Effects of fullerene C60 on the friction and wear characteristics of ceramics in ethanol

For the combinations of a pin of Si₃N₄ and five kinds of disk, the friction and wear test was carried out in ethanol, and in ethanol containing C₆₀ particles (1 wt%). A topographical analysis was also performed on the micro-asperities of the wear surfaces to estimate the behavior of C₆₀ particles, and the degree of surface damage. As a results, the following facts were found. (1) The addition of C₆₀ particles in ethanol decreased the wear rates of such ceramic disks as Al₂O₃, SiC and TiC and of the mating Si₃N₄ pins. (2) The addition of C₆₀ particles decreased the mean coefficient of friction for SiC, Si₃N₄, and TiC disks. (3) The wear rates of pin and disk depended on the topographies of worn surfaces such as the mean depth of micro-grooves, the mean tip radius of micro-asperities and so on.     

Hypoxic Culture Maintains Cell Growth of the Primary Human Valve Interstitial Cells with Stemness

The characterization of aortic valve interstitial cells (VICs) cultured under optimal conditions is essential for understanding the molecular mechanisms underlying aortic valve stenosis. Here, we propose 2% hypoxia as an optimum VIC culture condition. Leaflets harvested from patients with aortic valve regurgitation were digested using collagenase and VICs were cultured under the 2% hypoxic condition. A significant increase in VIC growth was observed in 2% hypoxia (hypo-VICs), compared to normoxia (normo-VICs). RNA-sequencing revealed that downregulation of oxidative stress-marker genes (such as superoxide dismutase) and upregulation of cell cycle accelerators (such as cyclins) occurred in hypo-VICs. Accumulation of reactive oxygen species was observed in normo-VICs, indicating that low oxygen tension can avoid oxidative stress with cell-cycle arrest. Further mRNA quantifications revealed significant upregulation of several mesenchymal and hematopoietic progenitor markers, including CD34, in hypo-VICs. The stemness of hypo-VICs was confirmed using osteoblast differentiation assays, indicating that hypoxic culture is beneficial for maintaining growth and stemness, as well as for avoiding senescence via oxidative stress. The availability of hypoxic culture was also demonstrated in the molecular screening using proteomics. Therefore, hypoxic culture can be helpful for the identification of therapeutic targets and the evaluation of VIC molecular functions in vitro.