“…After the stable MSC lines had been propagated and multiplied, the multipotencyrelated attributes of their random representatives were identified by the ectopic onset of chondrogenic differentiability. The processes of the functional reprogramming of MSCs into chondroblasts/chondrocytes took place in low-glucose-formulated DMEM enriched with 15% FBS (Sigma-Aldrich, Merck, Poznań, Poland), 1× Glutamax (Invitrogen, Thermofisher Scientific, Waltham, Massachusetts, USA), 1% antibiotic-antimycotic solution (AAS; Sigma-Aldrich, Merck, Poznań, Poland), and the cocktail of supplements triggering cytodifferentiation as elaborated by Branly et al (2017). This cocktail comprised 100 nM dexamethasone (Sigma-Aldrich, Merck, Poznań, Poland), 50 μg/mL L-ascorbic acid 2-phosphate (Sigma-Aldrich, Merck, Poznań, Poland), 40 μg/mL L-proline (Sigma-Aldrich, Merck, Poznań, Poland), 1 nM sodium pyruvate (Sigma-Aldrich, Merck, Poznań, Poland), 1% insulin-transferrin-sodium selenite (ITS) solution (Sigma-Aldrich, Merck, Poznań, Poland), and 10 ng/mL transforming growth factor-β1 (TGF-β1; Sigma-Aldrich, Merck, Poznań, Poland).…”