Ink4a/Arf expression is a biomarker of aging
J. Clin. Invest. Janakiraman Krishnamurthy, et al. 114:1299 doi:10.1172/JCI22475 [Go to this article.]

Figure 2
p16^INK4a expression in specific compartments by immunohistochemistry and cell purification. (A) Immunoperoxidase staining performed on paraffin-embedded sections of germ-line p16^INK4a-deficient (KO), WT young (3.5 months), and WT old (25 months) murine tissues using an anti-p16^INK4a antibody. Positively staining cells demonstrate both nuclear and cytoplasmic expression. GC, germinal center. (B) Relative expression ratios (old/young, log₂ scale) of p16^INK4a in specific compartments (average purity >94% for all fractions) of bone marrow (lin^–, 2%; lin⁺, 97%), spleen (B220⁺, 48%; Mac1⁺, 9%; B220^–Mac1^–, 22%), and lymph node. Asterisks indicate that p16^INK4a expression was undetectable in these cell populations from young mice, and therefore a minimum estimate of the fold increase is shown.