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New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon
BMC Nephrology volume 17, Article number: 98 (2016)
Disruption of ROBO2 in humans causes vesicoureteral reflux (VUR)/congenital anomalies of the kidney and urinary tract (CAKUT). PiggyBac (PB) is a DNA transposon, and its insertion often reduces—but does not eliminate—gene expression. The Robo2 insertion mutant exhibited non-dilating VUR, ureteropelvic junction obstruction (UPJO) not found in reported models. We studied the incidence and outcomes of VUR/CAKUT in this mutant and explored the relationship between Robo2 gene expression and the occurrence and severity of VUR/CAKUT.
The urinary systems of newborn mutants were evaluated via Vevo 770 micro-ultrasound. Some of the normal animals—and all of the abnormal animals—were followed to adulthood and tested for VUR. Urinary obstruction experiments were performed on mice with hydronephrosis. The histology of the kidney and ureter was examined by light microscopy and transmission electron microscopy. Robo2 PB/PB mice were crossed with Hoxb7/myr-Venus mice to visualize the location of the ureters relative to the bladder.
In Robo2 PB/PB mice, PB insertion led to an approximately 50 % decrease in Robo2 gene expression. The most common (27.07 %, 62/229) abnormality was non-dilating VUR, and no statistically significant differences were found between age groups. Approximately 6.97 % displayed ultrasound-detectable CAKUT, and these mice survived to adulthood without improvement. No severe CAKUT were found in Robo2 PB/+ mice. The refluxing ureters showed disorganized smooth muscle fibers, reduced muscle cell populations, intercellular edema and intracytoplasmic vacuoles in smooth muscle cells. Both UPJ and UVJ muscle defects were noted in Robo2 PB/PB mice.
Robo2 PB/PB mice is the first Robo2-deficient mouse model to survive to adulthood while displaying non-dilating VUR, UPJO, and multiple ureters with blind endings. The genetic background of these mutants may influence the penetrance and severity of the CAKUT phenotypes. VUR and other CAKUT found in this mutant had little chance of spontaneous resolution, and this requires careful follow-up. We reported for the first time that the non-dilated refluxing ureters showed disorganized smooth muscle fibers and altered smooth muscle cell structure, more accurately mimicking the characteristics of human cases. Future studies are required to test the role of Robo2 in the ureteric smooth muscle.
Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common causes of renal failure in childhood  and represent approximately 30 % of all prenatally diagnosed malformations . CAKUT are phenotypically variable and can affect the kidney(s) and/or the lower urinary tract. Vesicoureteral reflux (VUR) is the most common congenital urinary tract abnormality in childhood and has been associated with an increased risk of urinary tract infection (UTI) and renal scarring, known as reflux nephropathy (RN) . Ureteropelvic junction obstruction (UPJO) is the leading cause of hydronephrosis in children.
CAKUT results from faulty urinary tract development, a process for which numerous genes are critical. ROBO2, a member of the immunoglobulin gene superfamily, is a receptor for the ligand SLIT2. SLIT2-ROBO2 signaling is important for axon guidance during development , and both human studies and animal models have provided evidence for an association between the interruption of ROBO2 and VUR/CAKUT [5–9].
Lu et al. report the disruption of ROBO2 in one patient with a balanced translocation and a phenotype that included VUR, ureterovesical junction (UVJ) defects, and megaureter . In addition, heterozygous point mutations in ROBO2 have been identified in many patients with nonsyndromic VUR [6, 10]. However, some studies [11–14] have been unable to validate the association between ROBO2 and human VUR. Heterozygous mutations have recently been identified in patients with UPJO, posterior urethral valve (PUV) or multicystic dysplastic kidney (MCDK) .
Robo2-deficient mouse models have been used to explore the pathogenesis of Robo2 in CAKUT [5–7]. Studies have shown that SLIT2-ROBO2 signaling plays a key role both in normal ureteric budding and in the reciprocal induction of nephrogenesis by negatively regulating GDNF/RET activity . Robo2 homozygotes had multiplex, dysplastic kidneys and short ureters and died within 48 h of birth [5–7]. Possibly due to variable Robo2 gene dosage, the mosaic mice had broad-spectrum CAKUT phenotypes including renal dysplasia, short ureter, megaureter, abnormally located UVJ and hydronephrosis [6, 7]. Of the long-surviving heterozygotes, 4/26 (15 %) exhibited unilateral megaureter and a wide-open UVJ . Other phenotypes reported in patients with ROBO2 mutations, such as UPJO, PUV and non-dilating VUR, were not found in these models.
