Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model
Background: Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved men...
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Veröffentlicht in: | The American journal of sports medicine 2019-09, Vol.47 (11), p.2596-2607 |
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creator | Nakagawa, Yusuke Fortier, Lisa A. Mao, Jeremy J. Lee, Chang Hun Goodale, Margaret B. Koff, Matthew F. Uppstrom, Tyler J. Croen, Brett Wada, Susumu Carballo, Camila B. Potter, Hollis G. Rodeo, Scott A. |
description | Background:
Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI).
Purpose:
To evaluate long-term outcome of meniscal replacement with growth factor–laden poly-ε-caprolactone (PCL) scaffolds.
Study Design:
Controlled laboratory study.
Methods:
Anatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups.
Results:
Remnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%).
Conclusion:
Previously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion.
Clinical Relevance:
A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menis |
doi_str_mv | 10.1177/0363546519865513 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7422478</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_0363546519865513</sage_id><sourcerecordid>2269405128</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3773-c2f4687613b93a47405f2506fd768bf030c84cb95bd093af678adb3f863382283</originalsourceid><addsrcrecordid>eNp1ksFu1DAQhi0EotvCnROyxIVLwPYkdvaChFbdBWmrIrqIY-Q49taVYxc7WcSNd-iDIPEgPARPgsO2BSpxsqz_m39mfhuhJ5S8oFSIlwQ4VCWv6LzmVUXhHprRqmIFAK_uo9kkF5N-gA5TuiCEUMHrh-gAKEwFZIa-rYPfFoOOPT7eSTfKwQaPg8En2tukpMMbm9Ko8TLEfi9aj6HobK99ylfpfn69ehetH3SHz5Q0Jrgu4Y92OMdn-tOo_WCzy3vttEx6cl4E77Ua7E7feK9i-JzxpVRDiFj6Dm9Wy-LHd5h6SY9Pd9ZrfBI67R6hB0a6pB9fn0fow_J4s3hTrE9Xbxev14UCIaBQzJS8FpxCOwdZipJUhlWEmy4H0BoCRNWlaudV25EMGC5q2bVgag5QM1bDEXq1970c2153Kq8RpWsuo-1l_NIEaZt_FW_Pm23YNaJkrBSTwfNrgxhyCmlo-pyndk56HcbUMMbneSr6u9ezO-hFGGNOdqJqmAOjwDJF9pSKIaWoze0wlDTTb2ju_oZc8vTvJW4Lbp4_A8UeSHKr_3T9r-Evfce_Xw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2283932132</pqid></control><display><type>article</type><title>Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model</title><source>Access via SAGE</source><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Nakagawa, Yusuke ; Fortier, Lisa A. ; Mao, Jeremy J. ; Lee, Chang Hun ; Goodale, Margaret B. ; Koff, Matthew F. ; Uppstrom, Tyler J. ; Croen, Brett ; Wada, Susumu ; Carballo, Camila B. ; Potter, Hollis G. ; Rodeo, Scott A.</creator><creatorcontrib>Nakagawa, Yusuke ; Fortier, Lisa A. ; Mao, Jeremy J. ; Lee, Chang Hun ; Goodale, Margaret B. ; Koff, Matthew F. ; Uppstrom, Tyler J. ; Croen, Brett ; Wada, Susumu ; Carballo, Camila B. ; Potter, Hollis G. ; Rodeo, Scott A.</creatorcontrib><description>Background:
Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI).
Purpose:
To evaluate long-term outcome of meniscal replacement with growth factor–laden poly-ε-caprolactone (PCL) scaffolds.
Study Design:
Controlled laboratory study.
Methods:
Anatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups.
Results:
Remnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%).
Conclusion:
Previously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion.
