In order to explore how S100A8 and S100A9 may participate in the kidney stone formation, we used recombinant S100A8, recombinant S100A9, or recombinant S100A8/S100A9 heterodimer to culture the HK-2 ce
Caco-2 cells (clone TC7) were cultured for 15 days post confluence on plastic dishes to reach the differentiation, then cells were treated for 24h with alpha or gamma tocopherol enriched mixed micelle
