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Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering

Angiogenesis is a vital step in tissue regeneration. Hence, the current study aimed to prepare oxidized dextran (Odex)/collagen (Col)‐hydrogels with laminin (LMN), as an angiogenic extracellular matrix (ECM) component, for promoting human umbilical vein endothelial cell (HUVEC) proliferation and fun...

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Autores principales: Sarvestani, Fatemeh Sabet, Tamaddon, Ali‐Mohammad, Yaghoobi, Ramin, Geramizadeh, Bita, Azarpira, Negar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317976/
https://www.ncbi.nlm.nih.gov/pubmed/37408870
http://dx.doi.org/10.1002/elsc.202200140
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author Sarvestani, Fatemeh Sabet
Tamaddon, Ali‐Mohammad
Yaghoobi, Ramin
Geramizadeh, Bita
Azarpira, Negar
author_facet Sarvestani, Fatemeh Sabet
Tamaddon, Ali‐Mohammad
Yaghoobi, Ramin
Geramizadeh, Bita
Azarpira, Negar
author_sort Sarvestani, Fatemeh Sabet
collection PubMed
description Angiogenesis is a vital step in tissue regeneration. Hence, the current study aimed to prepare oxidized dextran (Odex)/collagen (Col)‐hydrogels with laminin (LMN), as an angiogenic extracellular matrix (ECM) component, for promoting human umbilical vein endothelial cell (HUVEC) proliferation and function. Odex/Col scaffolds were constructed at various concentrations and temperatures. Using oscillatory rheometry, scanning electron microscopy (SEM), and cell viability testing, the scaffolds were characterized, and then HUVEC proliferation and function was compared with or without LMN. The gelation time could be modified by altering the Odex/Col mass ratio as well as the temperature. SEM showed that Odex/Col hydrogels had a more regular three‐dimensional (3D) porous structure than the Col hydrogels. Moreover, HUVECs grew faster in the Col scaffold (12 mg/mL), whereas the Odex (30 mg/mL)/Col (6 mg/mL) scaffold exhibited the lowest apoptosis index. Furthermore, the expression level of vascular endothelial growth factor (VEGF) mRNA in the group without LMN was higher than that with LMN, and the Odex (30 mg/mL)/Col (6 mg/mL) scaffold without LMN had the highest VEGF protein secretion, allowing the cells to survive and function effectively. Odex/Col scaffolds, with or without LMN, are proposed as a tissue engineering construct to improve HUVEC survival and function for angiogenesis.
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spelling pubmed-103179762023-07-05 Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering Sarvestani, Fatemeh Sabet Tamaddon, Ali‐Mohammad Yaghoobi, Ramin Geramizadeh, Bita Azarpira, Negar Eng Life Sci Research Articles Angiogenesis is a vital step in tissue regeneration. Hence, the current study aimed to prepare oxidized dextran (Odex)/collagen (Col)‐hydrogels with laminin (LMN), as an angiogenic extracellular matrix (ECM) component, for promoting human umbilical vein endothelial cell (HUVEC) proliferation and function. Odex/Col scaffolds were constructed at various concentrations and temperatures. Using oscillatory rheometry, scanning electron microscopy (SEM), and cell viability testing, the scaffolds were characterized, and then HUVEC proliferation and function was compared with or without LMN. The gelation time could be modified by altering the Odex/Col mass ratio as well as the temperature. SEM showed that Odex/Col hydrogels had a more regular three‐dimensional (3D) porous structure than the Col hydrogels. Moreover, HUVECs grew faster in the Col scaffold (12 mg/mL), whereas the Odex (30 mg/mL)/Col (6 mg/mL) scaffold exhibited the lowest apoptosis index. Furthermore, the expression level of vascular endothelial growth factor (VEGF) mRNA in the group without LMN was higher than that with LMN, and the Odex (30 mg/mL)/Col (6 mg/mL) scaffold without LMN had the highest VEGF protein secretion, allowing the cells to survive and function effectively. Odex/Col scaffolds, with or without LMN, are proposed as a tissue engineering construct to improve HUVEC survival and function for angiogenesis. John Wiley and Sons Inc. 2023-06-13 /pmc/articles/PMC10317976/ /pubmed/37408870 http://dx.doi.org/10.1002/elsc.202200140 Text en © 2023 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sarvestani, Fatemeh Sabet
Tamaddon, Ali‐Mohammad
Yaghoobi, Ramin
Geramizadeh, Bita
Azarpira, Negar
Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title_full Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title_fullStr Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title_full_unstemmed Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title_short Biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
title_sort biocompatible scaffolds based on collagen and oxidized dextran for endothelial cell survival and function in tissue engineering
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317976/
https://www.ncbi.nlm.nih.gov/pubmed/37408870
http://dx.doi.org/10.1002/elsc.202200140
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