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. 2012 Sep 12;7(9):e44869. doi: 10.1371/journal.pone.0044869

Figure 1. Nephron deficit in germ-line p53−/− and CMp53−/− kidneys.

Figure 1

A, B) p53−/− kidneys exhibit 50% fewer and less complex LTA-positive proximal tubules. Metanephroi were harvested at E11.5, cultured on trans-well filters for 72 h and stained for cytokeratin and LTA. LTA counts were averaged from kidneys collected from at least 4 embryos. Mutant kidneys exhibit significantly fewer LTA+ structures than wild-type kidneys (p<0.005). C) E17.5 kidneys were harvested from embryos from p53+/− crosses, formalin-fixed and sectioned for immunostaining (Methods). Sections were stained with WT1 and cytokeratin antibodies. P53−/− kidneys show paucity of WT1 stained nephrons. D) Kidneys from mice with conditional p53 deletion from Six2+ cap mesenchyme (CMp53−/−). Hypoplasia persists post-natally, shown in P0 kidneys, top panels at 4x. Bottom panels (x10) show fewer Lhx1-positive nascent nephrons (red). At P0, 6/8 (75%) examined CMp53−/− kidneys were hypoplastic compared to wild-type littermate kidneys (n = 8).