PiggyBac (PB) is a DNA transposon. Its insertion often reduces but does not eliminate gene expression, facilitating the identification of specific genetic functions , and it is a mutagen suitable for large-scale mutagenesis in mice. The Institute of Developmental Biology and Molecular Medicine at Fudan University performed a large-scale PB insertional mutagenesis and identified one Robo2 insertion mutant. This mutant was both viable and fertile, and it exhibited non-dilating VUR, UPJO, and ureterovesical junction obstruction (UVJO) that were not found in reported models or other CAKUT phenotypes. We study the incidence and outcomes of VUR/CAKUT in this mutant and explore the relationship between Robo2 gene expression and the occurrence and severity of VUR/CAKUT.
The PB transposon was inserted in the first intron of Robo2 on mouse chromosome 16, nucleotide 74379378. The insertion direction was opposite the gene location. Robo2 PB/PB mice were crossed with Hoxb7/myr-Venus mice, which have been described previously , to visualize the location of the ureters relative to the bladder, as performed previously [18, 19].
Mapping the PB-inserted Robo2 allele
Offspring with the transposon inserted into the Robo2 gene were genotyped by polymerase chain reaction (PCR) amplification using the primers P3 (5′-CTGAGATGTCCTAAATGCACAGCG-3′), P4 (5′-AAGATTCCCTTTCCATGCAGAAGAG-3′) and P5 (5′-GTGTACAGGAGTTTGGCACTGG-3′). Robo2 PB/PB and Robo2 PB/+ were amplified by P3 and P5, which produced a 614 bp fragment. Wild type and Robo2 PB/+ were amplified by P4 and P5, which yielded an 864 bp fragment. PCR conditions were as follows: initial denaturation at 93 °C for 90 s; 40 cycles of 93 °C for 30 s, 57 °C for 30 s, and 65 °C for 2 min; and a final extension at 65 °C for 10 min. Genomic DNA extracted from mouse toes was used as template.
Ultrasound investigation of the urinary system
The urinary system was examined by a Vevo 770 high-frequency micro-ultrasound system. Mice were anesthetized with 2.5 % isoflurane in 1 L/min oxygen via nose cone. A heat lamp was used to keep mice warm during anesthesia. A chemical depilatory was used to remove the fur above the position of the kidneys, and ultrasound gel was generously applied directly to the depilated surface. Next, the real-time micro visualization (RMV) transducer was placed on the ultrasound gel along the spine to identify the kidneys. RMV-708 was used for newborn mice, and RMV-712 was used for juvenile and adult mice. Grossly observable phenotype were described as severe CAKUT.
VUR and urinary tract obstruction experiments
Operators who were blinded to the genotypes performed the VUR test. Mice were dissected using an anterior midline incision to expose the kidneys and the urinary tract. The bladder was punctured with a 25 gauge needle to manually inject methylene blue (1 mg/ml in PBS) at a rate of 100 μl/min until the dye exited through the urethra . The severity of VUR was determined by the extent of the ureter dilation. Combined with ultrasound results, VUR was divided into dilating VUR and non-dilating VUR. To test for urinary tract obstruction, the renal pelvis was microinjected with dye, and its passage along the urinary tract was monitored to determine whether there was evidence of impaired flow along the tract .
Kidneys with attached ureters and bladders were removed from the euthanized mice. Tissue samples were fixed in 4 % paraformaldehyde, embedded in paraffin, sectioned at 4 μm, stained with hematoxylin and eosin (H & E) and Masson’s trichrome and examined under a light microscope.
Sections of the kidney from wild type and Robo2 PB/PB mice (VUR and renal dysplasia) were immunostained for ROBO2 (the EnVision method). ROBO2 was detected using a rabbit polyclonal anti-ROBO2 antibody (1:50; Santa Cruz Biotechnology, Inc.).
For transmission electron microscopy, ureters and renal cortices were cut into small pieces (<1 mm3) and rapidly fixed in 2.5 % glutaraldehyde, then washed in phosphate buffer (pH 7.4), post-fixed in 1 % osmium tetroxide in the same phosphate buffer and dehydrated in increasing concentrations of alcohol and embedded in araldite. The ultrathin 70 nm sections were cut on an ultramicrotome, collected on copper grids, stained with uranyl acetate and lead citrate, and examined by transmission electron microscopy (Philips CM120). RFP and GFP fluorescence were monitored and photographed using an epifluorescence stereomicroscope (MZFLIII; Leica).
