Effect of diamond-like carbon doped with chromium on cell differentiation, immune activation and apoptosis
Language English Country United States Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
33253412
DOI
10.22203/ecm.v040a17
PII: vol040a17
Knihovny.cz E-resources
- MeSH
- Actins metabolism MeSH
- Alkaline Phosphatase genetics metabolism MeSH
- Apoptosis drug effects immunology MeSH
- Cell Adhesion drug effects MeSH
- Cell Differentiation drug effects immunology MeSH
- Cell Line MeSH
- Chromium pharmacology MeSH
- Cytokines metabolism MeSH
- Diamond pharmacology MeSH
- Fibroblasts cytology drug effects MeSH
- Collagen Type I genetics metabolism MeSH
- Humans MeSH
- Macrophages drug effects metabolism MeSH
- Mesenchymal Stem Cells cytology drug effects immunology metabolism MeSH
- Mice MeSH
- Osteogenesis drug effects MeSH
- Osteocalcin genetics metabolism MeSH
- Cell Count MeSH
- Cell Proliferation drug effects MeSH
- Core Binding Factor Alpha 1 Subunit genetics metabolism MeSH
- Gene Expression Regulation drug effects MeSH
- RNA metabolism MeSH
- Cell Shape drug effects MeSH
- Calcium metabolism MeSH
- Vinculin metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Actins MeSH
- Alkaline Phosphatase MeSH
- Chromium MeSH
- Cytokines MeSH
- Diamond MeSH
- Collagen Type I MeSH
- Osteocalcin MeSH
- Core Binding Factor Alpha 1 Subunit MeSH
- RNA MeSH
- Calcium MeSH
- Vinculin MeSH
Diamond-like carbon (DLC) is a biocompatible material that has many potential biomedical applications, including in orthopaedics. DLC layers doped with Cr at atomic percent (at.%) of 0, 0.9, 1.8, 7.3, and 7.7 at.% were evaluated with reference to their osteoinductivity with human bone marrow mesenchymal stromal cells (hMSCs), immune activation potential with RAW 264.7 macrophage-like cells, and their effect on apoptosis in Saos-2 human osteoblast-like cells and neonatal human dermal fibroblasts (NHDFs). At mRNA level, hMSCs on DLC doped with 0.9 and 7.7 at.% of Cr reached higher maximum values of both RUNX2 and alkaline phosphatase. An earlier onset of mRNA production of type I collagen and osteocalcin was also observed on these samples; they also supported the production of both type I collagen and osteocalcin. RAW 264.7 macrophages were screened using a RayBio™ Human Cytokine Array for cytokine production. 10 cytokines were at a concentration more than 2 × as high as the concentration of a positive control, but the values for the DLC samples were only moderately higher than the values on glass. NHDF cells, but not Saos-2 cells, had a higher expression of pro-apoptotic markers Bax and Bim and a lower expression of anti-apoptotic factor BCL-XL in proportion to the Cr content. Increased apoptosis was also proven by annexin V staining. These results show that a Cr-doped DLC layer with a lower Cr content can act as an osteoinductive material with relatively low immunogenicity, but that a higher Cr content can induce cell apoptosis.
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