Cargando…

Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells

Multilayer composite membrane of biomaterials can increase the function of adipose stem cells or osteoprogenitor cells. Recent evidence indicates endothelial progenitor cells (EPCs) and EPCs released microvesicles (MVs) play important roles in angiogenesis and vascular repair. Here, we investigated...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Bingyan, Pan, Qunwen, Li, Zhanghua, Zhao, Mingyan, Liao, Xiaorong, Wu, Keng, Ma, Xiaotang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846769/
https://www.ncbi.nlm.nih.gov/pubmed/27190523
http://dx.doi.org/10.1155/2016/4796578
_version_ 1782429099223941120
author Dai, Bingyan
Pan, Qunwen
Li, Zhanghua
Zhao, Mingyan
Liao, Xiaorong
Wu, Keng
Ma, Xiaotang
author_facet Dai, Bingyan
Pan, Qunwen
Li, Zhanghua
Zhao, Mingyan
Liao, Xiaorong
Wu, Keng
Ma, Xiaotang
author_sort Dai, Bingyan
collection PubMed
description Multilayer composite membrane of biomaterials can increase the function of adipose stem cells or osteoprogenitor cells. Recent evidence indicates endothelial progenitor cells (EPCs) and EPCs released microvesicles (MVs) play important roles in angiogenesis and vascular repair. Here, we investigated the effects of biomaterial multilayer membranes of hyaluronic acid (HA) or chondroitin sulfate (CS) and Collagen I (Col I) on the functions and MVs release of EPCs. Layer-by-layer (LBL) technology was applied to construct the multilayer composite membranes. Four types of the membranes constructed by adsorbing either HA or CS and Col I alternatively with different top layers were studied. The results showed that all four types of multilayer composite membranes could promote EPCs proliferation and migration and inhibit cell senility, apoptosis, and the expression of activated caspase-3. Interestingly, these biomaterials increased the release and the miR-126 level of EPCs-MVs. Moreover, the CS-Col I membrane with CS on the top layer showed the most effects on promoting EPCs proliferation, EPCs-MV release, and miR-126 level in EPCs-MVs. In conclusion, HA/CS and Collagen I composed multilayer composite membranes can promote EPCs functions and release of miR-126 riched EPCs-MVs, which provides a novel strategy for tissue repair treatment.
format Online
Article
Text
id pubmed-4846769
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-48467692016-05-17 Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells Dai, Bingyan Pan, Qunwen Li, Zhanghua Zhao, Mingyan Liao, Xiaorong Wu, Keng Ma, Xiaotang Stem Cells Int Research Article Multilayer composite membrane of biomaterials can increase the function of adipose stem cells or osteoprogenitor cells. Recent evidence indicates endothelial progenitor cells (EPCs) and EPCs released microvesicles (MVs) play important roles in angiogenesis and vascular repair. Here, we investigated the effects of biomaterial multilayer membranes of hyaluronic acid (HA) or chondroitin sulfate (CS) and Collagen I (Col I) on the functions and MVs release of EPCs. Layer-by-layer (LBL) technology was applied to construct the multilayer composite membranes. Four types of the membranes constructed by adsorbing either HA or CS and Col I alternatively with different top layers were studied. The results showed that all four types of multilayer composite membranes could promote EPCs proliferation and migration and inhibit cell senility, apoptosis, and the expression of activated caspase-3. Interestingly, these biomaterials increased the release and the miR-126 level of EPCs-MVs. Moreover, the CS-Col I membrane with CS on the top layer showed the most effects on promoting EPCs proliferation, EPCs-MV release, and miR-126 level in EPCs-MVs. In conclusion, HA/CS and Collagen I composed multilayer composite membranes can promote EPCs functions and release of miR-126 riched EPCs-MVs, which provides a novel strategy for tissue repair treatment. Hindawi Publishing Corporation 2016 2016-04-13 /pmc/articles/PMC4846769/ /pubmed/27190523 http://dx.doi.org/10.1155/2016/4796578 Text en Copyright © 2016 Bingyan Dai et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dai, Bingyan
Pan, Qunwen
Li, Zhanghua
Zhao, Mingyan
Liao, Xiaorong
Wu, Keng
Ma, Xiaotang
Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title_full Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title_fullStr Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title_full_unstemmed Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title_short Multilayer Membranes of Glycosaminoglycans and Collagen I Biomaterials Modulate the Function and Microvesicle Release of Endothelial Progenitor Cells
title_sort multilayer membranes of glycosaminoglycans and collagen i biomaterials modulate the function and microvesicle release of endothelial progenitor cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846769/
https://www.ncbi.nlm.nih.gov/pubmed/27190523
http://dx.doi.org/10.1155/2016/4796578
work_keys_str_mv AT daibingyan multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT panqunwen multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT lizhanghua multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT zhaomingyan multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT liaoxiaorong multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT wukeng multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells
AT maxiaotang multilayermembranesofglycosaminoglycansandcollagenibiomaterialsmodulatethefunctionandmicrovesiclereleaseofendothelialprogenitorcells