“…The material was processed to obtain the hAD-MSCs from the stromal vascular fraction, and cell characterization was conducted by flow cytometry analysis (CD105, CD90, CD73 positive markers, and CD45, CD34, CD11b, CD19, HLA-DR negative markers) and by differentiation to adipogenic and osteogenic lineages as in Gojanovich et al [18] hAD-MSCs were cultured and incubated with ODM as previously described. [14,19] Briefly, for all experiments, hAD-MSCs were seeded on tissue culture treated wells, coverslips, or previously sterilized (UV light 20 min) scaffolds at 40,000 cells/cm 2 , and grown in standard culture conditions (DMEM, 10% FBS, 100 U/mL penicillin/streptomycin, 37 • C, 5% CO 2 ) for 7 days. Isolations from three independent donors in young passages (2 to 4) were used.…”