| Summary: | 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 (EC<sub>50</sub> 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 (<i>SOD1</i>), catalase (<i>CAT)</i>, matrix metallopeptidase 1 (<i>MMP1)</i>, transforming growth factor beta 1 (<i>TGFB1)</i>, glutathione peroxidase 1 (<i>GPX1</i>), fibronectin 1 (<i>FN1</i>), hyaluronan synthase 2 (<i>HAS2</i>), laminin subunit beta 1 (<i>LAMB1</i>), lumican (<i>LUM</i>), cadherin 1 <i>CDH1,</i> collagen type IV alpha (<i>COL4A1</i>), fibrillin (<i>FBN</i>), and versican (<i>VCAN</i>)) treated with the lowest non-cytotoxic concentrations in the HaCaT cells after 24 h. The AgNPs were capable of up-regulating only two genes (<i>SOD1</i> and <i>MMP1</i>) while the CNFs were very effective in up-regulating eight genes (<i>FN1, MMP1, CAT, CDH1, COL4A1, FBN, GPX1,</i> and <i>TGFB1</i>) 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.
|
|---|