Electrospun cartilage-derived matrix scaffolds for cartilage tissue engineering

Macroscale scaffolds created from cartilage‐derived matrix (CDM) demonstrate chondroinductive or chondro‐inductive properties, but many fabrication methods do not allow for control of nanoscale architecture. In this regard, electrospun scaffolds have shown significant promise for cartilage tissue en...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2014-11, Vol.102 (11), p.3998-4008
Hauptverfasser: Garrigues, N. William, Little, Dianne, Sanchez-Adams, Johannah, Ruch, David S., Guilak, Farshid
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container_end_page 4008
container_issue 11
container_start_page 3998
container_title Journal of biomedical materials research. Part A
container_volume 102
creator Garrigues, N. William
Little, Dianne
Sanchez-Adams, Johannah
Ruch, David S.
Guilak, Farshid
description Macroscale scaffolds created from cartilage‐derived matrix (CDM) demonstrate chondroinductive or chondro‐inductive properties, but many fabrication methods do not allow for control of nanoscale architecture. In this regard, electrospun scaffolds have shown significant promise for cartilage tissue engineering. However, nanofibrous materials generally exhibit a relatively small pore size and require techniques such as multilayering or the inclusion of sacrificial fibers to enhance cellular infiltration. The objectives of this study were (1) to compare multilayer to single‐layer electrospun poly(ɛ‐caprolactone) (PCL) scaffolds for cartilage tissue engineering, and (2) to determine whether incorporation of CDM into the PCL fibers would enhance chondrogenesis by human adipose‐derived stem cells (hASCs). PCL and PCL–CDM scaffolds were prepared by sequential collection of 60 electrospun layers from the surface of a grounded saline bath into a single scaffold, or by continuous electrospinning onto the surface of a grounded saline bath and harvest as a single‐layer scaffold. Scaffolds were seeded with hASCs and evaluated over 28 days in culture. The predominant effects on hASCs of incorporation of CDM into scaffolds were to stimulate sulfated glycosaminoglycan synthesis and COL10A1 gene expression. Compared with single‐layer scaffolds, multilayer scaffolds enhanced cell infiltration and ACAN gene expression. However, compared with single‐layer constructs, multilayer PCL constructs had a much lower elastic modulus, and PCL–CDM constructs had an elastic modulus approximately 1% that of PCL constructs. These data suggest that multilayer electrospun constructs enhance homogeneous cell seeding, and that the inclusion of CDM stimulates chondrogenesis‐related bioactivity. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 3998–4008, 2014.
doi_str_mv 10.1002/jbm.a.35068
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William</creatorcontrib><creatorcontrib>Little, Dianne</creatorcontrib><creatorcontrib>Sanchez-Adams, Johannah</creatorcontrib><creatorcontrib>Ruch, David S.</creatorcontrib><creatorcontrib>Guilak, Farshid</creatorcontrib><title>Electrospun cartilage-derived matrix scaffolds for cartilage tissue engineering</title><title>Journal of biomedical materials research. Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Macroscale scaffolds created from cartilage‐derived matrix (CDM) demonstrate chondroinductive or chondro‐inductive properties, but many fabrication methods do not allow for control of nanoscale architecture. In this regard, electrospun scaffolds have shown significant promise for cartilage tissue engineering. However, nanofibrous materials generally exhibit a relatively small pore size and require techniques such as multilayering or the inclusion of sacrificial fibers to enhance cellular infiltration. The objectives of this study were (1) to compare multilayer to single‐layer electrospun poly(ɛ‐caprolactone) (PCL) scaffolds for cartilage tissue engineering, and (2) to determine whether incorporation of CDM into the PCL fibers would enhance chondrogenesis by human adipose‐derived stem cells (hASCs). PCL and PCL–CDM scaffolds were prepared by sequential collection of 60 electrospun layers from the surface of a grounded saline bath into a single scaffold, or by continuous electrospinning onto the surface of a grounded saline bath and harvest as a single‐layer scaffold. Scaffolds were seeded with hASCs and evaluated over 28 days in culture. The predominant effects on hASCs of incorporation of CDM into scaffolds were to stimulate sulfated glycosaminoglycan synthesis and COL10A1 gene expression. Compared with single‐layer scaffolds, multilayer scaffolds enhanced cell infiltration and ACAN gene expression. 