Clinical Relevance:
A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menisci could be printed and available for off-the-shelf applications. Based on the 1-year duration of the study, the approach appears to be promising for meniscal regeneration in humans.</description><identifier>ISSN: 0363-5465</identifier><identifier>EISSN: 1552-3365</identifier><identifier>DOI: 10.1177/0363546519865513</identifier><identifier>PMID: 31386550</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Connective Tissue Growth Factor - metabolism ; Growth factors ; Histology ; Meniscus - surgery ; Models, Animal ; NMR ; Nuclear magnetic resonance ; Printing, Three-Dimensional - statistics & numerical data ; Sheep ; Sports medicine ; Tissue Scaffolds - statistics & numerical data ; Transforming Growth Factor beta3 - metabolism</subject><ispartof>The American journal of sports medicine, 2019-09, Vol.47 (11), p.2596-2607</ispartof><rights>2019 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3773-c2f4687613b93a47405f2506fd768bf030c84cb95bd093af678adb3f863382283</citedby><cites>FETCH-LOGICAL-c3773-c2f4687613b93a47405f2506fd768bf030c84cb95bd093af678adb3f863382283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0363546519865513$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0363546519865513$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31386550$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakagawa, Yusuke</creatorcontrib><creatorcontrib>Fortier, Lisa A.</creatorcontrib><creatorcontrib>Mao, Jeremy J.</creatorcontrib><creatorcontrib>Lee, Chang Hun</creatorcontrib><creatorcontrib>Goodale, Margaret B.</creatorcontrib><creatorcontrib>Koff, Matthew F.</creatorcontrib><creatorcontrib>Uppstrom, Tyler J.</creatorcontrib><creatorcontrib>Croen, Brett</creatorcontrib><creatorcontrib>Wada, Susumu</creatorcontrib><creatorcontrib>Carballo, Camila B.</creatorcontrib><creatorcontrib>Potter, Hollis G.</creatorcontrib><creatorcontrib>Rodeo, Scott A.</creatorcontrib><title>Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model</title><title>The American journal of sports medicine</title><addtitle>Am J Sports Med</addtitle><description>Background:
Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI).
Purpose:
To evaluate long-term outcome of meniscal replacement with growth factor–laden poly-ε-caprolactone (PCL) scaffolds.
Study Design:
Controlled laboratory study.
Methods:
Anatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups.
Results:
Remnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%).
Conclusion:
Previously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion.
Clinical Relevance:
A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menisci could be printed and available for off-the-shelf applications. Based on the 1-year duration of the study, the approach appears to be promising for meniscal regeneration in humans.</description><subject>Animals</subject><subject>Connective Tissue Growth Factor - metabolism</subject><subject>Growth factors</subject><subject>Histology</subject><subject>Meniscus - surgery</subject><subject>Models, Animal</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Printing, Three-Dimensional - statistics & numerical data</subject><subject>Sheep</subject><subject>Sports medicine</subject><subject>Tissue Scaffolds - statistics & numerical data</subject><subject>Transforming Growth Factor beta3 - metabolism</subject><issn>0363-5465</issn><issn>1552-3365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1ksFu1DAQhi0EotvCnROyxIVLwPYkdvaChFbdBWmrIrqIY-Q49taVYxc7WcSNd-iDIPEgPARPgsO2BSpxsqz_m39mfhuhJ5S8oFSIlwQ4VCWv6LzmVUXhHprRqmIFAK_uo9kkF5N-gA5TuiCEUMHrh-gAKEwFZIa-rYPfFoOOPT7eSTfKwQaPg8En2tukpMMbm9Ko8TLEfi9aj6HobK99ylfpfn69ehetH3SHz5Q0Jrgu4Y92OMdn-tOo_WCzy3vttEx6cl4E77Ua7E7feK9i-JzxpVRDiFj6Dm9Wy-LHd5h6SY9Pd9ZrfBI67R6hB0a6pB9fn0fow_J4s3hTrE9Xbxev14UCIaBQzJS8FpxCOwdZipJUhlWEmy4H0BoCRNWlaudV25EMGC5q2bVgag5QM1bDEXq1970c2153Kq8RpWsuo-1l_NIEaZt_FW_Pm23YNaJkrBSTwfNrgxhyCmlo-pyndk56HcbUMMbneSr6u9ezO-hFGGNOdqJqmAOjwDJF9pSKIaWoze0wlDTTb2ju_oZc8vTvJW4Lbp4_A8UeSHKr_3T9r-Evfce_Xw</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Nakagawa, Yusuke</creator><creator>Fortier, Lisa A.