ation markers, similarly to p53 KO MEFs, which indicate that p53 plays a specific regulatory role in osteogenic differentiation program. Since we could not induce terminal differentiation of MEFs in culture to typical osteoblasts, which give rise to Ca2+ precipitates, we have used the multipotent bone marrow stromal cell line, MBA-15, which can be induced to give rise to terminally differentiated osteoblasts, and represent a clonal, homogenous cell population. First, we have knocked-down the expression of p53 in these cells, by sh-RNA. Inhibiting the expression of p53 
in MBA-15 cells resulted in elevated basal levels of both osterix and osteocalcin. Induction towards osteogenic differentiation resulted in prominent Ca2+ precipitate formation in the MBA-15 sh-p53 cells compared to their controls, which exhibited sparse precipitate formation. These results, demonstrating a negative regulatory role of p53 on terminal differentiation of bone marrow stromal cells further support previous data showing a negative regulation of p53 during bone formation, in vivo by using an in vitro model. Thus, p53 negatively regulates key osteogenic transcription factors, resulting in restrained osteogenic differentiation of both MEFs and bonemarrow stromal cells, which correspond to two differentiation stages; while MEFs represent an early stage, reflecting the process of embryonic development, bone-marrow stromal cells are adult p53 Regulates Differentiation 4 p53 Regulates Differentiation progenitor cells, which maintain proper bone differentiation and homeostasis. p53 inhibits the adipogenic differentiation program Our QRT-PCR analysis of multiple key differentiation markers in the MEFs pairs demonstrate, for the first time, elevated expression of the key adipogenic transcription factors PPARc and CEBPa in p53 KO MEFs. This suggests a negative regulation of p53 during adipogenesis, which may implicate a physiological role of p53 in fat metabolism. Therefore, we next aimed at evaluating the role of p53 in adipogenesis. The adipogenesis of MEFs by hormonal induction is a well-established model system for the study of adipocyte differentiation in vitro. In 21927650 order to examine the potential of p53 KO and wt MEFs to undergo adipogenic differentiation, these cells were treated with insulin and dexamethasone, and subjected to QRT-PCR analysis of various key adipogenic differentiation markers, at several time p53 Regulates Differentiation 6 p53 Regulates Differentiation untreated. Western blot analysis was performed for p53 and p21.GAPDH serves as a loading control. Relative expression of PPARc was determined by QRT-PCR. Normalized expression levels in control samples were set to 100%. A similar experiment as AB was performed in sh-p53 and sh-con MEFs. The results of QRT-PCR are presented as a range of two duplicate runs after normalization to HPRT control. MEFssh-p53 cells were induced with adiogenic medium either in the presence of the PPARc inhibitor GW9662, or without it. Adipogenic differentiation was assessed using Oil Red O staining for lipid droplets. doi:10.1371/journal.pone.0003707.g004 repression by p53, p53 KO and wt MEFs were treated with Nutlin-3, a small molecule inhibitor of the murine double minute gene. Treatment of cells with this drug resulted 12484537 in accumulation of p53 and activation of its downregulation target, p21. As demonstrated in p53 negatively regulates myofibroblast/Astragalus polysaccharide custom synthesis smooth muscle differentiation by inhibiting the expression of Myocd p53 Reg
