Skip to main content
Fig. 2 | Stem Cell Research & Therapy

Fig. 2

From: KAT6A regulates stemness of aging bone marrow-derived mesenchymal stem cells through Nrf2/ARE signaling pathway

Fig. 2

KAT6A regulated stemness of OBMSCs. a Forty-eight hours later, the transfection efficiency was tested by qRT-PCR after transfection of scrambled siRNA or KAT6A siRNA into YBMSCs (n = 3). b CCK-8 was performed to explore the proliferative capacity of YBMSCs that transfected with scrambled siRNA or KAT6A siRNA (n = 3). c The colony-forming abilities of YBMSCs that transfected with scrambled siRNA or KAT6A siRNA were explored by crystal violet after culture for 12 days (n = 3). d After osteogenic induction for 14 days, expressions of osteogenic-related genes of Runx2, OCN, and BMP2 were detected in YBMSCs that transfected with scrambled siRNA or KAT6A siRNA (n = 3). e After osteogenic induction for 21 days, alizarin red staining was performed in YBMSCs that transfected with scrambled siRNA or KAT6A siRNA (n = 3). f Forty-eight hours later, the transfection efficiency was tested by qRT-PCR after transfection of vector or KAT6A plasmid into OBMSCs (n = 3). g CCK-8 was performed to explore the proliferative capacity of OBMSCs that transfected with vector or KAT6A plasmid (n = 3). h The colony-forming abilities of OBMSCs that transfected with vector or KAT6A plasmid were explored by crystal violet after culture for 12 days (n = 3). i After osteogenic induction for 14 days, expressions of osteogenic-related genes of Runx2, OCN, and BMP2 were detected in OBMSCs that transfected with vector or KAT6A plasmid (n = 3). j After osteogenic induction for 21 days, alizarin red staining was performed in OBMSCs that transfected with vector or KAT6A plasmid (n = 3)

Back to article page