Real-time quantitative PCR (qRT-PCR)
The human metanephric kidney is functional at approximately 11 gestational weeks, which corresponds to embryonic stages E15.5-E16.5 in mice. Total RNA from E15.5 embryos was extracted using TRIzol (Invitrogen, USA), and cDNA was prepared with the RNA PCR Kit (TaKaRa). The mixture was incubated for 15 min at 37 °C and 5 s at 85 °C. The qRT-PCR was performed with an All-in-One qPCR Mix Detection Kit (GeneCopoeia) on the Mx3000P Quantitative PCR System (Stratagene) to detect Robo2 expression with the primers P1/P2 located within exons 1 and 2. GAPDH was used as an internal control. The reaction conditions were set as follows: an initial denaturation step of 10 min at 95 °C followed by 40 cycles (10 s at 95 °C, 20 s at 60 °C, and 15 s at 72 °C) with a final elongation step of 5 min at 72 °C. Quantification was performed by measuring the threshold cycle (CT value) and using a standard curve as a reference. The primer sequences were as follows: 5′-GCGGATCTTTATTCTTTTTGCG-3′ (sense) and 5′-TCCTTTTTCCAGTAGATGGTTG-3′ (antisense) for Robo2, and 5′-TGTTCCTACCCCCAATGTGTCC-3′ (sense) and 5′-GGAGTTGCTGTTGAAGTCGCAG-3′ (antisense) for GAPDH.
ROBO2 protein analysis
Kidney and brain proteins were extracted in RIPA buffer with freshly added 1 mM PMSF and 1× proteinase inhibitor (Roche). Next, they were quantified with the BCATM Protein Assay Kit (Pierce). Equal protein were separated by SDS/PAGE and transferred onto PVDF membranes. ROBO2 expression was detected using an anti-ROBO2 antibody (ab64158; 1:1,000) as the primary antibody and biotin-conjugated goat anti-rabbit IgG (CoWin Biotech Co; 1:10,000) as the secondary antibody. SuperSignal West Pico Chemiluminescent Substrate (Thermo 34080) was used for detection and GAPDH levels were used as loading controls (CoWin Biotech Co; 1:500).
All of the statistical analyses were performed using SPSS Version 19. A statistical analysis of the RNA results was performed using Student’s t-test. The prevalence of categorical variables was analyzed using the Chi-square test. Statistical significance was set at P < 0.05.
Genetic characterization of Robo2 mutant mice
The PB transposon was inserted into the first intron of the Robo2 gene (Fig. 1a). In E15.5 embryos, quantitative PCR showed that transcript levels from homozygotes (Robo2 PB/PB) were reduced by approximately 50 % compared to wild-type (Robo2 +/+) littermates. There was no significant difference between heterozygotes (Robo2 PB/+) and wild-type littermates (Fig. 1b). Western blots showed that ROBO2 protein levels were decreased in the brain tissues and kidneys of adult Robo2 PB/PB mice (Fig. 1c), consistent with the quantitative PCR results. Expression of ROBO2 in the control kidneys was higher than in Robo2 PB/PB mice. Expression of ROBO2 in the refluxing kidney was higher than in the kidney of renal dysplaisa (Fig. 1d).
The incidence of urinary malformation in Robo2 mutant mice
The urinary systems of all the newborn Robo2 mutant mice were evaluated using a Vevo 770 micro-ultrasound. Some of the normal mice and all of the abnormal mice were followed to adulthood. All mice were tested for VUR. Urinary obstruction experiments were performed on the mice with hydronephrosis after the VUR test.”
The Vevo 770 micro-ultrasound showed that 6.97 % (16/229) of newborn Robo2 PB/PB mice (8 males, 8 females) displayed diverse urinary malformations, including hydronephrosis, duplex kidneys and dilated ureter (Panel A from Fig. 2). They survived to adulthood without improvement (Panel B from Fig. 2). Compared to wild-type mice (Fig. 3a–d, i–k), non-dilating VUR was more requent in Robo2 PB/PB mice (Fig. 3e–h, l–p) (27.07 % versus 6.84 %, P = 0.000, Chi-squared = 19.65). There were no differences in simple VUR prevalence between age < 60 days and age > 60 days (27.07 % versus 32.50 %, P > 0.05, Chi-squared = 0.71) in Robo2 PB/PB mice, and no gender (P > 0.05, Chi-squared = 0.42) or side (P > 0.05, Chi-squared = 0.70) biases were observed. In summary, urinary malformations were found in 34.06 % (78/229) of Robo2 PB/PB mice, and non-dilating VUR (27.07 %, 62/229) was recognized as the most common abnormality. Grossly identifiable urinary malformations were not found in heterozygotes (N = 127).
