A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis

In tissue engineering and regenerative medicine, the formation of vascular beds is an effective method to supply oxygen and nutrients to implanted cells or tissues to improve their survival and promote normal cellular functions. Various types of angiogenic materials have been developed by incorporat...

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Published in:RSC Advances
Main Authors: Mizuno, Yosuke, Taguchi, Tetsushi
Format: Text
Language:English
Published: The Royal Society of Chemistry 2020
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055140/
https://doi.org/10.1039/d0ra03593a
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spelling ftpubmed:oai:pubmedcentral.nih.gov:9055140 2023-05-15T13:09:24+02:00 A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis Mizuno, Yosuke Taguchi, Tetsushi 2020-06-30 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055140/ https://doi.org/10.1039/d0ra03593a en eng The Royal Society of Chemistry http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055140/ http://dx.doi.org/10.1039/d0ra03593a This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ CC-BY RSC Adv Chemistry Text 2020 ftpubmed https://doi.org/10.1039/d0ra03593a 2022-05-08T00:49:49Z In tissue engineering and regenerative medicine, the formation of vascular beds is an effective method to supply oxygen and nutrients to implanted cells or tissues to improve their survival and promote normal cellular functions. Various types of angiogenic materials have been developed by incorporating growth factors, such as vascular endothelial growth factor, in biocompatible materials. However, these exogenous growth factors suffer from instability and inactivation under physiological conditions. In this study, we designed a novel angiogenic electrospun fiber sheet (C16-FS) composed of Alaska pollock-derived gelatin (ApGltn) modified with hexadecyl (C16) groups to induce localized and sustained angiogenesis without growth factors. C16-FS was thermally crosslinked to enhance its stability. We demonstrated that C16-FS swells in phosphate-buffered saline for over 24 h and resists degradation. Laser doppler perfusion imaging showed that C16-FS induced increased blood perfusion when implanted subcutaneously in rats compared with unmodified ApGltn-fiber sheets (Org-FS) and the sham control. Furthermore, angiogenesis was sustained for up to 7 days following implantation. Immunohistochemical studies revealed elevated nuclear factor-κB and CD31 levels around the C16-FS implantation site compared with the Org-FS implantation site and the control incision site. These results demonstrate that C16-FS is a promising angiogenic material to promote the formation of vascular beds for cell and tissue transplantation without the need for growth factors. Text alaska pollock Alaska PubMed Central (PMC) RSC Advances 10 42 24800 24807
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Chemistry
spellingShingle Chemistry
Mizuno, Yosuke
Taguchi, Tetsushi
A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
topic_facet Chemistry
description In tissue engineering and regenerative medicine, the formation of vascular beds is an effective method to supply oxygen and nutrients to implanted cells or tissues to improve their survival and promote normal cellular functions. Various types of angiogenic materials have been developed by incorporating growth factors, such as vascular endothelial growth factor, in biocompatible materials. However, these exogenous growth factors suffer from instability and inactivation under physiological conditions. In this study, we designed a novel angiogenic electrospun fiber sheet (C16-FS) composed of Alaska pollock-derived gelatin (ApGltn) modified with hexadecyl (C16) groups to induce localized and sustained angiogenesis without growth factors. C16-FS was thermally crosslinked to enhance its stability. We demonstrated that C16-FS swells in phosphate-buffered saline for over 24 h and resists degradation. Laser doppler perfusion imaging showed that C16-FS induced increased blood perfusion when implanted subcutaneously in rats compared with unmodified ApGltn-fiber sheets (Org-FS) and the sham control. Furthermore, angiogenesis was sustained for up to 7 days following implantation. Immunohistochemical studies revealed elevated nuclear factor-κB and CD31 levels around the C16-FS implantation site compared with the Org-FS implantation site and the control incision site. These results demonstrate that C16-FS is a promising angiogenic material to promote the formation of vascular beds for cell and tissue transplantation without the need for growth factors.
format Text
author Mizuno, Yosuke
Taguchi, Tetsushi
author_facet Mizuno, Yosuke
Taguchi, Tetsushi
author_sort Mizuno, Yosuke
title A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
title_short A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
title_full A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
title_fullStr A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
title_full_unstemmed A hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
title_sort hydrophobic gelatin fiber sheet promotes secretion of endogenous vascular endothelial growth factor and stimulates angiogenesis
publisher The Royal Society of Chemistry
publishDate 2020
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055140/
https://doi.org/10.1039/d0ra03593a
genre alaska pollock
Alaska
genre_facet alaska pollock
Alaska
op_source RSC Adv
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055140/
http://dx.doi.org/10.1039/d0ra03593a
op_rights This journal is © The Royal Society of Chemistry
https://creativecommons.org/licenses/by/3.0/
op_rightsnorm CC-BY
op_doi https://doi.org/10.1039/d0ra03593a
container_title RSC Advances
container_volume 10
container_issue 42
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