</creator><creator>Mao, Jeremy J.</creator><creator>Lee, Chang Hun</creator><creator>Goodale, Margaret B.</creator><creator>Koff, Matthew F.</creator><creator>Uppstrom, Tyler J.</creator><creator>Croen, Brett</creator><creator>Wada, Susumu</creator><creator>Carballo, Camila B.</creator><creator>Potter, Hollis G.</creator><creator>Rodeo, Scott A.</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>7TS</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190901</creationdate><title>Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model</title><author>Nakagawa, Yusuke ; Fortier, Lisa A. ; Mao, Jeremy J. ; Lee, Chang Hun ; Goodale, Margaret B. ; Koff, Matthew F. ; Uppstrom, Tyler J. ; Croen, Brett ; Wada, Susumu ; Carballo, Camila B. ; Potter, Hollis G. ; Rodeo, Scott A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3773-c2f4687613b93a47405f2506fd768bf030c84cb95bd093af678adb3f863382283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Connective Tissue Growth Factor - metabolism</topic><topic>Growth factors</topic><topic>Histology</topic><topic>Meniscus - surgery</topic><topic>Models, Animal</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Printing, Three-Dimensional - statistics & numerical data</topic><topic>Sheep</topic><topic>Sports medicine</topic><topic>Tissue Scaffolds - statistics & numerical data</topic><topic>Transforming Growth Factor beta3 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakagawa, Yusuke</creatorcontrib><creatorcontrib>Fortier, Lisa A.</creatorcontrib><creatorcontrib>Mao, Jeremy J.</creatorcontrib><creatorcontrib>Lee, Chang Hun</creatorcontrib><creatorcontrib>Goodale, Margaret B.</creatorcontrib><creatorcontrib>Koff, Matthew F.</creatorcontrib><creatorcontrib>Uppstrom, Tyler J.</creatorcontrib><creatorcontrib>Croen, Brett</creatorcontrib><creatorcontrib>Wada, Susumu</creatorcontrib><creatorcontrib>Carballo, Camila B.</creatorcontrib><creatorcontrib>Potter, Hollis G.</creatorcontrib><creatorcontrib>Rodeo, Scott A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of sports medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakagawa, Yusuke</au><au>Fortier, Lisa A.</au><au>Mao, Jeremy J.</au><au>Lee, Chang Hun</au><au>Goodale, Margaret B.</au><au>Koff, Matthew F.</au><au>Uppstrom, Tyler J.</au><au>Croen, Brett</au><au>Wada, Susumu</au><au>Carballo, Camila B.</au><au>Potter, Hollis G.</au><au>Rodeo, Scott A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model</atitle><jtitle>The American journal of sports medicine</jtitle><addtitle>Am J Sports Med</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>47</volume><issue>11</issue><spage>2596</spage><epage>2607</epage><pages>2596-2607</pages><issn>0363-5465</issn><eissn>1552-3365</eissn><abstract>Background:
Artificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI).
Purpose:
To evaluate long-term outcome of meniscal replacement with growth factor–laden poly-ε-caprolactone (PCL) scaffolds.
Study Design:
Controlled laboratory study.
Methods:
Anatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups.
Results:
Remnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%).
Conclusion:
Previously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion.
Clinical Relevance:
A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menisci could be printed and available for off-the-shelf applications. Based on the 1-year duration of the study, the approach appears to be promising for meniscal regeneration in humans.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>31386550</pmid><doi>10.1177/0363546519865513</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Connective Tissue Growth Factor - metabolism Growth factors Histology Meniscus - surgery Models, Animal NMR Nuclear magnetic resonance Printing, Three-Dimensional - statistics & numerical data Sheep Sports medicine Tissue Scaffolds - statistics & numerical data Transforming Growth Factor beta3 - metabolism |
title | Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional–Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model |
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