Aligned nanofibers of decellularized muscle extracellular matrix for volumetric muscle loss
Volumetric muscle loss (VML) is a traumatic loss of muscle tissue that results in chronic functional impairment. When injured, skeletal muscle is capable of small‐scale repair; however, regenerative capacities are lost with VML due to a critical loss stem cells and extracellular matrix (ECM). Conseq...
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Veröffentlicht in: | Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2020-08, Vol.108 (6), p.2528-2537 |
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creator | Patel, Krishna H. Talovic, Muhamed Dunn, Andrew J. Patel, Anjali Vendrell, Sara Schwartz, Mark Garg, Koyal |
description | Volumetric muscle loss (VML) is a traumatic loss of muscle tissue that results in chronic functional impairment. When injured, skeletal muscle is capable of small‐scale repair; however, regenerative capacities are lost with VML due to a critical loss stem cells and extracellular matrix (ECM). Consequences of VML include either long‐term disability or delayed amputations of the affected limb. While the prevalence of VML is substantial, currently a successful clinical therapy has not been identified. In a previous study, an electrospun composed of polycaprolactone (PCL) and decellularized‐ECM (D‐ECM) supported satellite cell‐mediated myogenic activity in vitro. In this study, we investigate the extent to which this electrospun scaffold can support functional muscle regeneration in a murine model of VML. Experimental groups included no treatment, pure PCL treated, and PCL:D‐ECM (50:50 blend) treated VML defects. The PCL:D‐ECM scaffold treated VML muscles supported increased activity of anti‐inflammatory M2 macrophages (arginase+) at Day 28, compared to other experimental groups. Increased myofiber (MHC+) regeneration was observed histologically at both Days 7 and 28 post‐trauma in blend scaffold treated group compared to PCL treated and untreated groups. However, improvements in muscle weights and force production were not observed. Future studies would evaluate muscle function at longer time‐points post‐VML injury to allow sufficient time for reinnervation of regenerated muscle fibers. |
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When injured, skeletal muscle is capable of small‐scale repair; however, regenerative capacities are lost with VML due to a critical loss stem cells and extracellular matrix (ECM). Consequences of VML include either long‐term disability or delayed amputations of the affected limb. While the prevalence of VML is substantial, currently a successful clinical therapy has not been identified. In a previous study, an electrospun composed of polycaprolactone (PCL) and decellularized‐ECM (D‐ECM) supported satellite cell‐mediated myogenic activity in vitro. In this study, we investigate the extent to which this electrospun scaffold can support functional muscle regeneration in a murine model of VML. Experimental groups included no treatment, pure PCL treated, and PCL:D‐ECM (50:50 blend) treated VML defects. The PCL:D‐ECM scaffold treated VML muscles supported increased activity of anti‐inflammatory M2 macrophages (arginase+) at Day 28, compared to other experimental groups. Increased myofiber (MHC+) regeneration was observed histologically at both Days 7 and 28 post‐trauma in blend scaffold treated group compared to PCL treated and untreated groups. However, improvements in muscle weights and force production were not observed. Future studies would evaluate muscle function at longer time‐points post‐VML injury to allow sufficient time for reinnervation of regenerated muscle fibers.</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.34584</identifier><identifier>PMID: 32052931</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animal models ; Arginase ; Biomedical materials ; Electrospinning ; Extracellular matrix ; Inflammation ; Macrophages ; Materials research ; Materials science ; Muscles ; Nanofibers ; Polycaprolactone ; Regeneration ; Reinnervation ; Satellite cells ; Scaffolds ; Skeletal muscle ; Stem cell transplantation ; Stem cells ; Trauma</subject><ispartof>Journal of biomedical materials research. 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Part B, Applied biomaterials</title><addtitle>J Biomed Mater Res B Appl Biomater</addtitle><description>Volumetric muscle loss (VML) is a traumatic loss of muscle tissue that results in chronic functional impairment. When injured, skeletal muscle is capable of small‐scale repair; however, regenerative capacities are lost with VML due to a critical loss stem cells and extracellular matrix (ECM). Consequences of VML include either long‐term disability or delayed amputations of the affected limb. While the prevalence of VML is substantial, currently a successful clinical therapy has not been identified. In a previous study, an electrospun composed of polycaprolactone (PCL) and decellularized‐ECM (D‐ECM) supported satellite cell‐mediated myogenic activity in vitro. In this study, we investigate the extent to which this electrospun scaffold can support functional muscle regeneration in a murine model of VML. Experimental groups included no treatment, pure PCL treated, and PCL:D‐ECM (50:50 blend) treated VML defects. The PCL:D‐ECM scaffold treated VML muscles supported increased activity of anti‐inflammatory M2 macrophages (arginase+) at Day 28, compared to other experimental groups. Increased myofiber (MHC+) regeneration was observed histologically at both Days 7 and 28 post‐trauma in blend scaffold treated group compared to PCL treated and untreated groups. However, improvements in muscle weights and force production were not observed. Future studies would evaluate muscle function at longer time‐points post‐VML injury to allow sufficient time for reinnervation of regenerated muscle fibers.