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. 2019 Jun 10;10:2538. doi: 10.1038/s41467-019-10386-8

Fig. 6.

Fig. 6

Cordycepin prevents senescence and SASP, which are NRF2-dependent. a NRF2 and p-NRF2 expression levels in whole cell lysates from cordycepin-treated fibroblasts for the indicated times. This test was repeated three times. Representative images were shown. b NRF2 expression levels in nuclei from cordycepin-treated fibroblasts for the indicated times. c Representative immunofluorescence pictures of NRF2 in control and cordycepin-treated (3 days) fibroblasts. This test was repeated three times. Representative images were shown. d Representative immunofluorescence pictures of NRF2 of the tongues from normal mice and irradiated mice (control, prevention, treatment) 10 days after radiation. e p-NRF2 expression levels in nuclei from cordycepin-treated fibroblasts for the indicated times. f Quantification of mRNA expression for GSTA1, NQO1 and Srx from cordycepin-treated fibroblasts for the indicated times. g GCLC, GCLM, HMOX1 and NQO1 expression levels in whole cell lysates from cordycepin-treated fibroblasts for the indicated times. h Western blot analysis of p16 and p21 levels in irradiated control or cordycepin-treated (3 days) fibroblasts following knockdown of NRF2 7 days after radiation. i Quantification of mRNA expression for senescence secretory phenotype in fibroblasts following knockdown of NRF2 7 days after radiation. j Staining for SA-β-gal 7 days after radiation in fibroblasts following knockdown of NRF2. This test was repeated three times. Representative images were shown. k Representative images of fibroblasts colonies generated in survival assays following knockdown of NRF2. l Analysis of reactive oxygen species (ROS) levels 24 h after radiation in fibroblasts following knockdown of NRF2. Bars represent 50 μm (c), 100 μm (d), 250 μm (j). Data in f, i, and l represent the means ± S.D. (n = 3, *P < 0.05, **P < 0.01; student’s t-test)