Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability
The present study aimed to prepare a kind of controlled-releasing insulin-like growth factor 1 (IGF-1)/spider silk protein nanofibrous membrane using a electrostatic spinning method and evaluated its effect on the cell viability of endothelial progenitor cells (EPCs). Recombinant spidroin named as G...
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Taylor & Francis Group
2021
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oai:doaj.org-article:887d833be3474f648b1506af236b5a572021-11-11T14:23:43ZPreparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability2165-59792165-598710.1080/21655979.2021.1982270https://doaj.org/article/887d833be3474f648b1506af236b5a572021-01-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1982270https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987The present study aimed to prepare a kind of controlled-releasing insulin-like growth factor 1 (IGF-1)/spider silk protein nanofibrous membrane using a electrostatic spinning method and evaluated its effect on the cell viability of endothelial progenitor cells (EPCs). Recombinant spidroin named as GMCDRSSP-IgF-1 was electro-spun into nanofibrous membrane which can be degraded by protease and be capable of sustained-release of IGF-1. The membrane can be degraded after being treated with thrombin. The release assay results showed that IGF-1 concentration could be maintained at 20 ng/ml for a long time with treatment of Tobacco Etch Virus (TEV) protease. The viability of EPCs on GMCDRSSP-IgF-1 nanofibrous membrane was significantly increased with the presence of TEV protease. The controlled and sustained release of IGF-1 from the nanofibrous membrane could promote the adhesion and viability of EPCs. In summary, the nanofibrous membrane that exhibits controlled degradation and sustained release of IGF-1 was prepared with electrostatic spinning from genetically modified recombinant spider silk protein. The nanofibrous membrane exhibited good blood compatibility and cytocompatibility. With the presence of TEV protease, the sustained-release of IGF-1 significantly promoted the adhesion and viability of EPCs. The new nanofibrous membrane can be potentially used as a scaffold for EPCs culture in vitro and future in vivo studies.Lifang ChenYulang HuangRongfeng YangJian XiaoJiajia GaoDebao ZhangDuanwen CaoXiao KeTaylor & Francis Grouparticlecontrolled-releasingnanofibrous membranedegradationigf-1endothelial progenitor cellstev proteaseBiotechnologyTP248.13-248.65ENBioengineered, Vol 12, Iss 1, Pp 8031-8042 (2021) |
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DOAJ |
language |
EN |
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controlled-releasing nanofibrous membrane degradation igf-1 endothelial progenitor cells tev protease Biotechnology TP248.13-248.65 |
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controlled-releasing nanofibrous membrane degradation igf-1 endothelial progenitor cells tev protease Biotechnology TP248.13-248.65 Lifang Chen Yulang Huang Rongfeng Yang Jian Xiao Jiajia Gao Debao Zhang Duanwen Cao Xiao Ke Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
description |
The present study aimed to prepare a kind of controlled-releasing insulin-like growth factor 1 (IGF-1)/spider silk protein nanofibrous membrane using a electrostatic spinning method and evaluated its effect on the cell viability of endothelial progenitor cells (EPCs). Recombinant spidroin named as GMCDRSSP-IgF-1 was electro-spun into nanofibrous membrane which can be degraded by protease and be capable of sustained-release of IGF-1. The membrane can be degraded after being treated with thrombin. The release assay results showed that IGF-1 concentration could be maintained at 20 ng/ml for a long time with treatment of Tobacco Etch Virus (TEV) protease. The viability of EPCs on GMCDRSSP-IgF-1 nanofibrous membrane was significantly increased with the presence of TEV protease. The controlled and sustained release of IGF-1 from the nanofibrous membrane could promote the adhesion and viability of EPCs. In summary, the nanofibrous membrane that exhibits controlled degradation and sustained release of IGF-1 was prepared with electrostatic spinning from genetically modified recombinant spider silk protein. The nanofibrous membrane exhibited good blood compatibility and cytocompatibility. With the presence of TEV protease, the sustained-release of IGF-1 significantly promoted the adhesion and viability of EPCs. The new nanofibrous membrane can be potentially used as a scaffold for EPCs culture in vitro and future in vivo studies. |
format |
article |
author |
Lifang Chen Yulang Huang Rongfeng Yang Jian Xiao Jiajia Gao Debao Zhang Duanwen Cao Xiao Ke |
author_facet |
Lifang Chen Yulang Huang Rongfeng Yang Jian Xiao Jiajia Gao Debao Zhang Duanwen Cao Xiao Ke |
author_sort |
Lifang Chen |
title |
Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
title_short |
Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
title_full |
Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
title_fullStr |
Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
title_full_unstemmed |
Preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
title_sort |
preparation of controlled degradation of insulin-like growth factor 1/spider silk protein nanofibrous membrane and its effect on endothelial progenitor cell viability |
publisher |
Taylor & Francis Group |
publishDate |
2021 |
url |
https://doaj.org/article/887d833be3474f648b1506af236b5a57 |
work_keys_str_mv |
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_version_ |
1718438955237507072 |