Cluster-Assembled Zirconia Substrates Accelerate the Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells.
Sara CastiglioniLaura LocatelliAlessandra CazzanigaFrancesca Maria OrecchioTommaso SantanielloClaudio PiazzoniLionel BureauFrancesca BorghiPaolo MilaniJeanette A MaierPublished in: Nanomaterials (Basel, Switzerland) (2023)
Due to their high mechanical strength and good biocompatibility, nanostructured zirconia surfaces (ns-ZrOx) are widely used for bio-applications. Through supersonic cluster beam deposition, we produced ZrOx films with controllable roughness at the nanoscale, mimicking the morphological and topographical properties of the extracellular matrix. We show that a 20 nm ns-ZrOx surface accelerates the osteogenic differentiation of human bone marrow-derived MSCs (bMSCs) by increasing the deposition of calcium in the extracellular matrix and upregulating some osteogenic differentiation markers. bMSCs seeded on 20 nm ns-ZrOx show randomly oriented actin fibers, changes in nuclear morphology, and a reduction in mitochondrial transmembrane potential when compared to the cells cultured on flat zirconia (flat-ZrO 2 ) substrates and glass coverslips used as controls. Additionally, an increase in ROS, known to promote osteogenesis, was detected after 24 h of culture on 20 nm ns-ZrOx. All the modifications induced by the ns-ZrOx surface are rescued after the first hours of culture. We propose that ns-ZrOx-induced cytoskeletal remodeling transmits signals generated by the extracellular environment to the nucleus, with the consequent modulation of the expression of genes controlling cell fate.
Keyphrases
- extracellular matrix
- dengue virus
- mesenchymal stem cells
- endothelial cells
- photodynamic therapy
- zika virus
- cell fate
- induced apoptosis
- oxidative stress
- dna damage
- high glucose
- cystic fibrosis
- risk assessment
- bone marrow
- gene expression
- genome wide
- reactive oxygen species
- signaling pathway
- high resolution
- cell proliferation
- drug induced
- room temperature
- ionic liquid
- cell migration
- transcription factor
- bone regeneration