Cargando…
A Customized Self-Assembling Peptide Hydrogel-Wrapped Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like Structures
[Image: see text] Pulp regeneration is to replace the inflamed/necrotic pulp tissue with regenerated pulp-like tissue to rejuvenate the teeth. Self-assembling peptide hydrogels RADA16-I (Ac-(RADA16-I)(4)-CONH(2)) can provide a three-dimensional environment for cells. The stem cell factor (SCF) plays...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364552/ https://www.ncbi.nlm.nih.gov/pubmed/32685822 http://dx.doi.org/10.1021/acsomega.0c01266 |
_version_ | 1783559852525617152 |
---|---|
author | Mu, Xiaodan Shi, Lei Pan, Shuang He, Lina Niu, Yumei Wang, Xiumei |
author_facet | Mu, Xiaodan Shi, Lei Pan, Shuang He, Lina Niu, Yumei Wang, Xiumei |
author_sort | Mu, Xiaodan |
collection | PubMed |
description | [Image: see text] Pulp regeneration is to replace the inflamed/necrotic pulp tissue with regenerated pulp-like tissue to rejuvenate the teeth. Self-assembling peptide hydrogels RADA16-I (Ac-(RADA16-I)(4)-CONH(2)) can provide a three-dimensional environment for cells. The stem cell factor (SCF) plays a crucial role in homing stem cells. Combining these advantages, our study investigated the effects of SCF-RADA16-I on adhesion, proliferation, and migration of human dental pulp stem cells (DPSCs) and the angiogenesis of human umbilical vein endothelial cells (HUVECs). The β-sheet and grid structure were observed by circular dichroism (CD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Cytoskeleton staining, living cell staining, cell viability, cell migration, angiogenesis, and western blot assays were performed, and the results indicated that all the SCF groups were superior to the corresponding non-SCF groups in cell adhesion, proliferation, migration, and angiogenesis. RADA16-I provided a three-dimensional environment for DPSCs. Besides, the SCF promoted HUVECs to form more vascular-like structures and release more vascular endothelial growth factor A. In summary, the SCF-loaded RADA16-I scaffold improved adhesion, proliferation, and migration of DPSCs and the formation of more vascular-like structures of HUVECs. SCF-RADA16-I holds promise for guided pulp regeneration, and it can potentially be applied widely in tissue engineering and translational medicine in the future. |
format | Online Article Text |
id | pubmed-7364552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-73645522020-07-17 A Customized Self-Assembling Peptide Hydrogel-Wrapped Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like Structures Mu, Xiaodan Shi, Lei Pan, Shuang He, Lina Niu, Yumei Wang, Xiumei ACS Omega [Image: see text] Pulp regeneration is to replace the inflamed/necrotic pulp tissue with regenerated pulp-like tissue to rejuvenate the teeth. Self-assembling peptide hydrogels RADA16-I (Ac-(RADA16-I)(4)-CONH(2)) can provide a three-dimensional environment for cells. The stem cell factor (SCF) plays a crucial role in homing stem cells. Combining these advantages, our study investigated the effects of SCF-RADA16-I on adhesion, proliferation, and migration of human dental pulp stem cells (DPSCs) and the angiogenesis of human umbilical vein endothelial cells (HUVECs). The β-sheet and grid structure were observed by circular dichroism (CD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). Cytoskeleton staining, living cell staining, cell viability, cell migration, angiogenesis, and western blot assays were performed, and the results indicated that all the SCF groups were superior to the corresponding non-SCF groups in cell adhesion, proliferation, migration, and angiogenesis. RADA16-I provided a three-dimensional environment for DPSCs. Besides, the SCF promoted HUVECs to form more vascular-like structures and release more vascular endothelial growth factor A. In summary, the SCF-loaded RADA16-I scaffold improved adhesion, proliferation, and migration of DPSCs and the formation of more vascular-like structures of HUVECs. SCF-RADA16-I holds promise for guided pulp regeneration, and it can potentially be applied widely in tissue engineering and translational medicine in the future. American Chemical Society 2020-06-28 /pmc/articles/PMC7364552/ /pubmed/32685822 http://dx.doi.org/10.1021/acsomega.0c01266 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Mu, Xiaodan Shi, Lei Pan, Shuang He, Lina Niu, Yumei Wang, Xiumei A Customized Self-Assembling Peptide Hydrogel-Wrapped Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like Structures |
title | A Customized Self-Assembling Peptide Hydrogel-Wrapped
Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like
Structures |
title_full | A Customized Self-Assembling Peptide Hydrogel-Wrapped
Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like
Structures |
title_fullStr | A Customized Self-Assembling Peptide Hydrogel-Wrapped
Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like
Structures |
title_full_unstemmed | A Customized Self-Assembling Peptide Hydrogel-Wrapped
Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like
Structures |
title_short | A Customized Self-Assembling Peptide Hydrogel-Wrapped
Stem Cell Factor Targeting Pulp Regeneration Rich in Vascular-Like
Structures |
title_sort | customized self-assembling peptide hydrogel-wrapped
stem cell factor targeting pulp regeneration rich in vascular-like
structures |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364552/ https://www.ncbi.nlm.nih.gov/pubmed/32685822 http://dx.doi.org/10.1021/acsomega.0c01266 |
work_keys_str_mv | AT muxiaodan acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT shilei acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT panshuang acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT helina acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT niuyumei acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT wangxiumei acustomizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT muxiaodan customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT shilei customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT panshuang customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT helina customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT niuyumei customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures AT wangxiumei customizedselfassemblingpeptidehydrogelwrappedstemcellfactortargetingpulpregenerationrichinvascularlikestructures |