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Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration

Rapid vascularization is required for the regeneration of dental pulp due to the spatially restricted tooth environment. Extracellular vesicles (EVs) released from mesenchymal stromal cells show potent proangiogenic effects. Since EVs suffer from rapid clearance and low accumulation in target tissue...

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Autores principales: Zhang, Siyuan, Thiebes, Anja Lena, Kreimendahl, Franziska, Ruetten, Stephan, Buhl, Eva Miriam, Wolf, Michael, Jockenhoevel, Stefan, Apel, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352754/
https://www.ncbi.nlm.nih.gov/pubmed/32545804
http://dx.doi.org/10.3390/ijms21124226
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author Zhang, Siyuan
Thiebes, Anja Lena
Kreimendahl, Franziska
Ruetten, Stephan
Buhl, Eva Miriam
Wolf, Michael
Jockenhoevel, Stefan
Apel, Christian
author_facet Zhang, Siyuan
Thiebes, Anja Lena
Kreimendahl, Franziska
Ruetten, Stephan
Buhl, Eva Miriam
Wolf, Michael
Jockenhoevel, Stefan
Apel, Christian
author_sort Zhang, Siyuan
collection PubMed
description Rapid vascularization is required for the regeneration of dental pulp due to the spatially restricted tooth environment. Extracellular vesicles (EVs) released from mesenchymal stromal cells show potent proangiogenic effects. Since EVs suffer from rapid clearance and low accumulation in target tissues, an injectable delivery system capable of maintaining a therapeutic dose of EVs over a longer period would be desirable. We fabricated an EV-fibrin gel composite as an in situ forming delivery system. EVs were isolated from dental pulp stem cells (DPSCs). Their effects on cell proliferation and migration were monitored in monolayers and hydrogels. Thereafter, endothelial cells and DPSCs were co-cultured in EV-fibrin gels and angiogenesis as well as collagen deposition were analyzed by two-photon laser microscopy. Our results showed that EVs enhanced cell growth and migration in 2D and 3D cultures. EV-fibrin gels facilitated vascular-like structure formation in less than seven days by increasing the release of VEGF. The EV-fibrin gel promoted the deposition of collagen I, III, and IV, and readily induced apoptosis during the initial stage of angiogenesis. In conclusion, we confirmed that EVs from DPSCs can promote angiogenesis in an injectable hydrogel in vitro, offering a novel and minimally invasive strategy for regenerative endodontic therapy.
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spelling pubmed-73527542020-07-15 Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration Zhang, Siyuan Thiebes, Anja Lena Kreimendahl, Franziska Ruetten, Stephan Buhl, Eva Miriam Wolf, Michael Jockenhoevel, Stefan Apel, Christian Int J Mol Sci Article Rapid vascularization is required for the regeneration of dental pulp due to the spatially restricted tooth environment. Extracellular vesicles (EVs) released from mesenchymal stromal cells show potent proangiogenic effects. Since EVs suffer from rapid clearance and low accumulation in target tissues, an injectable delivery system capable of maintaining a therapeutic dose of EVs over a longer period would be desirable. We fabricated an EV-fibrin gel composite as an in situ forming delivery system. EVs were isolated from dental pulp stem cells (DPSCs). Their effects on cell proliferation and migration were monitored in monolayers and hydrogels. Thereafter, endothelial cells and DPSCs were co-cultured in EV-fibrin gels and angiogenesis as well as collagen deposition were analyzed by two-photon laser microscopy. Our results showed that EVs enhanced cell growth and migration in 2D and 3D cultures. EV-fibrin gels facilitated vascular-like structure formation in less than seven days by increasing the release of VEGF. The EV-fibrin gel promoted the deposition of collagen I, III, and IV, and readily induced apoptosis during the initial stage of angiogenesis. In conclusion, we confirmed that EVs from DPSCs can promote angiogenesis in an injectable hydrogel in vitro, offering a novel and minimally invasive strategy for regenerative endodontic therapy. MDPI 2020-06-13 /pmc/articles/PMC7352754/ /pubmed/32545804 http://dx.doi.org/10.3390/ijms21124226 Text en © 2020 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
Zhang, Siyuan
Thiebes, Anja Lena
Kreimendahl, Franziska
Ruetten, Stephan
Buhl, Eva Miriam
Wolf, Michael
Jockenhoevel, Stefan
Apel, Christian
Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title_full Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title_fullStr Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title_full_unstemmed Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title_short Extracellular Vesicles-Loaded Fibrin Gel Supports Rapid Neovascularization for Dental Pulp Regeneration
title_sort extracellular vesicles-loaded fibrin gel supports rapid neovascularization for dental pulp regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352754/
https://www.ncbi.nlm.nih.gov/pubmed/32545804
http://dx.doi.org/10.3390/ijms21124226
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