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Diverse effects of lead nitrate on the proliferation, differentiation, and gene expression of stem cells isolated from a dental origin

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Table 1: Changes in trypan blue dye exclusion assay, 3-(4,5-dimethylthiazol-2-yl)-2-,5-diphenyltetrazolium bromide (MTT) assay, and lactate3.13 ± 0.072+dehydrogenase leakage (LDH) rate at various Pbconcentrations (mean2.85 ± 0.72
Table 2: Immunophenotype analysis of bone marrow mesenchymal stem cells (BM-MSCs), dental permanent stem cells (DPSCs), dentaldeciduous stem cells (SCDs), and periodontal ligament stem cells (PDLs), respectively, cultured before and after treatment of PbMS
Figure 2: (a) Conventional qualitative SA-2+experiments, the results represent average of five culture replicates with standard deviation and a representative photomicrograph was given-gal assay by X-gal staining of bone marrow mesenchymal stem cells (BM-M
Figure 3: In vitromatrix deposition stained with von Kossa staining at day 21. Adipogenesis was detected by neutral oil droplet formation stained with OilRed O at day 21
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