Skip to main content
. 2024 Apr 5;15:2939. doi: 10.1038/s41467-024-47317-1

Fig. 2. Senescent cells accumulate in the sclerotic endplates of LSI mice and aged mice.

Fig. 2

a Representative images of coronal mouse caudal endplate sections of L4/5 stained for SA-βGal (green) at 4 and 8 weeks after LSI or sham surgery (top). Representative immunofluorescent images of tdTom+ cells (red) and DAPI (blue) staining of nuclei at 4 and 8 weeks after LSI or sham surgery in p16tdTom mice (bottom). Quantitative analysis of the number of SA-βGal+ cells (b) or tdTom+ cells (c) of a. d Representative immunofluorescent images of HMGB1+ cells (green) and DAPI (blue) staining of nuclei in endplates at 4 and 8 weeks after LSI or sham surgery. e Quantified fluorescence intensity of HMGB1+ cells of d. f, g Relative expression of senescence pathway genes, Cdkn2a (p16), Trp53 (p53), and Cdkn1a (p21) (f) or typical SASP, II1b (IL-1β) and II6 (IL-6) in the endplates at 4 and 8 weeks after LSI or sham surgery. h Representative images of SA-βGal (green) staining (top) or tdTom+ cells (red) and DAPI (blue) staining of nuclei (bottom) in 3-month-old or 20-month-old mice. i, j Quantitative analysis of h. k Representative immunofluorescent images of HMGB1+ cells (green) and DAPI (blue) staining of nuclei in 3-month-old or 20-month-old mice. l Quantified fluorescence intensity of k. Relative expression of senescence pathway genes (m) or typical SASP (n) in the endplates of 3-month-old or 20-month-old mice. Scale bars, 50 μm. n = 6 per group. Data are represented as means ± standard deviations, as determined by two-tailed Student’s t test or One-way ANOVA. Source data are provided as a Source Data file.