Gross anatomy, histology and outcomes of the affected ureters and kidneys in Robo2 PB/PB mice with non-dilating VUR
Compared to the histopathological analysis of the intravesical ureter in a wild-type mouse without VUR (Fig. 3b–d), normal UVJ location and ureteral orifice without dilation (Fig. 3f) were observed in a Robo2 PB/PB mouse with bilateral VUR. Paraffin-embedded sections of refluxing ureters showed normal gross structure, but contained disorganized smooth muscle fibers at the level of the bladder (arrowheads in Fig. 3g). In addition, urothelium was found to partially occlude the lumen, but cellular atypia was not obvious, and cell layer was similar to that of the control, so malignant hyperplasia was not considered (Fig. 3g). Examination by transmission electron microscopy showed both normal general structure and reduced muscle cell population (Fig. 3h). The muscle layer showed intercellular edema (arrow in Fig. 3h) and intracytoplasmic vacuoles (arrowheads in Fig. 3h) in smooth muscle cells.
For a more detailed analysis of the kidney and ureter abnormalities, kidneys and ureters from newborn Robo2 +/+; Hoxb7/myr-Venus (Fig. 3i-k) and Robo2 PB/PB; Hoxb7/myr-Venus (Fig. 3l-p) mice were visualized by fluorescence microscopy. The kidneys were normal in size, and inner diameter of the refluxing ureter from a Robo2 PB/PB; Hoxb7/myr-Venus mouse was wilder than the contralateral ureter (Fig. 3m-n). However, the connection of the ureter relative to the bladder appeared normal (Fig. 3o–p).
To assess the progression of renal damage, we evaluated kidneys from adult Robo2 PB/PB mice with VUR and found no signs of RN (Fig. 4g–h). The kidneys were examined by transmission-electron microscopy, revealing a normal glomerular structure (Fig. 4i).
Gross anatomy, histology and outcomes of the affected ureters in Robo2 PB/PB mice with other CAKUT phenotypes
Dissection revealed that Robo2 PB/PB mice had diverse CAKUT phenotypes (Table 1), including UVJO (Fig. 2b), UPJO (Fig. 2c), duplex kidneys (Fig. 2d) and renal hypo/dysplasia (Fig. 2e-h). No obvious malformations of the genital tracts were observed in any genotype, and different phenotypes were observed within one litter. Of the grossly abnormal phenotypes, 62.5 % (10/16) were on the left, 37.5 % (6/16) were on the right, and none were bilateral.
The anatomy of the renal hypo/dysplasia in Robo2 PB/PB mice was characterized by two distinct patterns. One was hydronephrosis with a markedly dilated renal calyx and nearly complete loss of renal parenchyma (Fig. 2e–f and h). The other was an abnormally small kidney (Fig. 2g). Renal hypo/dysplasia was likely to coexist with other phenotypes (Fig. 2e–h). The dysplastic kidney was grossly cystic, and the contralateral kidney appeared grossly normal with no evidence of hydronephrosis.
Overall, 13/15 Robo2 PB/PB mice with grossly identifiable urinary malformations were found to have concomitant VUR. VUR was not observed in one mouse with renal hypo/dysplasia or in one mouse with malformed UVJs located laterally in the bladder (Fig. 2b). The VUR test was unsuccessful in one mouse that had severe malformation of the urinary tract.
In one mouse with unilateral hydronephrosis, reflux was first found in the contralateral ureter (Fig. 5a), and ipsilateral VUR (Fig. 5b) was then noted to occur with hydronephrosis. The affected mice displayed dilated renal pelvis without any dilatation of the ureter or the UVJ, indicating stenosis at the level of the UPJ. We subsequently examined the histology of the UPJ. The UPJ sections showed dilated ureters and distortion of the smooth muscle (Fig. 5c) compared to UPJ sections of wild-type mice (Fig. 5e). Transmission electron microscopy revealed separated muscle cells and excessive collagen in the UPJ (Fig. 5d).
The UVJ in Robo2 PB/PB mice with UVJO connected to a caudal site in the bladder close to the urethra, causing dilated ureter (Fig. 5h). Histological analysis confirmed the dilation of the distal ureter in the mutant and showed a thinner or a thicker layer of smooth muscle (Fig. 5g). Kidneys and ureters were illuminated because of the PB [Act-RFP] transgene and the Hoxb7/myr-Venus transgene. A Robo2 PB/PB; Hoxb7/myr-Venus newborn mouse exhibited dysplastic cysts in the left kidney, dilated left ureter, and abnormal left UVJ (Fig. 5i-j).
