Essential role of Skp2-mediated p27 degradation in growth and adaptive expansion of pancreatic β cells
J. Clin. Invest. Lingwen Zhong, et al. 117:2869
doi:10.1172/JCI32198 [Go to this article.]

Figure 1
Deletion of Skp2 resulted in the accumulation of p27 protein in pancreatic islet cells. (A and B) Pancreatic sections from 3-week-old Skp2+/– (A) and Skp2–/– (B) mice were immunostained with anti-mouse insulin (green) and anti-mouse p27 (red) antibodies. Original magnification, ×20. Arrows in A show β cells that do not express p27 in wild-type islets. Arrows in B show high levels of accumulated p27 in β cells in Skp2–/– islets. (C) Immunoblot analysis of p27 and phospho-p27 (p-p27) expression in the islet cells isolated from Skp2+/– and Skp2–/– pancreata. Graph demonstrates densitometric analysis of immunoblot of p27 and phospho-p27 normalized to tubulin. For all panels, data are representative of 3 experiments.