Cargando…

Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro

Introduction: Resorbable synthetic scaffolds are promising for different indications, especially in the context of bone regeneration. However, they require additional biological components to enhance their osteogenic potential. In addition to different cell types, autologous blood-derived matrices o...

Descripción completa

Detalles Bibliográficos
Autores principales: Al-Maawi, Sarah, Dohle, Eva, Lim, Jing, Weigl, Paul, Teoh, Swee Hin, Sader, Robert, Ghanaati, Shahram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926906/
https://www.ncbi.nlm.nih.gov/pubmed/33671550
http://dx.doi.org/10.3390/ijms22042159
_version_ 1783659570109874176
author Al-Maawi, Sarah
Dohle, Eva
Lim, Jing
Weigl, Paul
Teoh, Swee Hin
Sader, Robert
Ghanaati, Shahram
author_facet Al-Maawi, Sarah
Dohle, Eva
Lim, Jing
Weigl, Paul
Teoh, Swee Hin
Sader, Robert
Ghanaati, Shahram
author_sort Al-Maawi, Sarah
collection PubMed
description Introduction: Resorbable synthetic scaffolds are promising for different indications, especially in the context of bone regeneration. However, they require additional biological components to enhance their osteogenic potential. In addition to different cell types, autologous blood-derived matrices offer many advantages to enhance the regenerative capacity of biomaterials. The present study aimed to analyze whether biologization of a PCL-mesh coated using differently centrifuged Platelet rich fibrin (PRF) matrices will have a positive influence on primary human osteoblasts activity in vitro. A polymeric resorbable scaffold (Osteomesh, Osteopore(TM) (OP), Singapore) was combined with differently centrifuged PRF matrices to evaluate the additional influence of this biologization concept on bone regeneration in vitro. Peripheral blood of three healthy donors was used to gain PRF matrices centrifuged either at High (710× g, 8 min) or Low (44× g, 8 min) relative centrifugal force (RCF) according to the low speed centrifugation concept (LSCC). OP-PRF constructs were cultured with pOBs. POBs cultured on the uncoated OP served as a control. After three and seven days of cultivation, cell culture supernatants were collected to analyze the pOBs activity by determining the concentrations of VEGF, TGF-β1, PDGF, OPG, IL-8, and ALP- activity. Immunofluorescence staining was used to evaluate the Osteopontin expression of pOBs. After three days, the group of OP+PRF(Low)+pOBs showed significantly higher expression of IL-8, TGF-ß1, PDGF, and VEGF compared to the group of OP+PRF(High)+pOBs and OP+pOBs. Similar results were observed on day 7. Moreover, OP+PRF(Low)+pOBs exhibited significantly higher activity of ALP compared to OP+PRF(High)+pOBs and OP+pOBs. Immunofluorescence staining showed a higher number of pOBs adherent to OP+PRF(Low)+pOBs compared to the groups OP+PRF(High)+pOBs and OP+pOBs. To the best of our knowledge, this study is the first to investigate the osteoblasts activity when cultured on a PRF-coated PCL-mesh in vitro. The presented results suggest that PRF(Low) centrifuged according to LSCC exhibits autologous blood cells and growth factors, seem to have a significant effect on osteogenesis. Thereby, the combination of OP with PRF(Low) showed promising results to support bone regeneration. Further in vivo studies are required to verify the results and carry out potential results for clinical translation.
format Online
Article
Text
id pubmed-7926906
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79269062021-03-04 Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro Al-Maawi, Sarah Dohle, Eva Lim, Jing Weigl, Paul Teoh, Swee Hin Sader, Robert Ghanaati, Shahram Int J Mol Sci Article Introduction: Resorbable synthetic scaffolds are promising for different indications, especially in the context of bone regeneration. However, they require additional biological components to enhance their osteogenic potential. In addition to different cell types, autologous blood-derived matrices offer many advantages to enhance the regenerative capacity of biomaterials. The present study aimed to analyze whether biologization of a PCL-mesh coated using differently centrifuged Platelet rich fibrin (PRF) matrices will have a positive influence on primary human osteoblasts activity in vitro. A polymeric resorbable scaffold (Osteomesh, Osteopore(TM) (OP), Singapore) was combined with differently centrifuged PRF matrices to evaluate the additional influence of this biologization concept on bone regeneration in vitro. Peripheral blood of three healthy donors was used to gain PRF matrices centrifuged either at High (710× g, 8 min) or Low (44× g, 8 min) relative centrifugal force (RCF) according to the low speed centrifugation concept (LSCC). OP-PRF constructs were cultured with pOBs. POBs cultured on the uncoated OP served as a control. After three and seven days of cultivation, cell culture supernatants were collected to analyze the pOBs activity by determining the concentrations of VEGF, TGF-β1, PDGF, OPG, IL-8, and ALP- activity. Immunofluorescence staining was used to evaluate the Osteopontin expression of pOBs. After three days, the group of OP+PRF(Low)+pOBs showed significantly higher expression of IL-8, TGF-ß1, PDGF, and VEGF compared to the group of OP+PRF(High)+pOBs and OP+pOBs. Similar results were observed on day 7. Moreover, OP+PRF(Low)+pOBs exhibited significantly higher activity of ALP compared to OP+PRF(High)+pOBs and OP+pOBs. Immunofluorescence staining showed a higher number of pOBs adherent to OP+PRF(Low)+pOBs compared to the groups OP+PRF(High)+pOBs and OP+pOBs. To the best of our knowledge, this study is the first to investigate the osteoblasts activity when cultured on a PRF-coated PCL-mesh in vitro. The presented results suggest that PRF(Low) centrifuged according to LSCC exhibits autologous blood cells and growth factors, seem to have a significant effect on osteogenesis. Thereby, the combination of OP with PRF(Low) showed promising results to support bone regeneration. Further in vivo studies are required to verify the results and carry out potential results for clinical translation. MDPI 2021-02-22 /pmc/articles/PMC7926906/ /pubmed/33671550 http://dx.doi.org/10.3390/ijms22042159 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Al-Maawi, Sarah
Dohle, Eva
Lim, Jing
Weigl, Paul
Teoh, Swee Hin
Sader, Robert
Ghanaati, Shahram
Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title_full Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title_fullStr Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title_full_unstemmed Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title_short Biologization of Pcl-Mesh Using Platelet Rich Fibrin (Prf) Enhances Its Regenerative Potential In Vitro
title_sort biologization of pcl-mesh using platelet rich fibrin (prf) enhances its regenerative potential in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926906/
https://www.ncbi.nlm.nih.gov/pubmed/33671550
http://dx.doi.org/10.3390/ijms22042159
work_keys_str_mv AT almaawisarah biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT dohleeva biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT limjing biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT weiglpaul biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT teohsweehin biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT saderrobert biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro
AT ghanaatishahram biologizationofpclmeshusingplateletrichfibrinprfenhancesitsregenerativepotentialinvitro