We described a new Robo2-deficient mouse model in the FVB/N background. FVB/N is a VUR-resistant strain . A PB insertion partially disrupted the expression of Robo2, decreasing it to 50 % of the normal level. The realtime PCR results only showed a downward trend in Robo2 transcription in Robo2 PB/+ mice, possibly due to limited data. Robo2 PB/PB mice are the first Robo2-deficient mouse model to survive to adulthood while displaying non-dilating VUR, UPJO, and multiple ureters with blind endings. Most of these phenotypes have been reported in patients with ROBO2 variants [6, 10, 15, 22]. These urinary malformations mimicked human CAKUT and did not follow a typical Mendelian pattern, as do most CAKUT found in children. More than one CAKUT phenotype can be observed in the same individual (human or mouse), demonstrating the need for a careful assessment of the kidneys and urinary tracts . We performed ultrasound screening and followed abnormal mice to adulthood. Because the prevalence of severe CAKUT phenotypes was relatively low, this approach improved the utility of this animal model. This analysis also indicated that Robo2 PB/PB mice preferentially developed unilateral, severe urinary malformations with little chance of spontaneous resolution. Because Robo2 has also been reported to play roles in the development of the brain , lungs  and heart , we examined the morphology of these organs, but we did not observe any obvious defects (data not shown).
The prevalence of urinary malformations in Robo2 PB/PB mice was 34.06 %, higher than the 7.87 % in Robo2 PB/+ mice and the 6.84 % in wild-type mice. Non-dilating VUR was the most common abnormality. Approximately 6.97 % of Robo2 PB/PB mice displayed severe CAKUT phenotypes that were not found in Robo2 PB/+ mice. After dissection, Robo2 PB/PB mice showed renal hypo/dysplasia at a rate of 4.37 % renal hypo/dysplasia, duplex systems at 2.18 % duplex system and VUR and other urinary malformations at 31.44 % VUR and other urinary malformations were found in Robo2 PB/PB mice. Conventional Robo2 mutants with severe degrees of gene deletion showed severe CAKUT bilaterally and with a higher incidence CAKUT . Eliminating the effect of strain and genetic background differences, our results may suggest that the expression level of Robo2 (type of mutation) influences the penetrance and severity of VUR/CAKUT.
Primary VUR is a congenital defect with an UVJ anomaly. In secondary VUR, the valvular mechanism is intact and healthy to start with but becomes overwhelmed by raised vesicular pressures associated with obstruction. The obstructions may be anatomical or functional. UVJ histological defects were noted in Robo2 PB/PB mice. Grossly identifiable urinary malformations with concomitant VUR are unilateral in our models. Therefore, we assume that the VUR found in our models are primary VUR.
Additional factors might predispose mice to diverse urinary malformations. Genetic factors may be influenced by environmental exposure, leading to differing phenotypes despite identical gene mutations [26, 27]. Studies are needed to identify environmental factors that influence the penetrance and severity of CAKUT.
For a more detailed analysis of the kidney and ureter abnormalities, light microscopy evaluation and transmission electron microscopy, respectively, were used. Robo2 PB/PB mice were crossed with Hoxb7/myr-Venus mice to visualize the location of the ureters relative to the bladder. The results were compared with the controls and previously published results.
Unlike the dilated and incompetent UVJ that led to high-grade VUR and hydronephrosis in most Robo2 del5/del5 mice (5), most Robo2 PB/PB mice with simple VUR had normal macroscopic UVJ morphology and lacked hydronephrosis. We found disorganized smooth muscle fibers with intercellular edema and decreased numbers of muscle cells with intracytoplasmic vacuoles in the refluxing intravesical ureters. Most severe CAKUT phenotypes were accompanied by VUR. The ureter histological defects were severe in mice with VUR and renal hypo/dysplasia. Reduced and irregular ureteral smooth muscle staining was reported in Robo2 del5/del5 homozygotes before ureteral dilatation . This mutant is the first mutant in which the histology of the refluxing ureter was similar to the following findings from the intravesical ureteric specimens of VUR patients: smooth muscle disarrangement [28, 29] and intercellular edematous and intracytoplasmic vacuoles [30, 31]. A significant correlation between the grades and smooth muscle lesions [31, 32], widely absent smooth musculature , and a replacement of muscle bundles with connective tissue  have also been reported in VUR patients. These structural changes may result in the deformation of the architecture of the ureteric wall smooth muscle layer.
Paraffin sections of refluxing Robo2 PB/PB mouse kidneys displayed no signs of inflammation or scarring. A previous study demonstrated that sterile reflux alone fails to induce reflux nephropathy . This may explain why our mutants showed no signs of inflammation or scarring. Structural alteration in the podocyte foot process was found in a Robo2 podocyte-specific knockout mouse . Our electron micrograph shows normal glomerular structure that may be due to the remaining expression of ROBO2.
It has been reported that chronic kidney damage is significantly related to congenital renal hypo/dysplasia, rather than to infections and VUR [36, 37]. Genetic factors may influence both the occurrence of dysplasia and the propensity for scar formation . In our models, 4.37 % of homozygous mutants had histologically demonstrated renal hypo/dysplasia. Some of these may be secondary effects of hydronephrosis; however, some maybe congenital and require careful followed-up.
