Healing and Angiogenic Properties of Collagen/Chitosan Scaffolds Enriched with Hyperstable FGF2-STAB® Protein: In Vitro, Ex Ovo and In Vivo Comprehensive Evaluation
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F21%3AN0000067" target="_blank" >RIV/00027162:_____/21:N0000067 - isvavai.cz</a>
Výsledek na webu
<a href="https://www.mdpi.com/2227-9059/9/6/590" target="_blank" >https://www.mdpi.com/2227-9059/9/6/590</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/biomedicines9060590" target="_blank" >10.3390/biomedicines9060590</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Healing and Angiogenic Properties of Collagen/Chitosan Scaffolds Enriched with Hyperstable FGF2-STAB® Protein: In Vitro, Ex Ovo and In Vivo Comprehensive Evaluation
Popis výsledku v původním jazyce
Wound healing is a process regulated by a complex interaction of multiple growth factors in-cluding fibroblast growth factor 2 (FGF2). Although FGF2 appears in several tissues engineered studies, its applications are limited due to its low stability both in vitro and in vivo. Here, this shortcoming is overcome by use a unique nine-point mutant of lowthe low molecular weight isoform FGF2 retaining full biological activity even after twenty days at 37 °C. Crosslinked freeze-dried 3D porous collagen-chitosan scaffolds enriched bywith this hyper stable recombi-nant human protein named as FGF2-STAB® are consequently tested in terms of their biocompat-ibility and cytotoxicity in vitro using murine 3T3-A31 fibroblasts, ex ovo on chick chorioallantoic membranes and in vivo on animal model of 3-month old White New Zealand rabbits. Metabolic activity assays indicated the positive effect of FGF2-STAB® already at very low concentrations (0.01 µg/mL). The angiogenic properties monitored ex ovo showed enhanced vascularization of the tested scaffolds. Histological evaluation and gene expression analysis by qRT-PCR proved newly formed granulation tissue at the place of a previous skin defect without significant in-flammation infiltration. This work highlights the safety and biocompatibility of newly devel-oped crosslinked collagen/chitosan scaffolds involving FGF2-STAB® protein. Moreover, these sponges could be used as scaffolds for growing cells in dermis replacement, where neovascular-ization is a crucial parameter for successful skin regeneration.
Název v anglickém jazyce
Healing and Angiogenic Properties of Collagen/Chitosan Scaffolds Enriched with Hyperstable FGF2-STAB® Protein: In Vitro, Ex Ovo and In Vivo Comprehensive Evaluation
Popis výsledku anglicky
Wound healing is a process regulated by a complex interaction of multiple growth factors in-cluding fibroblast growth factor 2 (FGF2). Although FGF2 appears in several tissues engineered studies, its applications are limited due to its low stability both in vitro and in vivo. Here, this shortcoming is overcome by use a unique nine-point mutant of lowthe low molecular weight isoform FGF2 retaining full biological activity even after twenty days at 37 °C. Crosslinked freeze-dried 3D porous collagen-chitosan scaffolds enriched bywith this hyper stable recombi-nant human protein named as FGF2-STAB® are consequently tested in terms of their biocompat-ibility and cytotoxicity in vitro using murine 3T3-A31 fibroblasts, ex ovo on chick chorioallantoic membranes and in vivo on animal model of 3-month old White New Zealand rabbits. Metabolic activity assays indicated the positive effect of FGF2-STAB® already at very low concentrations (0.01 µg/mL). The angiogenic properties monitored ex ovo showed enhanced vascularization of the tested scaffolds. Histological evaluation and gene expression analysis by qRT-PCR proved newly formed granulation tissue at the place of a previous skin defect without significant in-flammation infiltration. This work highlights the safety and biocompatibility of newly devel-oped crosslinked collagen/chitosan scaffolds involving FGF2-STAB® protein. Moreover, these sponges could be used as scaffolds for growing cells in dermis replacement, where neovascular-ization is a crucial parameter for successful skin regeneration.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
40301 - Veterinary science
Návaznosti výsledku
Projekt
<a href="/cs/project/NV17-29874A" target="_blank" >NV17-29874A: Optimalizace nanostrukturálních dermálních náhrad na zvířecím modelu</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Biomedicines
ISSN
2227-9059
e-ISSN
2227-9059
Svazek periodika
9
Číslo periodika v rámci svazku
6
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
29
Strana od-do
—
Kód UT WoS článku
000665273200001
EID výsledku v databázi Scopus
2-s2.0-85107137204