Table 1.
Primer used for qPCR.
Table 2.
Affymetrix gene expression data selected according to function.
Table 3.
qPCR analysis of human podocyte gene expression: Verification of selected microarray results.
Fig 1.
Western-blot analysis of human podocytes: Verification of selected microarray results.
Quantification of total TUBB2B (A), DCDC2 (B), THBS1 (C), COL4A3 (D), SYNPO2 (E) and PCDH9 (F) protein. GAPDH = loading control. For quantification, total protein was normalized with respect to GAPDH (representative example from 3 independent experiments). PAN = puromycin aminonucleoside. EV = everolimus. MeOH = methanol, solvent for EV. p = p-value. Data are means ± SD. ns = not significant.
Fig 2.
Immunofluorescence analysis of human podocytes: Verification of selected microarray results.
(A+B) alpha-tubulin, TUBB2B and DCDC2 images are presented in gray scale for maximum contrast. The merge image depicts TUBB2B and DCDC2 in green and alpha-tubulin in red. DAPI was used to visualize nuclei (blue). PAN-treated cells are smaller compared to control cells, due to alterations of the actin cytoskeleton and cell-substrate adhesion dynamics [7]. (C) Double staining of TUBB2B (red) and DCDC2 (green) of untreated control cells (D+E) Quantification of TUBB2B- and DCDC2 staining intensity with Image J software (n = 3 experiments, ≥ 10 cells per condition). PAN = puromycin aminonucleoside. EV = everolimus. MeOH = methanol, solvent for EV. p = p-value. Data are means ± SD. Scale bar = 50 μm.
Fig 3.
TUBB2B and DCDC2 are expressed in human kidneys.
(A) Western-blot analysis to measure the existence of TUBB2B and DCDC2 in human kidneys. GAPDH = loading control. CC = Podocyte cell culture. WT = Wild type kidney. (B+C) Immunohistochemical staining of TUBB2B and DCDC2 in healthy human kidneys. 3,3'-diaminobenzidine (DAB) was used as chromogen (brown staining) and nuclei were stained with hematoxylin (blue). The black arrows mark a nuclear as well as cytoplasmic staining of TUBB2B and a cytoplasmic staining of DCDC2 in podocytes. A negative control was performed without the primary antibody (S1 Fig). T = tubule. EPC = parietal epithelial cell. Scale bar = 50 μm.
Fig 4.
Periodic acid-Schiff and Wilm’s tumour 1 staining of wild type and Tubb2bbrdp/brdp mouse kidneys (E18.5).
(A+B) Glomeruli were stained with periodic acid-Schiff to highlight basement membranes of glomerular capillary loops and tubular epithelium. (A) Tubb2bbrdp/brdp mice often show a lack in glomerular tuft and capillary lumen development. (B) The capillary loops of the wild type glomeruli are well-defined and thin. Scale bars = 25 μm. (C+D) Wilm’s tumour 1 (Wt1) expression was detectable by immunohistochemistry (dark-brown nuclear staining results from 3,3'-diaminobenzidine). Nuclei were stained with hematoxylin (blue). (C) Tubb2bbrdp/brdp kidneys show a specific Wt1 staining in podocytes (P) arranged in a string of pearls-like pattern at the periphery of the glomerulus, characteristic of an early developmental stage. (D) In the developing wild type kidney, Wt1 is expressed in mesenchymal cells that are starting the mesenchymal-to-epithelial transition (condensing metanephric mesenchyme (M)), in early epithelial structures (comma- (C) and S-shaped (S) bodies) and in fully differentiated epithelial cells (glomerular podocytes (G)). Black asterisks: Enlarged section areas on the right. Scale bars = 50 μm. (E) Percentage of capillary loop stages versus mature glomeruli in 3 mutant and 4 wild type animals. For each animal, 15 to 30 capillary loop stages / mature glomeruli were counted. Data are means ± SD. (F) Average number of Wt1-positive cells per glomerulus in 3 mutant and 4 wild type animals. 15 to 30 glomeruli / animal were counted. Data are means ± SD.
Fig 5.
Nphs2-, Nphs1- and Synpo staining of wild type and Tubb2bbrdp/brdp mouse kidneys (E18.5).
Immunohistochemical staining of mice kidneys (dark-brown Nphs2, Nphs1 and Synpo stainings result from 3,3'-diaminobenzidine. Nuclei were stained with hematoxylin (blue). (A+B) Nphs2 staining. (A) Tubb2bbrdp/brdp kidneys show a specific Nphs2 staining in podocytes arranged like a row of pearls at the periphery of the glomerulus. (B) Within the developing wild type kidney early capillary loop stages and maturing glomeruli are labeled. (C+D) Nphs1 staining. (E+F) Synpo staining. (C-F) Both, Nphs1 and Synpo patterns are comparable to the Nphs2 staining. Black asterisks: Enlarged section areas on the right. Scale bars = 50μm.
Fig 6.
Tubb2b staining of wild type and Tubb2bbrdp/brdp mouse kidneys (E18.5).
Immunohistochemical staining of mice kidneys (dark-brown Tubb2b staining results from 3,3'-diaminobenzidine. Nuclei were stained with hematoxylin (blue). (A) Tubb2bbrdp/brdp kidneys show a specific cytoplasmic Tubb2b expression in tubuli (T) and in podocytes (P), confirming the developmental defects seen with the Wt1, Nphs2, Nphs1 and Synpo stainings. (B) Tubb2b expression in wild type kidneys is restricted to the mature podocytes. Interestingly in the developing wild type kidney Tubb2b is not expressed in the early developmental stages of maturing podocytes. Note, that in murine podocytes nuclear Tubb2b seems much less expressed compared to human kidneys. Black asterisks: Enlarged section areas on the right. Scale bars = 50 μm.
Fig 7.
Transmission electron micrographs of wild type and Tubb2bbrdp/brdp mouse kidneys (E18.5).
(A-F) With TEM, a delay in glomerular endothelial (E) and podocyte (P) development could be observed in Tubb2bbrdp/brdp mice. (A+B) Glomerulus with immature, cuboidal podocytes (black arrow). (C+D) Incompletely differentiated podocyte foot processes (FPs); some are extremely wide and linked by occludens junctions (OJs). (D) The glomerular basement membrane (asterisk) appears to be normal. (A+E) Glomeruli with no or small visible capillary lumen (CL) and multiple endothelial cells within the capillary loops (black arrows). (F) Swollen and vacuolated glomerular endothelial cells with decreased fenestrations. (G-I) Glomeruli of wild type Tubb2b mice had open glomerular capillaries with fenestrated endothelium, differentiated podocyte foot processes linked by SDs (black arrow) and a normal glomerular basement membrane.