Both UPJ and UVJ histological defects were noted in Robo2 PB/PB mice. Histopathological analysis revealed dilation of the ureter, distortion of the smooth muscle, separated muscle cells with intracytoplasmic vacuoles and excessive collagen. These pathological findings may be secondary effects of hydronephrosis.
The ureteral smooth muscles play a crucial role in ureteral peristalsis  and UVJ formation . Sufficient contraction of the ureteric muscular layer by closing the ureteric orifice prevents VUR . It was speculated that the disorganization of the muscular layer leads to a malfunctioning valve system and causes VUR . One study has indicated that congenital obstructions might be due to aberrant ureteric smooth muscle organization, resulting in impaired peristalsis . Future studies are required to provide additional mechanistic insights into the role of Robo2 in ureteric smooth muscle cells in the development of UPJ and UVJ. Mechanistic studies investigating the role of Robo2 in smooth muscle cell function, proliferation, and migration are needed. Based on previous studies [42–44], we speculate that ROBO2 in ureteric smooth muscle cells interacts with Ab1, permitting Enabled (Ena)/vasodilator-stimulated phosphoprotein (VASP) protein phosphorylation and thus participating in the cytoskeletal changes in smooth muscle α-actin.
VUR could be caused by defects in ureteric budding, ureter differentiation and elongation, peristalsis, UVJ formation, and bladder and urethra development . Mackie and Stephens proposed the ureteric bud theory  that the UB must emerge from the ND at the precise site to invade the MM for normal kidney development to occur. If budding occurs rostral or caudal to this site, would lead to renal hypoplasia/dysplasia and ectopic insertion of the ureter into the bladder, resulting in VUJ obstruction and VUR. Multiple ureteric buds may lead to short duplex ureters, duplex kidneys, ectopic and dysplastic kidneys . We speculate that quantitative differences in either Gdnf or genes within the Robo2/Slit network are most likely responsible for the urinary tract defects we observe. Other factors such as environment factors, may conribute to this process.
There are several limitations to this study. We did not examine how the different anomalies arose, and more work is needed to explain why Robo2 PB/PB mice preferentially develop unilateral severe urinary malformations.
The genetic background of the Robo2 mutants discussed may influence the penetrance and severity of the CAKUT phenotypes. Genetic factors may be influenced by environmental exposure, leading to differing phenotypes. This mutant is the first Robo2-deficient mouse model to survive to adulthood while displaying non-dilating VUR, UPJO, and multiple ureters with blind endings. VUR and other CAKUT in this mutant showed very low rates of spontaneous resolution after birth. We may uncover more deleterious mutations in the Robo2 gene if we focus on the DNA analysis of patients with these phenotypes. CAKUT associated with genetic mutations may indicate poor prognosis, and patients with Robo2 mutations should therefore be followed up closely. We first reported that the non-dilated refluxing ureters showed disorganized smooth muscle fibers and altered smooth muscle cell structure, more accurately mimicking the characteristics of human cases. Future studies are required to test the role of Robo2 in ureteric smooth muscle. Robo2 PB/PB mice could be used as an animal model to better understand both urinary tract development and the cellular and molecular mechanisms of Robo2 in the kidney.
CAKUT, Congenital anomalies of the kidney and urinary tract; H & E, hematoxylin and eosin; MCDK, multicystic dysplastic kidney; PCR, polymerase chain reaction; PUV, posterior urethral valve; qRT-PCR, Real-time quantitative PCR; RMV, real-time Micro Visualization; RN, reflux nephropathy; UPJO, Ureteropelvic junction obstruction; UTI, urinary tract infection; UVJ, ureterovesical junction; VUR, Vesicoureteral reflux
Neild GH. What do we know about chronic renal failure in young adults? I. Primary renal disease. Pediatr Nephrol. 2009;24(10):1913–9.
Toka HR, Toka O, Hariri A, Nguyen HT. Congenital anomalies of kidney and urinary tract. Semin Nephrol. 2010;30(4):374–86.
Mattoo TK. Vesicoureteral reflux and reflux nephropathy. Adv Chronic Kidney Dis. 2011;18(5):348–54.
Dickson BJ, Gilestro GF. Regulation of commissural axon pathfinding by slit and its Robo receptors. Annu Rev Cell Dev Biol. 2006;22:651–75.
Grieshammer U, Le M, Plump AS, Wang F, Tessier-Lavigne M, Martin GR. SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site. Dev Cell. 2004;6(5):709–17.
Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, et al. Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. Am J Hum Genet. 2007;80(4):616–32.
