Supplementary Figure 5: NUP93, NUP205 and XPO5 localize to developing podocytes.
From: Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome
(a–c) Neonatal rat coronal kidney sections at embryonic day 16.5 p.c. were stained with antibodies against NUP93, NUP205 or XPO5 (green) and the podocyte nuclear marker WT1 (red). Note that NUP93 (a) and NUP205 (b) mark nuclear envelopes with a nuclear rim pattern in podocyte precursor cells (arrowheads) at the capillary loop stage and in other cell types in developing kidney. Anti-XPO5 antibody (c) prominently marks the nuclear content of cells in developing kidney with a dot-like pattern (arrow). Scale bars, 25 μm.
