Fig. 6

a?f, Delaying gut aging in tert^?/? + Cre fish rescues DNA damage, proliferation and senescence in the kidney marrow when compared to tert^?/? no Cre fish. a, Representative immunofluorescence images of DNA damage staining (left, ?H2AX) and quantification (right, n_WT = 5, ntert?/?noCre = 6 and ntert?/?+Cre = 5 fish) in 9-month-old kidney marrow tissues. b, Quantification of p53 protein levels in 9-month-old kidney extracts analyzed by western blot (n_WT = 6, ntert?/?noCre = 8 and ntert?/?+Cre = 6 fish). c, Representative immunofluorescence images of proliferation staining (left, PCNA) and quantification (right, n = 6 fish per group) in 9-month-old kidney marrow tissues. d, Representative images of SA-?-Gal staining of 9-month-old kidney marrow cryosections. e,f, RT?qPCR analysis of senescence-associated genes ink4a/b (p15/16) (n_WT = 5, ntert?/?noCre = 6 and ntert?/?+Cre = 5 fish) (e) and cdkn1a (p21) (n_WT = 6, ntert?/?noCre = 7 and ntert?/?+Cre = 4 fish) (f) expression in 9-month-old kidney marrow samples. g?i, tert mRNA expression in the gut of tert^?/? fish (tert^?/? + Cre fish) have beneficial hematopoietic effects by reducing kidney marrow inflammation and increasing immune compartment compared to tert^?/? no Cre fish. g, Representative immunofluorescence images of immune cell staining (left, L-plastin) and quantification (right, n_WT = 6, ntert?/?noCre = 6 and ntert?/?+Cre = 7 fish) in the tissue of 9-month-old testes. h, Representative immunofluorescence images of neutrophil staining (left, MPX) and quantification (right, n_WT = 6, ntert?/?noCre = 5 and ntert?/?+Cre = 6 fish) in the tissue of 9-month-old kidney marrow. i, Identification of upregulated (left) or downregulated (right) hallmarks in the kidney marrow of tert^?/? no Cre compared to either WT or tert^?/? + Cre fish based on GSEA. The NES depicts to what degree the pathway genes are overrepresented in WT or tert^?/? + Cre, compared to tert^?/? no Cre fish. Scale bar, 20 µm. The dashed lines delineate the kidney tubules. All data are presented as the mean ± s.e.m. (*P < 0.05; **P < 0.01, ***P < 0.001, using a one-way ANOVA and post hoc Tukey test). The western blot graphs represent the mean ± s.e.m. of p53 normalized by ?-actin band intensities. All RT?qPCR graphs represent the mean ± s.e.m. mRNA fold increase after normalization by rps11 gene expression levels.

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