Wang H, Li Q, Liu J, Mendelsohn C, Salant DJ, Lu W. Noninvasive assessment of antenatal hydronephrosis in mice reveals a critical role for robo2 in maintaining anti-reflux mechanism. PLoS One. 2011;6(9):e24763.
Fan X, Li Q, Pisarek-Horowitz A, Rasouly HM, Wang X, Bonegio RG, et al. Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure. Cell Rep. 2012;2(1):52–61.
Ji J, Li Q, Xie Y, Zhang X, Cui S, Shi S, et al. Overexpression of Robo2 causes defects in the recruitment of metanephric mesenchymal cells and ureteric bud branching morphogenesis. Biochem Biophys Res Commun. 2012;421(3):494–500.
Bertoli-Avella AM, Conte ML, Punzo F, de Graaf BM, Lama G, La Manna A, et al. ROBO2 gene variants are associated with familial vesicoureteral reflux. J Am Soc Nephrol. 2008;19(4):825–31.
Dobson MG, Darlow JM, Hunziker M, Green AJ, Barton DE, Puri P. Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux. Kidney Int. 2013;84(2):327–37.
Cordell HJ, Darlay R, Charoen P, Stewart A, Gullett AM, Lambert HJ, et al. Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux. J Am Soc Nephrol. 2010;21(1):113–23.
Zu S, Bartik Z, Zhao S, Sillen U, Nordenskjold A. Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux. Pediatr Nephrol. 2009;24(8):1501–8.
Sanna-Cherchi S, Reese A, Hensle T, Caridi G, Izzi C, Kim YY, et al. Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds. J Am Soc Nephrol. 2005;16(6):1781–7.
Hwang DY, Dworschak GC, Kohl S, Saisawat P, Vivante A, Hilger AC, et al. Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract. Kidney Int. 2014;85(6):1429–33.
Ding S, Wu X, Li G, Han M, Zhuang Y, Xu T. Efficient transposition of the piggyBac (PB) transposon in mammalian cells and mice. Cell. 2005;122(3):473–83.
Chi X, Hadjantonakis AK, Wu Z, Hyink D, Costantini F. A transgenic mouse that reveals cell shape and arrangement during ureteric bud branching. Genesis. 2009;47(2):61–6.
Miller MM, Iglesias DM, Zhang Z, Corsini R, Chu L, Murawski I, et al. T-cell factor/beta-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney disease. Kidney Int. 2011;80(2):146–53.
Murawski IJ, Myburgh DB, Favor J, Gupta IR. Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/− mouse. Am J Physiol Renal Physiol. 2007;293(5):F1736–45.
Murawski IJ, Watt CL, Gupta IR. Assessing urinary tract defects in mice: methods to detect the presence of vesicoureteric reflux and urinary tract obstruction. Methods Mol Biol. 2012;886:351–62.
Murawski IJ, Maina RW, Malo D, Guay-Woodford LM, Gros P, Fujiwara M, et al. The C3H/HeJ inbred mouse is a model of vesico-ureteric reflux with a susceptibility locus on chromosome 12. Kidney Int. 2010;78(3):269–78.
van Eerde AM, Duran K, van Riel E, de Kovel CG, Koeleman BP, Knoers NV, et al. Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. PLoS One. 2012;7(4):e31327.
Kidd T, Brose K, Mitchell KJ, Fetter RD, Tessier-Lavigne M, Goodman CS, et al. Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors. Cell. 1998;92(2):205–15.
Englund C, Steneberg P, Falileeva L, Xylourgidis N, Samakovlis C. Attractive and repulsive functions of Slit are mediated by different receptors in the Drosophila trachea. Development. 2002;129(21):4941–51.
Qian L, Liu J, Bodmer R. Slit and Robo control cardiac cell polarity and morphogenesis. Curr Biol. 2005;15(24):2271–8. doi:10.1016/j.cub.2005.10.037.
Nordenskjold A. Genetic Aspects of Congenital Urologic Anomalies. Eur Urol Suppl. 2015;14(1):2–8.
Williams G, Fletcher JT, Alexander SI, Craig JC. Vesicoureteral reflux. J Am Soc Nephrol. 2008;19(5):847–62.
Gearhart JP, Lee BR, Partin AW, Epstein JI, Gosling JA. A quantitative histological evaluation of the dilated ureter of childhood. II: Ectopia, posterior urethral valves and the prune belly syndrome. J Urol. 1995;153(1):172–6.
Oswald J, Brenner E, Schwentner C, Deibl M, Bartsch G, Fritsch H, et al. The intravesical ureter in children with vesicoureteral reflux: a morphological and immunohistochemical characterization. J Urol. 2003;170(6 Pt 1):2423–7.
