Silver Nanoparticles Alone or in Combination with Calcium Hydroxide Modulate the Viability, Attachment, Migration, and Osteogenic Differentiation of Human Mesenchymal Stem Cells.
Almaha S AlgazlanNihal A AlMuraikhiManikandan MuthuranganHanan BaltoFahd M AlsalleehPublished in: International journal of molecular sciences (2022)
This study aimed to evaluate the effect of silver nanoparticles (AgNPs) alone or in combination with calcium hydroxide (Ca(OH) 2 ) on the proliferation, viability, attachment, migration, and osteogenic differentiation of human mesenchymal stem cells (hMSCs). Different concentrations of AgNPs alone or mixed with Ca(OH) 2 were prepared. Cell proliferation was measured using AlamarBlue, and hMSCs attachment to dentin disks was evaluated using scanning electron microscopy. Live-dead imaging was performed to assess apoptosis. Wound healing ability was determined using the scratch-migration assay. To evaluate osteogenic differentiation, the expression of Runt-related transcription factor (RUNX2), Transforming growth factor beta-1 (TGF-β1), Alkaline Phosphatase (ALP), and Osteocalcin (OCN) were measured using real-time reverse transcriptase polymerase chain reaction. ALP staining and activity were also performed as indicators of osteogenic differentiation. AgNPs alone seemed to favor cell attachment. Lower concentrations of AgNPs enhanced cell proliferation. AgNP groups showed markedly less apoptosis. None of the medicaments had adverse effects on wound closure. The expression of TGF-β1 was significantly upregulated in all groups, and OCN was highly expressed in the AgNP groups. AgNPs 0.06% showed the most enhanced ALP gene expression levels, activity, and marked cytochemical staining. In conclusion, AgNPs positively affect hMSCs, making them a potential biomaterial for various clinical applications.
Keyphrases
- silver nanoparticles
- mesenchymal stem cells
- transforming growth factor
- transcription factor
- cell proliferation
- electron microscopy
- umbilical cord
- gene expression
- endothelial cells
- epithelial mesenchymal transition
- bone marrow
- poor prognosis
- cell therapy
- oxidative stress
- wound healing
- high resolution
- cell cycle arrest
- cell death
- signaling pathway
- single cell
- pluripotent stem cells
- induced pluripotent stem cells
- binding protein
- pi k akt
- emergency department
- dna binding
- human health
- flow cytometry
- climate change
- photodynamic therapy
- aqueous solution
- fluorescence imaging
- adverse drug