Sustained Release of BMP-2 in Bioprinted Alginate for Osteogenicity in Mice and Rats

The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the s...

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Published inPloS one Vol. 8; no. 8; p. e72610
Main Authors Poldervaart, Michelle T., Wang, Huanan, van der Stok, Johan, Weinans, Harrie, Leeuwenburgh, Sander C. G., Öner, F. Cumhur, Dhert, Wouter J. A., Alblas, Jacqueline
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 19.08.2013
Public Library of Science (PLoS)
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Abstract The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo.
AbstractList The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo.
The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo .
The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo.The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds offers many new possibilities regarding both biological and architectural properties of the scaffolds. This study investigates whether the sustained release of bone morphogenetic protein 2 (BMP-2) influences osteogenicity of tissue engineered bioprinted constructs. BMP-2 loaded on gelatin microparticles (GMPs) was used as a sustained release system, which was dispersed in hydrogel-based constructs and compared to direct inclusion of BMP-2 in alginate or control GMPs. The constructs were supplemented with goat multipotent stromal cells (gMSCs) and biphasic calcium phosphate to study osteogenic differentiation and bone formation respectively. BMP-2 release kinetics and bioactivity showed continuous release for three weeks coinciding with osteogenicity. Osteogenic differentiation and bone formation of bioprinted GMP containing constructs were investigated after subcutaneous implantation in mice or rats. BMP-2 significantly increased bone formation, which was not influenced by the release timing. We showed that 3D printing of controlled release particles is feasible and that the released BMP-2 directs osteogenic differentiation in vitro and in vivo.
Audience Academic
Author Weinans, Harrie
Dhert, Wouter J. A.
Alblas, Jacqueline
van der Stok, Johan
Öner, F. Cumhur
Leeuwenburgh, Sander C. G.
Wang, Huanan
Poldervaart, Michelle T.
AuthorAffiliation 4 Department of Biomechanical Engineering, Delft University of Technology, Delft, The Netherlands
5 Department of Rheumatology, University Medical Center Utrecht, Utrecht, The Netherlands
6 Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands
1 Department of Orthopaedics, University Medical Center Utrecht, Utrecht, The Netherlands
National University of Ireland, Galway, Ireland
3 Department of Orthopaedics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands
2 Department of Biomaterials, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands
AuthorAffiliation_xml – name: 1 Department of Orthopaedics, University Medical Center Utrecht, Utrecht, The Netherlands
– name: 5 Department of Rheumatology, University Medical Center Utrecht, Utrecht, The Netherlands
– name: 4 Department of Biomechanical Engineering, Delft University of Technology, Delft, The Netherlands
– name: 3 Department of Orthopaedics, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands
– name: 2 Department of Biomaterials, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands
– name: National University of Ireland, Galway, Ireland
– name: 6 Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands
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  givenname: Michelle T.
  surname: Poldervaart
  fullname: Poldervaart, Michelle T.
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  givenname: Huanan
  surname: Wang
  fullname: Wang, Huanan
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  givenname: Johan
  surname: van der Stok
  fullname: van der Stok, Johan
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  givenname: Sander C. G.
  surname: Leeuwenburgh
  fullname: Leeuwenburgh, Sander C. G.
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  givenname: F. Cumhur
  surname: Öner
  fullname: Öner, F. Cumhur
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  givenname: Wouter J. A.
  surname: Dhert
  fullname: Dhert, Wouter J. A.
– sequence: 8
  givenname: Jacqueline
  surname: Alblas
  fullname: Alblas, Jacqueline
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23977328$$D View this record in MEDLINE/PubMed
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Copyright COPYRIGHT 2013 Public Library of Science
2013 Poldervaart et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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DocumentTitleAlternate Prolonged BMP-2 Release in Bioprinted Scaffolds
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: MP SL H. Weinans FCO WD JA. Performed the experiments: MP H. Wang JvdS. Analyzed the data: MP H. Wang JvdS WD JA. Contributed reagents/materials/analysis tools: H. Wang SL H. Weinans. Wrote the paper: MP H. Wang JvdS H. Weinans SL FCO WD JA.
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20804200 - Biomacromolecules. 2010 Oct 11;11(10):2653-9
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Snippet The design of bioactive three-dimensional (3D) scaffolds is a major focus in bone tissue engineering. Incorporation of growth factors into bioprinted scaffolds...
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StartPage e72610
SubjectTerms 3D printing
Alginates - pharmacology
Alginic acid
Animals
Biocompatibility
Biodegradation
Biological activity
Biological properties
Biology
Biomechanics
Biomedical materials
Bioprinting - methods
Bone growth
Bone morphogenetic protein 2
Bone Morphogenetic Protein 2 - metabolism
Bone morphogenetic proteins
Calcium
Calcium phosphate
Calcium phosphates
Cell Differentiation - drug effects
Comparative analysis
Controlled release
Delayed-Action Preparations
Differentiation
Drug dosages
Engineering
Female
Fractures
Gelatin
Gelatin - pharmacology
Glucuronic Acid - pharmacology
Goats
Growth factors
Hexuronic Acids - pharmacology
Humans
Hydrogels
Hydroxyapatites - pharmacology
Implantation
Kinetics
Materials Science
Medicine
Mice, Nude
Microparticles
Microspheres
Multipotent Stem Cells - cytology
Multipotent Stem Cells - drug effects
Multipotent Stem Cells - metabolism
Osteocalcin - metabolism
Osteogenesis
Osteogenesis - drug effects
Phosphates
Polymers
Printing
Product introduction
Proteins
Rats
Rats, Wistar
Scaffolds
Stromal cells
Stromal Cells - cytology
Stromal Cells - drug effects
Stromal Cells - metabolism
Subcutaneous Tissue - metabolism
Surgical implants
Sustained release
Three dimensional printing
Tissue engineering
Tissue Scaffolds - chemistry
Vehicles
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Title Sustained Release of BMP-2 in Bioprinted Alginate for Osteogenicity in Mice and Rats
URI https://www.ncbi.nlm.nih.gov/pubmed/23977328
https://www.proquest.com/docview/1430786026
https://www.proquest.com/docview/1428269318
https://pubmed.ncbi.nlm.nih.gov/PMC3747086
https://doaj.org/article/5374cb3371b34e0fa69d34d8113fc621
http://dx.doi.org/10.1371/journal.pone.0072610
Volume 8
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