibility (osteogenic, chondrogenic, and tenogenic differentiation) on human bone marrow mesenchymal stem cells. Using in vivo studies, they subjected rabbits that received medial meniscectomy to a transplantation procedure to implement their meniscal graft. At postoperative weeks 6 and 12, the meniscal regeneration outcomes and chondroprotective efficacy of the new meniscal graft were evaluated by macroscopic observation, histology, micromechanics, and immunohistochemistry tests.
Results:
In in vitro studies, the optimized DMS-CBD graft showed notable biocompatibility, releasing efficiency, and chondrogenic inducibility. In in vivo studies, the implanted DMS-CBD graft after total meniscectomy promoted the migration of cells and extracellular matrix deposition in transplantation and further facilitated meniscal regeneration and protected articular cartilage from degeneration.
Conclusion:
The new meniscal graft (DMS-CBD) accelerated extracellular matrix deposition and meniscal regeneration and protected articular cartilage from degeneration.
Clinical Relevance:
The results demonstrate that the DMS-CBD graft can serve as a potential meniscal substitution after meniscectomy.</description><subject>Biocompatibility</subject><subject>Cartilage</subject><subject>Collagen</subject><subject>Extracellular matrix</subject><issn>0363-5465</issn><issn>1552-3365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kcFu1DAQhi0EokvhAbggS1x6SfHEsZPlFu2yLVJRpS6IY2Q7NnLxxouTIG1PfQeepK_AA_AQfRImbCkSCPlga-ab3zPzE_Ic2DFAWb5iXHJRSJFzyIHNBXtAZiBEnnEuxUMym_LZBByQJ31_yRiDUlaPyQGvQBaylDPy_Xw7-I2_si2tQ4ifbOcNXVpjQxiDSr8S7zDYGxXo2ijnYsBIbL3zmNI7uoghKKyjtXO-88OOrocUN4gvUOT2-tvSJv8V2ZUyQ0x0vVzBjxvq8HkvfGFRwCY1-Ni9pjWVGVVdSyHPPlr7mdadn_TWw9juqO-oohdKaz9MfdjwlDxyKvT22d19SD6s3rxfnGZn5ydvF_VZZnANQ8Y1mFLnjgMrqsJxzlSFq5HARCkqrZguLDN63jLNhMvnpsih4I5JJ6FwouCH5Givu03xy2j7odlg9zij6mwc-yafs-kAZ4i-_Au9jGPqsDukQFZlVVUlUrCnTIp9n6xrtgkHTbsGWDMZ3PxjMNa8uFMe9ca29xW_HUXgeA_0aMqfb_-v-BOF2K3R</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Zhang, Tao</creator><creator>Shi, Xin</creator><creator>Li, Muzhi</creator><creator>Hu, Jianzhong</creator><creator>Lu, Hongbin</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TS</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>202401</creationdate><title>Optimized Allogenic Decellularized Meniscal Scaffold Modified by Collagen Affinity Stromal Cell–Derived Factor SDF1α for Meniscal Regeneration: A 6- and 12-Week Animal Study in a Rabbit Model</title><author>Zhang, Tao ; Shi, Xin ; Li, Muzhi ; Hu, Jianzhong ; Lu, Hongbin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-3b1c7b2f310484f330a84656105758ba0b4e0cb9d0b05f29c42143f06f614f543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biocompatibility</topic><topic>Cartilage</topic><topic>Collagen</topic><topic>Extracellular matrix</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Tao</creatorcontrib><creatorcontrib>Shi, Xin</creatorcontrib><creatorcontrib>Li, Muzhi</creatorcontrib><creatorcontrib>Hu, Jianzhong</creatorcontrib><creatorcontrib>Lu, Hongbin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Physical Education Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of sports medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Tao</au><au>Shi, Xin</au><au>Li, Muzhi</au><au>Hu, Jianzhong</au><au>Lu, Hongbin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimized Allogenic Decellularized Meniscal Scaffold Modified by Collagen Affinity Stromal Cell–Derived Factor SDF1α for Meniscal Regeneration: A 6- and 12-Week Animal Study in a Rabbit Model</atitle><jtitle>The American journal of sports medicine</jtitle><addtitle>Am J Sports Med</addtitle><date>2024-01</date><risdate>2024</risdate><volume>52</volume><issue>1</issue><spage>124</spage><epage>139</epage><pages>124-139</pages><issn>0363-5465</issn><eissn>1552-3365</eissn><abstract>Background:
Total meniscectomy for treating massive meniscal tears may lead to joint instability, cartilage degeneration, and even progressive osteoarthritis. The meniscal substitution strategies for advancing reconstruction of the meniscus deserve further investigation.
Hypothesis:
A decellularized meniscal scaffold (DMS) modified with collagen affinity stromal cell–derived factor (C-SDF1α) may facilitate meniscal regeneration and protect cartilage from abrasion.
Study Design:
Controlled laboratory study.
Methods:
The authors first modified DMS with C-SDF1α to fabricate a new meniscal graft (DMS-CBD [collagen-binding domain]). Second, they performed in vitro studies to evaluate the release dynamics, biocompatibility, and differentiation inducibility (osteogenic, chondrogenic, and tenogenic differentiation) on human bone marrow mesenchymal stem cells. Using in vivo studies, they subjected rabbits that received medial meniscectomy to a transplantation procedure to implement their meniscal graft. At postoperative weeks 6 and 12, the meniscal regeneration outcomes and chondroprotective efficacy of the new meniscal graft were evaluated by macroscopic observation, histology, micromechanics, and immunohistochemistry tests.
Results:
In in vitro studies, the optimized DMS-CBD graft showed notable biocompatibility, releasing efficiency, and chondrogenic inducibility. In in vivo studies, the implanted DMS-CBD graft after total meniscectomy promoted the migration of cells and extracellular matrix deposition in transplantation and further facilitated meniscal regeneration and protected articular cartilage from degeneration.
Conclusion:
The new meniscal graft (DMS-CBD) accelerated extracellular matrix deposition and meniscal regeneration and protected articular cartilage from degeneration.
Clinical Relevance:
The results demonstrate that the DMS-CBD graft can serve as a potential meniscal substitution after meniscectomy.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>38164676</pmid><doi>10.1177/03635465231210950</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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source | SAGE Complete A-Z List; Alma/SFX Local Collection |
subjects | Biocompatibility Cartilage Collagen Extracellular matrix |
title | Optimized Allogenic Decellularized Meniscal Scaffold Modified by Collagen Affinity Stromal Cell–Derived Factor SDF1α for Meniscal Regeneration: A 6- and 12-Week Animal Study in a Rabbit Model |
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