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- PMID: 19260803
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Article: Decellularization of chondrocyte-encapsulated collagen microspheres: A three-dimensional model to study the effects of acellular matrix on stem cell fate
Title | Decellularization of chondrocyte-encapsulated collagen microspheres: A three-dimensional model to study the effects of acellular matrix on stem cell fate | ||||||||||||||
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Authors | |||||||||||||||
Issue Date | 2009 | ||||||||||||||
Publisher | Mary Ann Liebert, Inc. Publishers. The Journal's web site is located at http://www.liebertpub.com/publication.aspx?pub_id=261 | ||||||||||||||
Citation | Tissue Engineering - Part C: Methods, 2009, v. 15 n. 4, p. 697-706 How to Cite? | ||||||||||||||
Abstract | Extracellular matrix (ECM) partially constitutes the stem cell niche. Reconstituting the ECM niche in a three-dimensional (3D) configuration will significantly enhance our understanding of how stem cells interact with and respond to the ECM niche. In this study, we aimed to reconstitute a glycosaminoglycan (GAG)-rich ECM using a microencapsulation technology, produce acellular matrix using a decellularization technique, and investigate the effect of acellular matrix on stem cell fate by repopulating the matrix with human mesenchymal stem cells (hMSCs). We demonstrated that porcine chondrocytes were able to deposit a GAG-rich ECM within the 3D collagen microsphere. All decellularization treatment groups resulted in significant removal of chondrocyte nuclei, but acellular matrix was only achieved using 2% sodium deoxycholate. Nevertheless, decellularization resulted in significant loss in GAG content in almost all treatment groups, and the 2% sodium deoxycholate group was able to preserve about 40% of the GAGs compared with the control group. We further demonstrated that hMSCs seeded onto the decellularized microspheres were able to survive and penetrate into the centre, while hMSCs seeded in the acellular matrix showed positive immunostaining against sox9, indicating that they may be differentiating toward the chondrogenic lineage without the need to supplement the chondrogenic differentiation medium. © 2009 Mary Ann Liebert, Inc. | ||||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/68157 | ||||||||||||||
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.603 | ||||||||||||||
ISI Accession Number ID |
Funding Information: This work was supported by grants from AOSpine (AOSBRC-07-06); the Innovation and Technology Commission, the Hong Kong Government (GHP/050/06); the University Research Committee, the University of Hong Kong (10206799); and the Strategic Research Theme on Development, Growth and Reproduction. The authors thank Ms. Vicki Geall for editing the manuscript. | ||||||||||||||
References | |||||||||||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Cheng, HW | en_HK |
dc.contributor.author | Tsui, YK | en_HK |
dc.contributor.author | Cheung, KMC | en_HK |
dc.contributor.author | Chan, D | en_HK |
dc.contributor.author | Chan, BP | en_HK |
dc.date.accessioned | 2010-09-06T06:01:54Z | - |
dc.date.available | 2010-09-06T06:01:54Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Tissue Engineering - Part C: Methods, 2009, v. 15 n. 4, p. 697-706 | en_HK |
dc.identifier.issn | 1937-3384 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/68157 | - |
dc.description.abstract | Extracellular matrix (ECM) partially constitutes the stem cell niche. Reconstituting the ECM niche in a three-dimensional (3D) configuration will significantly enhance our understanding of how stem cells interact with and respond to the ECM niche. In this study, we aimed to reconstitute a glycosaminoglycan (GAG)-rich ECM using a microencapsulation technology, produce acellular matrix using a decellularization technique, and investigate the effect of acellular matrix on stem cell fate by repopulating the matrix with human mesenchymal stem cells (hMSCs). We demonstrated that porcine chondrocytes were able to deposit a GAG-rich ECM within the 3D collagen microsphere. All decellularization treatment groups resulted in significant removal of chondrocyte nuclei, but acellular matrix was only achieved using 2% sodium deoxycholate. Nevertheless, decellularization resulted in significant loss in GAG content in almost all treatment groups, and the 2% sodium deoxycholate group was able to preserve about 40% of the GAGs compared with the control group. We further demonstrated that hMSCs seeded onto the decellularized microspheres were able to survive and penetrate into the centre, while hMSCs seeded in the acellular matrix showed positive immunostaining against sox9, indicating that they may be differentiating toward the chondrogenic lineage without the need to supplement the chondrogenic differentiation medium. © 2009 Mary Ann Liebert, Inc. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Mary Ann Liebert, Inc. Publishers. The Journal's web site is located at http://www.liebertpub.com/publication.aspx?pub_id=261 | en_HK |
dc.relation.ispartof | Tissue Engineering - Part C: Methods | en_HK |
dc.rights | This is a copy of an article published in the Tissue Engineering. Part C. Methods © 2009 copyright Mary Ann Liebert, Inc.; Tissue Engineering. Part C. Methods is available online at: http://www.liebertonline.com. | - |
dc.subject.mesh | Cell Lineage - drug effects | - |
dc.subject.mesh | Chondrocytes - cytology - drug effects | - |
dc.subject.mesh | Collagen - pharmacology | - |
dc.subject.mesh | Extracellular Matrix - drug effects - metabolism | - |
dc.subject.mesh | Microspheres | - |
dc.title | Decellularization of chondrocyte-encapsulated collagen microspheres: A three-dimensional model to study the effects of acellular matrix on stem cell fate | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1937-3384&volume=15&issue=4&spage=697&epage=706&date=2009&atitle=Decellularization+of+chondrocyte-encapsulated+collagen+microspheres:+a+three-dimensional+model+to+study+the+effects+of+acellular+matrix+on+stem+cell+fate | en_HK |
dc.identifier.email | Cheung, KMC:cheungmc@hku.hk | en_HK |
dc.identifier.email | Chan, D:chand@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, BP:bpchan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Cheung, KMC=rp00387 | en_HK |
dc.identifier.authority | Chan, D=rp00540 | en_HK |
dc.identifier.authority | Chan, BP=rp00087 | en_HK |
dc.description.nature | published_or_final_version | en_US |
dc.identifier.doi | 10.1089/ten.tec.2008.0635 | en_HK |
dc.identifier.pmid | 19260803 | - |
dc.identifier.scopus | eid_2-s2.0-72249108768 | en_HK |
dc.identifier.hkuros | 169431 | en_HK |
dc.identifier.hkuros | 180120 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-72249108768&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 15 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 697 | en_HK |
dc.identifier.epage | 706 | en_HK |
dc.identifier.isi | WOS:000272609100017 | - |
dc.publisher.place | United States | en_HK |
dc.relation.project | Collagen biomaterial and bone marrow derived mesenchymal stem cell (MSCs) based therapy - Second generation tissue engineering solutions for cartilage repair | - |
dc.identifier.scopusauthorid | Cheng, HW=35794981100 | en_HK |
dc.identifier.scopusauthorid | Tsui, YK=7006760586 | en_HK |
dc.identifier.scopusauthorid | Cheung, KMC=7402406754 | en_HK |
dc.identifier.scopusauthorid | Chan, D=7402216545 | en_HK |
dc.identifier.scopusauthorid | Chan, BP=7201530390 | en_HK |
dc.identifier.issnl | 1937-3384 | - |