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Tytuł pozycji:

Benefits in the Macrophage Response Due to Graphene Oxide Reduction by Thermal Treatment.

Tytuł:
Benefits in the Macrophage Response Due to Graphene Oxide Reduction by Thermal Treatment.
Autorzy:
Cicuéndez M; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.
Casarrubios L; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.
Barroca N; Center for Mechanical Technology & Automation (TEMA), Mechanical Engineering Department, University of Aveiro, 3810-193 Aveiro, Portugal.
Silva D; Center for Mechanical Technology & Automation (TEMA), Mechanical Engineering Department, University of Aveiro, 3810-193 Aveiro, Portugal.
Feito MJ; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.
Diez-Orejas R; Departamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Marques PAAP; Center for Mechanical Technology & Automation (TEMA), Mechanical Engineering Department, University of Aveiro, 3810-193 Aveiro, Portugal.
Portolés MT; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.; CIBER de Bioingeniería, Biomateriales y Nanomedicina, 28040 Madrid, Spain.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jun 22; Vol. 22 (13). Date of Electronic Publication: 2021 Jun 22.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Oxidation-Reduction*
Oxidative Stress*
Temperature*
Graphite/*metabolism
Macrophages/*physiology
Animals ; Biomarkers ; Cells, Cultured ; Cytokines/metabolism ; Gene Expression ; Graphite/chemistry ; Inflammation Mediators/metabolism ; Mice ; Microscopy, Atomic Force ; Nanostructures/chemistry ; RAW 264.7 Cells ; Reactive Oxygen Species/metabolism ; Spectrum Analysis
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Grant Information:
NeuroStimSpinal Project, Grant Agreement No. 829060 European Union's Horizon 2020 Research and Innovation Programme (H2020-FETOPEN-2018-2020, NeuroStimSpinal Project, Grant Agreement No. 829060)
Contributed Indexing:
Keywords: cytokine; graphene oxide; immune response; macrophage; reduced graphene oxide
Substance Nomenclature:
0 (Biomarkers)
0 (Cytokines)
0 (Inflammation Mediators)
0 (Reactive Oxygen Species)
0 (graphene oxide)
7782-42-5 (Graphite)
Entry Date(s):
Date Created: 20210702 Date Completed: 20210723 Latest Revision: 20210723
Update Code:
20240105
PubMed Central ID:
PMC8267858
DOI:
10.3390/ijms22136701
PMID:
34206699
Czasopismo naukowe
Graphene and its derivatives are very promising nanomaterials for biomedical applications and are proving to be very useful for the preparation of scaffolds for tissue repair. The response of immune cells to these graphene-based materials (GBM) appears to be critical in promoting regeneration, thus, the study of this response is essential before they are used to prepare any type of scaffold. Another relevant factor is the variability of the GBM surface chemistry, namely the type and quantity of oxygen functional groups, which may have an important effect on cell behavior. The response of RAW-264.7 macrophages to graphene oxide (GO) and two types of reduced GO, rGO15 and rGO30, obtained after vacuum-assisted thermal treatment of 15 and 30 min, respectively, was evaluated by analyzing the uptake of these nanostructures, the intracellular content of reactive oxygen species, and specific markers of the proinflammatory M1 phenotype, such as CD80 expression and secretion of inflammatory cytokines TNF-α and IL-6. Our results demonstrate that GO reduction resulted in a decrease of both oxidative stress and proinflammatory cytokine secretion, significantly improving its biocompatibility and potential for the preparation of 3D scaffolds able of triggering the appropriate immune response for tissue regeneration.
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