Fig. 4: CNPs protect against apoptosis by restoring the redox homeostasis.

a Flow cytometry results of HK-2 cells after treatment with vehicle and DDP with or without CNPs; cells were stained with Annexin V-FITC/PI. Representative images are shown. nā=ā3 independent experiments. b Proportion of normal, necrosis, early apoptosis, and late apoptosis in HK-2 cells. nā=ā3 independent experiments. c Western blot analysis of the cleaved PARP (clv-PARP) and cleaved caspase-3 (clv-caspase-3) levels in HK-2 cells after different treatments. GAPDH served as a loading control. nā=ā2 independent experiments. d Representative TUNEL staining images in kidneys. nā=ā3 independent mouse kidneys. Scale bar: 100āμm. The red dotted line indicates the boundary between the kidney edge and background, and the white dotted line represents the boundary between the renal cortex and the medulla. e Quantification of TUNEL positive cells in the respective groups. nā=ā3 independent mouse kidneys, P(DDP)ā=ā0.0015, P(0.5 CNPs)ā=ā0.0035, P(1.5 CNPs)ā=ā0.0016. f ROS content in HK-2 cells detected by flow cytometry analysis after different treatments. Representative images are shown. nā=ā3 independent experiments. g Statistical results of ROS level in HK-2 cells from each group. nā=ā3 independent experiments, P(DDP)ā=ā1.8Eā06, P(DDP+CNPs)ā=ā4.5Eā06. h, i Detection of SOD activities (h) and MDA levels (i) in HK-2 cells after different treatments. nā=ā3 independent experiments. In h, P(DDP)ā=ā0.0206, P(DDP+CNPs)ā=ā0.0233; in i, P(DDP)ā=ā0.0015, P(DDP+CNPs)ā=ā0.00297. j, k Relative mRNA expressions of antioxidant gene HO-1 (j) and pro-oxidant gene NOX2 (i) in the renal cortex of mice from each group. nā=ā3 independent experiments. In j, P(DDP)ā=ā0.00034, P(0.5 CNPs)ā=ā0.00016, P(1.5 CNPs)ā=ā3.2Eā05; in k, P(DDP)ā=ā0.0026, P(1.5 CNPs)ā=ā0.0043. Data are presented as meansā±āSEM., *Pā<ā0.05, **Pā<ā0.01, ***Pā<ā0.001, #Pā<ā0.05, ##Pā<ā0.01, ###Pā<ā0.001; one-way ANOVA with multiple comparisons test. Source data are provided as a Source Data file.