Cargando…
Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction
[Image: see text] Bone tissue engineering has emerged as an effective alternative treatment to the problem of bone defect. To repair a bone defect, antibiosis and osteogenesis are two essential aspects of the repair process. By searching the literature and performing exploratory experiments, we foun...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057706/ https://www.ncbi.nlm.nih.gov/pubmed/32149260 http://dx.doi.org/10.1021/acsomega.9b04249 |
_version_ | 1783503720117436416 |
---|---|
author | Peng, Yiyu Li, Lunhao Yuan, Qingyue Gu, Ping You, Zhengwei Zhuang, Ai Bi, Xiaoping |
author_facet | Peng, Yiyu Li, Lunhao Yuan, Qingyue Gu, Ping You, Zhengwei Zhuang, Ai Bi, Xiaoping |
author_sort | Peng, Yiyu |
collection | PubMed |
description | [Image: see text] Bone tissue engineering has emerged as an effective alternative treatment to the problem of bone defect. To repair a bone defect, antibiosis and osteogenesis are two essential aspects of the repair process. By searching the literature and performing exploratory experiments, we found that β defensin 2 (BD2), with bifunctional properties of antibiosis and osteogenesis, was a feasible alternative for traditional growth factors. The antimicrobial ability of BD2 against Staphylococcus aureus and Escherichia coli was studied by the spread plate and live/dead staining methods (low effective concentration of 20 ng/mL). BD2 was also demonstrated to enhance osteogenesis, with higher messenger RNA (mRNA) and protein expression of the osteogenic markers collagen I (Col1), runt-related transcription factor 2 (Runx2), osteopontin (Opn), and osteocalcin (Ocn) in vitro (1.5–2.5-fold increase compared with the control group in the most effective concentration group), which was consistent with the alkaline phosphatase (ALP) and alizarin red S (ARS) staining results. We implanted poly(sebacoyl diglyceride) (PSeD) combined with BD2 and rat bone tissue-derived mesenchymal stem cells (rBMSCs) under the back skin of rats and found that the inflammatory response was significantly lower with this combination than with the PSeD/rBMSCs scaffold without BD2 and the pure PSeD group and was similar to the control group. Importantly, when assessed in a critical-sized in vivo rat 8 m diameter calvaria defect model, a scaffold we developed combining bifunctional BD2 with porous organic polymer displayed an osteogenic effect that was 160–200% greater than the control group. The in vivo study results revealed a significant osteogenic response and antimicrobial effect and were consistent with the in vitro results. In summary, BD2 displayed a great potential of simultaneously promoting bone regeneration and preventing infection and could provide a viable alternative to traditional growth factors applied in bone defect repair. |
format | Online Article Text |
id | pubmed-7057706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70577062020-03-06 Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction Peng, Yiyu Li, Lunhao Yuan, Qingyue Gu, Ping You, Zhengwei Zhuang, Ai Bi, Xiaoping ACS Omega [Image: see text] Bone tissue engineering has emerged as an effective alternative treatment to the problem of bone defect. To repair a bone defect, antibiosis and osteogenesis are two essential aspects of the repair process. By searching the literature and performing exploratory experiments, we found that β defensin 2 (BD2), with bifunctional properties of antibiosis and osteogenesis, was a feasible alternative for traditional growth factors. The antimicrobial ability of BD2 against Staphylococcus aureus and Escherichia coli was studied by the spread plate and live/dead staining methods (low effective concentration of 20 ng/mL). BD2 was also demonstrated to enhance osteogenesis, with higher messenger RNA (mRNA) and protein expression of the osteogenic markers collagen I (Col1), runt-related transcription factor 2 (Runx2), osteopontin (Opn), and osteocalcin (Ocn) in vitro (1.5–2.5-fold increase compared with the control group in the most effective concentration group), which was consistent with the alkaline phosphatase (ALP) and alizarin red S (ARS) staining results. We implanted poly(sebacoyl diglyceride) (PSeD) combined with BD2 and rat bone tissue-derived mesenchymal stem cells (rBMSCs) under the back skin of rats and found that the inflammatory response was significantly lower with this combination than with the PSeD/rBMSCs scaffold without BD2 and the pure PSeD group and was similar to the control group. Importantly, when assessed in a critical-sized in vivo rat 8 m diameter calvaria defect model, a scaffold we developed combining bifunctional BD2 with porous organic polymer displayed an osteogenic effect that was 160–200% greater than the control group. The in vivo study results revealed a significant osteogenic response and antimicrobial effect and were consistent with the in vitro results. In summary, BD2 displayed a great potential of simultaneously promoting bone regeneration and preventing infection and could provide a viable alternative to traditional growth factors applied in bone defect repair. American Chemical Society 2020-02-18 /pmc/articles/PMC7057706/ /pubmed/32149260 http://dx.doi.org/10.1021/acsomega.9b04249 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Peng, Yiyu Li, Lunhao Yuan, Qingyue Gu, Ping You, Zhengwei Zhuang, Ai Bi, Xiaoping Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title | Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title_full | Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title_fullStr | Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title_full_unstemmed | Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title_short | Effect of Bifunctional β Defensin 2-Modified Scaffold on Bone Defect Reconstruction |
title_sort | effect of bifunctional β defensin 2-modified scaffold on bone defect reconstruction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057706/ https://www.ncbi.nlm.nih.gov/pubmed/32149260 http://dx.doi.org/10.1021/acsomega.9b04249 |
work_keys_str_mv | AT pengyiyu effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT lilunhao effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT yuanqingyue effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT guping effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT youzhengwei effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT zhuangai effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction AT bixiaoping effectofbifunctionalbdefensin2modifiedscaffoldonbonedefectreconstruction |