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Fig. 7. p57Kip2 expression in mesenchyme cells of the medullary interstitium is
dependent on a Wnt7b canonical signaling pathway. (A-T)
The distribution of p57Kip2 was compared in E15.5 kidney sections from
wild-type (A-E,K-O), Wnt7b mutants (F-J) and mutants lacking
β-catenin within the interstitial mesenchyme (P-T). p57Kip2 protein was
present in a subset of medullary interstitium within wild-type kidneys
(nuclear staining in C,M). The interstitial expression of p57Kip2 was lost in
this population in Wnt7b mutants (H), but was retained in podocytes
(asterisk in H). By contrast, Hoxa11 was present throughout the renal
interstitium of wild-type (B) and Wnt7b mutant (G) kidneys. When
p57Kip2 was examined in interstitial cells of β-catenin interstitium
mutants (β-galactosidase-positive from genetic labeling), p57Kip2 was not
expressed in interstitial mesenchyme (R), except in rare cases where cells had
escaped recombination (β-galactosidase-negative cells in insets in Q-S).
Scale bar: 40 µm.