</description><subject>Animal models</subject><subject>Arginase</subject><subject>Biomedical materials</subject><subject>Electrospinning</subject><subject>Extracellular matrix</subject><subject>Inflammation</subject><subject>Macrophages</subject><subject>Materials research</subject><subject>Materials science</subject><subject>Muscles</subject><subject>Nanofibers</subject><subject>Polycaprolactone</subject><subject>Regeneration</subject><subject>Reinnervation</subject><subject>Satellite cells</subject><subject>Scaffolds</subject><subject>Skeletal muscle</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Trauma</subject><issn>1552-4973</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp90DtPwzAUBWALgaA8JnYUiQUJtfideKQVT4FYYGKwHOcapXKSYjdQ-PW4lDIwMNnW_XR0fRA6JHhEMKZn07IZlSPGRcE30IAIQYdcFWTz956zHbQb4zRhiQXbRjuMYkEVIwP0fO7rlxaqrDVt5-oSQsw6l1Vgwfvem1B_pmHTR-shg8U8mPUga8w81IvMdSF763zfQHraNfVdjPtoyxkf4eDn3ENPlxePk-vh3cPVzeT8bmiZyvlQOqu4ZdZZXimcSycMFMAJKFwUEnJhhGIVcVBSR8siDatcVVISKyvFsWV76GSVOwvdaw9xrps6Ltc0LXR91JQJnrNCEJbo8R867frQpu005UTRXEq1VKcrZUP6RgCnZ6FuTPjQBOtl5zp1rkv93XnSRz-ZfdlA9WvXJSdAV-C99vDxX5a-Hd-PV6lfhxCN1Q</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Patel, Krishna H.</creator><creator>Talovic, Muhamed</creator><creator>Dunn, Andrew J.</creator><creator>Patel, Anjali</creator><creator>Vendrell, Sara</creator><creator>Schwartz, Mark</creator><creator>Garg, Koyal</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</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>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202008</creationdate><title>Aligned nanofibers of decellularized muscle extracellular matrix for volumetric muscle loss</title><author>Patel, Krishna H. ; 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Part B, Applied biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patel, Krishna H.</au><au>Talovic, Muhamed</au><au>Dunn, Andrew J.</au><au>Patel, Anjali</au><au>Vendrell, Sara</au><au>Schwartz, Mark</au><au>Garg, Koyal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aligned nanofibers of decellularized muscle extracellular matrix for volumetric muscle loss</atitle><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle><addtitle>J Biomed Mater Res B Appl Biomater</addtitle><date>2020-08</date><risdate>2020</risdate><volume>108</volume><issue>6</issue><spage>2528</spage><epage>2537</epage><pages>2528-2537</pages><issn>1552-4973</issn><eissn>1552-4981</eissn><abstract>Volumetric muscle loss (VML) is a traumatic loss of muscle tissue that results in chronic functional impairment. When injured, skeletal muscle is capable of small‐scale repair; however, regenerative capacities are lost with VML due to a critical loss stem cells and extracellular matrix (ECM). Consequences of VML include either long‐term disability or delayed amputations of the affected limb. While the prevalence of VML is substantial, currently a successful clinical therapy has not been identified. In a previous study, an electrospun composed of polycaprolactone (PCL) and decellularized‐ECM (D‐ECM) supported satellite cell‐mediated myogenic activity in vitro. In this study, we investigate the extent to which this electrospun scaffold can support functional muscle regeneration in a murine model of VML. Experimental groups included no treatment, pure PCL treated, and PCL:D‐ECM (50:50 blend) treated VML defects. The PCL:D‐ECM scaffold treated VML muscles supported increased activity of anti‐inflammatory M2 macrophages (arginase+) at Day 28, compared to other experimental groups. Increased myofiber (MHC+) regeneration was observed histologically at both Days 7 and 28 post‐trauma in blend scaffold treated group compared to PCL treated and untreated groups. However, improvements in muscle weights and force production were not observed. Future studies would evaluate muscle function at longer time‐points post‐VML injury to allow sufficient time for reinnervation of regenerated muscle fibers.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32052931</pmid><doi>10.1002/jbm.b.34584</doi><tpages>10</tpages></addata></record> |
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subjects | Animal models Arginase Biomedical materials Electrospinning Extracellular matrix Inflammation Macrophages Materials research Materials science Muscles Nanofibers Polycaprolactone Regeneration Reinnervation Satellite cells Scaffolds Skeletal muscle Stem cell transplantation Stem cells Trauma |
title | Aligned nanofibers of decellularized muscle extracellular matrix for volumetric muscle loss |
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