Izol V, Acikalin AA, Kuyucu Y, Deger M, Aridogan IA, Polat S, et al. Ultrastructural and immunohistopathological evaluation of intravesical ureters via electron and light microscopy in children with vesicoureteral reflux. J Urol. 2014;191(4):1110–7. doi:10.1016/j.juro.2013.10.038.
Sofikerim M, Sargon M, Oruc O, Dogan HS, Tekgul S. An electron microscopic examination of the intravesical ureter in children with primary vesico-ureteric reflux. BJU Int. 2007;99(5):1127–31.
Arena S, Fazzari C, Arena F, Scuderi MG, Romeo C, Nicotina PA, et al. Altered ‘active’ antireflux mechanism in primary vesico-ureteric reflux: a morphological and manometric study. BJU Int. 2007;100(2):407–12.
Oswald J, Schwentner C, Brenner E, Deibl M, Fritsch H, Bartsch G, et al. Extracellular matrix degradation and reduced nerve supply in refluxing ureteral endings. J Urol. 2004;172(3):1099–102.
Schwentner C, Oswald J, Lunacek A, Schlenck B, Berger AP, Deibl M, et al. Structural changes of the intravesical ureter in children with vesicoureteral reflux-does ischemia have a role? J Urol. 2006;176(5):2212–8.
Bowen SE, Watt CL, Murawski IJ, Gupta IR, Abraham SN. Interplay between vesicoureteric reflux and kidney infection in the development of reflux nephropathy in mice. Dis Model Mech. 2013;6(4):934–41.
Ismaili K, Hall M, Piepsz A, Wissing KM, Collier F, Schulman C, et al. Primary vesicoureteral reflux detected in neonates with a history of fetal renal pelvis dilatation: a prospective clinical and imaging study. J Pediatr. 2006;148(2):222–7.
Montini G, Tullus K, Hewitt I. Febrile urinary tract infections in children. N Engl J Med. 2011;365(3):239–50.
Constantinou CE, Yamaguchi O. Multiple-coupled pacemaker system in renal pelvis of the unicalyceal kidney. Am J Physiol. 1981;241(5):R412–8.
Viana R, Batourina E, Huang H, Dressler GR, Kobayashi A, Behringer RR, et al. The development of the bladder trigone, the center of the anti-reflux mechanism. Development. 2007;134(20):3763–9.
Tanagho EA, Guthrie TH, Lyon RP. The intravesical ureter in primary reflux. J Urol. 1969;101(6):824–32.
Wang GJ, Brenner-Anantharam A, Vaughan ED, Herzlinger D. Antagonism of BMP4 signaling disrupts smooth muscle investment of the ureter and ureteropelvic junction. J Urol. 2009;181(1):401–7.
Tani K, Sato S, Sukezane T, Kojima H, Hirose H, Hanafusa H, et al. Abl interactor 1 promotes tyrosine 296 phosphorylation of mammalian enabled (Mena) by c-Abl kinase. J Biol Chem. 2003;278(24):21685–92.
Woodring PJ, Hunter T, Wang JY. Regulation of F-actin-dependent processes by the Abl family of tyrosine kinases. J Cell Sci. 2003;116(Pt 13):2613–26.
Bashaw GJ, Kidd T, Murray D, Pawson T, Goodman CS. Repulsive axon guidance: Abelson and Enabled play opposing roles downstream of the roundabout receptor. Cell. 2000;101(7):703–15.
Rasouly HM, Lu WN. Lower urinary tract development and disease. Wires Syst Biol Med. 2013;5(3):307–42. doi:10.1002/Wsbm.1212.
Mackie GG, Stephens FD. Duplex kidneys: a correlation of renal dysplasia with position of the ureteral orifice. J Urol. 1975;114(2):274–80.
We thank F. Costantini from Columbia University Medical Center for providing the plasmid Hoxb7/myr-Venus.
This work was supported by the grants from national basic research program of China (973 program 2011CB944001) and national natural science foundation of China (81200487).
Availability of data and materials
All data underlying the findings are within the paper.
HX and X-hW conceptualized the study. J-lL performed the experiment. HX and LS obtained funding. J-lL and LS acquired the data. J-lL, LS and QS analyzed the data. HX, X-hW, J-lL, LS and QS contributed to data interpretation and manuscript preparation. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Ethics approval and consent to participate
All animal procedures were conducted according to the animal care and ethics laws and were approved by the Animal Care Committee of Institute of Developmental Biology and Molecular Medicine at Fudan University (2012020).
Jialu Liu and Li Sun as co-first authors.
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Liu, J., Sun, L., Shen, Q. et al. New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon. BMC Nephrol 17, 98 (2016) doi:10.1186/s12882-016-0308-5