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J Biomed Mater Res Part A: 102A: 3998–4008, 2014.</description><subject>Adipose Tissue - cytology</subject><subject>Adipose Tissue - metabolism</subject><subject>Adult</subject><subject>Aggrecans - biosynthesis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cartilage</subject><subject>Cartilage - chemistry</subject><subject>Cartilage - cytology</subject><subject>Cartilage - metabolism</subject><subject>Cells, Cultured</subject><subject>chondrogenesis</subject><subject>Collagen Type XI - biosynthesis</subject><subject>Construction</subject><subject>Controllers</subject><subject>Diseases of the osteoarticular system</subject><subject>Elastic Modulus</subject><subject>Electrospinning</subject><subject>electrospun</subject><subject>extracellular matrix</subject><subject>Extracellular Matrix - chemistry</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. 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William</creator><creator>Little, Dianne</creator><creator>Sanchez-Adams, Johannah</creator><creator>Ruch, David S.</creator><creator>Guilak, Farshid</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</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>5PM</scope></search><sort><creationdate>201411</creationdate><title>Electrospun cartilage-derived matrix scaffolds for cartilage tissue engineering</title><author>Garrigues, N. 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In this regard, electrospun scaffolds have shown significant promise for cartilage tissue engineering. However, nanofibrous materials generally exhibit a relatively small pore size and require techniques such as multilayering or the inclusion of sacrificial fibers to enhance cellular infiltration. The objectives of this study were (1) to compare multilayer to single‐layer electrospun poly(ɛ‐caprolactone) (PCL) scaffolds for cartilage tissue engineering, and (2) to determine whether incorporation of CDM into the PCL fibers would enhance chondrogenesis by human adipose‐derived stem cells (hASCs). PCL and PCL–CDM scaffolds were prepared by sequential collection of 60 electrospun layers from the surface of a grounded saline bath into a single scaffold, or by continuous electrospinning onto the surface of a grounded saline bath and harvest as a single‐layer scaffold. Scaffolds were seeded with hASCs and evaluated over 28 days in culture. The predominant effects on hASCs of incorporation of CDM into scaffolds were to stimulate sulfated glycosaminoglycan synthesis and COL10A1 gene expression. Compared with single‐layer scaffolds, multilayer scaffolds enhanced cell infiltration and ACAN gene expression. However, compared with single‐layer constructs, multilayer PCL constructs had a much lower elastic modulus, and PCL–CDM constructs had an elastic modulus approximately 1% that of PCL constructs. These data suggest that multilayer electrospun constructs enhance homogeneous cell seeding, and that the inclusion of CDM stimulates chondrogenesis‐related bioactivity. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 3998–4008, 2014.</abstract><cop>Hoboken, NJ</cop><pub>Blackwell Publishing Ltd</pub><pmid>24375991</pmid><doi>10.1002/jbm.a.35068</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Adipose Tissue - cytology
Adipose Tissue - metabolism
Adult
Aggrecans - biosynthesis
Animals
Biological and medical sciences
Biotechnology
Cartilage
Cartilage - chemistry
Cartilage - cytology
Cartilage - metabolism
Cells, Cultured
chondrogenesis
Collagen Type XI - biosynthesis
Construction
Controllers
Diseases of the osteoarticular system
Elastic Modulus
Electrospinning
electrospun
extracellular matrix
Extracellular Matrix - chemistry
Female
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation
Glycosaminoglycans - biosynthesis
Health. Pharmaceutical industry
Humans
Industrial applications and implications. Economical aspects
Medical sciences
mesenchymal stem cell
Middle Aged
Miscellaneous
Multilayers
nanofiber
Nanofibers - chemistry
Nanostructure
Osteoarthritis
Polyesters - chemistry
Porosity
Programmable logic devices
Scaffolds
Stem Cells - cytology
Stem Cells - metabolism
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Swine
Technology. Biomaterials. Equipments
Tissue engineering
Tissue Engineering - methods
Tissue Scaffolds - chemistry
title Electrospun cartilage-derived matrix scaffolds for cartilage tissue engineering
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