01 January 1970 0 5K Report

I am currently culturing human dermal microvascular endothelial cells obtained from Lonza and want to proceed with experiments comparing diabetic (CC-2930) vs non-diabetic (CC-2543). I am aware that these are primary cells, however, how can I ensure that during culture, diabetic cells actually retain their characteristics? Should I culture them in high-glucose to mimic in vivo conditions of 'mis-managed' diabetic patients since they are in a state of hyperglycaemia? Is there an assay I can do that would confirm they are diabetic, when compared to healthy control?

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