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Carbon Nanofibers versus Silver Nanoparticles: Time-Dependent Cytotoxicity, Proliferation, and Gene Expression
dc.contributor.author | Salesa Landete, Beatriz | |
dc.contributor.author | Assis, Marcelo de | |
dc.contributor.author | Andres, Juan | |
dc.contributor.author | Serrano-Aroca, Ángel | |
dc.date.accessioned | 2021-09-29T07:11:55Z | |
dc.date.available | 2021-09-29T07:11:55Z | |
dc.date.issued | 2021-09-03 | |
dc.identifier.citation | Salesa, B.; Assis, M.; Andrés, J.; Serrano-Aroca, Á. Carbon Nanofibers versus Silver Nanoparticles: Time-Dependent Cytotoxicity, Proliferation, and Gene Expression. Biomedicines 2021, 9, 1155. https://doi.org/10.3390/biomedicines9091155 | ca_CA |
dc.identifier.issn | 2227-9059 | |
dc.identifier.uri | http://hdl.handle.net/10234/194847 | |
dc.description | This article belongs to the Special Issue Feature Papers in "Biomedical Materials and Nanomedicine" | |
dc.description.abstract | Carbon nanofibers (CNFs) are one-dimensional nanomaterials with excellent physical and broad-spectrum antimicrobial properties characterized by a low risk of antimicrobial resistance. Silver nanoparticles (AgNPs) are antimicrobial metallic nanomaterials already used in a broad range of industrial applications. In the present study these two nanomaterials were characterized by Raman spectroscopy, transmission electron microscopy, zeta potential, and dynamic light scattering, and their biological properties were compared in terms of cytotoxicity, proliferation, and gene expression in human keratinocyte HaCaT cells. The results showed that both AgNPs and CNFs present similar time-dependent cytotoxicity (EC50 of 608.1 µg/mL for CNFs and 581.9 µg/mL for AgNPs at 24 h) and similar proliferative HaCaT cell activity. However, both nanomaterials showed very different results in the expression of thirteen genes (superoxide dismutase 1 (SOD1), catalase (CAT), matrix metallopeptidase 1 (MMP1), transforming growth factor beta 1 (TGFB1), glutathione peroxidase 1 (GPX1), fibronectin 1 (FN1), hyaluronan synthase 2 (HAS2), laminin subunit beta 1 (LAMB1), lumican (LUM), cadherin 1 CDH1, collagen type IV alpha (COL4A1), fibrillin (FBN), and versican (VCAN)) treated with the lowest non-cytotoxic concentrations in the HaCaT cells after 24 h. The AgNPs were capable of up-regulating only two genes (SOD1 and MMP1) while the CNFs were very effective in up-regulating eight genes (FN1, MMP1, CAT, CDH1, COL4A1, FBN, GPX1, and TGFB1) involved in the defense mechanisms against oxidative stress and maintaining and repairing tissues by regulating cell adhesion, migration, proliferation, differentiation, growth, morphogenesis, and tissue development. These results demonstrate CNF nanomaterials’ unique great potential in biomedical applications such as tissue engineering and wound healing. | ca_CA |
dc.format.extent | 17 p. | ca_CA |
dc.format.mimetype | application/pdf | ca_CA |
dc.language.iso | eng | ca_CA |
dc.publisher | MDPI | ca_CA |
dc.relation.isPartOf | Biomedicines 2021, vol. 9, no 9 | ca_CA |
dc.rights.uri | http://creativecommons.org/licenses/by-sa/4.0/ | ca_CA |
dc.subject | silver nanoparticles | ca_CA |
dc.subject | carbon nanofibers | ca_CA |
dc.subject | human keratinocytes | ca_CA |
dc.subject | cytotoxicity | ca_CA |
dc.subject | proliferation | ca_CA |
dc.subject | gene expression | ca_CA |
dc.title | Carbon Nanofibers versus Silver Nanoparticles: Time-Dependent Cytotoxicity, Proliferation, and Gene Expression | ca_CA |
dc.type | info:eu-repo/semantics/article | ca_CA |
dc.identifier.doi | https://doi.org/10.3390/biomedicines9091155 | |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca_CA |
dc.relation.publisherVersion | https://www.mdpi.com/2227-9059/9/9/1155 | ca_CA |
dc.description.sponsorship | This research was supported by the Fundación Universidad Católica de Valencia San Vicente Mártir, Grant 2020-231-006UCV and by the Ministerio de Ciencia e Innovación (PID2020-119333RB-I00 / AEI / 10.13039/501100011033) (awarded to Á.S.-A.). J.A. is grateful to the Universitat Jaume I for Project UJI-B2019-30, the Generalitat Valenciana for Project AICO2020, and the Ministerio de Ciencia, Innovación y Universidades (Spain) Project PGC2018- 094417-B-I00 for supporting this research financially. M.A. is grateful to the Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP (FAPESP CEPID-Finance Code 2013/07296-2), FINEP, Conselho Nacional de Desenvolvimento Cientifico e Tecnológico-CNPq (Finance Code 166281/2017-4), and CAPES (Finance Code 001). | |
dc.type.version | info:eu-repo/semantics/publishedVersion | ca_CA |
project.funder.name | Fundación Universidad Católica de Valencia San Vicente Mártir | ca_CA |
project.funder.name | Universitat Jaume I | |
project.funder.name | Generalitat Valenciana | |
project.funder.name | Ministerio de Ciencia, Innovación y Universidades | |
project.funder.name | Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP | |
project.funder.name | Conselho Nacional de Desenvolvimento Cientifico e Tecnológico-CNPq | |
project.funder.name | CAPES | |
oaire.awardNumber | 2020-231-006UCV | ca_CA |
oaire.awardNumber | PID2020-119333RB-I00 / AEI / 10.13039/501100011033 | |
oaire.awardNumber | UJI-B2019-30 | |
oaire.awardNumber | AICO2020 | |
oaire.awardNumber | PGC2018- 094417-B-I00 | |
oaire.awardNumber | FAPESP CEPID-Finance Code 2013/07296-2 | |
oaire.awardNumber | 166281/2017-4 | |
oaire.awardNumber | 001 |
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