Renal Thrombotic Microangiopathy in Mice with Combined Deletion of Endocytic Recycling Regulators EHD3 and EHD4

Eps15 Homology Domain-containing 3 (EHD3), a member of the EHD protein family that regulates endocytic recycling, is the first protein reported to be specifically expressed in the glomerular endothelium in the kidney; therefore we generated Ehd3 –/– mice and assessed renal development and pathology. Ehd3 –/– animals showed no overt defects, and exhibited no proteinuria or glomerular pathology. However, as the expression of EHD4, a related family member, was elevated in the glomerular endothelium of Ehd3 –/– mice and suggested functional compensation, we generated and analyzed Ehd3 –/–; Ehd4 –/– mice. These mice were smaller, possessed smaller and paler kidneys, were proteinuric and died between 3–24 weeks of age. Detailed analyses of Ehd3 –/–; Ehd4 –/– kidneys demonstrated thrombotic microangiopathy (TMA)-like glomerular lesions including thickening and duplication of glomerular basement membrane, endothelial swelling and loss of fenestrations. Other changes included segmental podocyte foot process effacement, mesangial interposition, and abnormal podocytic and mesangial marker expression. The glomerular lesions observed were strikingly similar to those seen in human pre-eclampsia and mouse models of reduced VEGF expression. As altered glomerular endothelial VEGFR2 expression and localization and increased apoptosis was observed in the absence of EHD3 and EHD4, we propose that EHD-mediated endocytic traffic of key surface receptors such as VEGFR2 is essential for physiological control of glomerular function. Furthermore, Ehd3 –/–; Ehd4 –/– mice provide a unique model to elucidate mechanisms of glomerular endothelial injury which is observed in a wide variety of human renal and extra-renal diseases.


Introduction
Human kidneys filter about 180 liters of blood per day, retaining most of the plasma proteins in blood and allowing passage of water and small molecules into urine. The filtering unit of the kidney, the glomerulus, consists of a network of capillaries covered by specialized visceral epithelial cells, the podocytes, and supported by the mesangial cells in the interstitium. Glomerular capillaries are lined by very specialized glomerular endothelial cells (GEnCs) that possess transendothelial pores or ''fenestrations'' and an overlying negatively charged glycocalyx [1]. GEnCs and podocytes secrete basement membranes which fuse as glomeruli mature to form the glomerular basement membrane (GBM) [2,3].
Collectively, GEnCs, the GBM and podocytes together constitute the glomerular filtration barrier [4][5][6]. Injury to or disruption of any of its constituents compromises the integrity of the glomerular filtration barrier resulting in proteinuria. In the recent years, several critical molecular components of podocytes that are indispensable for glomerular filtration have been identified. A number of human diseases with mutated podocyte components have also been identified and several mouse models have been generated that have facilitated our understanding of podocyte biology [7][8][9][10][11][12][13][14]. In comparison, our knowledge of molecular components of GEnCs has lagged behind. This is largely due to lack of information on functionally-critical glomerular endothelium-restricted proteins and the unavailability of suitable mouse models that exhibit glomerular disease upon deletion of endothelial-expressed genes.
Members of the EHD protein family (EHD1-4) have emerged as critical regulators of endocytic traffic of membrane as well as cell surface receptors [15]. The reported glomerular endotheliumrestricted expression of EHD3 within the kidney [16,17] suggested the possibility that EHD protein-mediated endocytic recycling might contribute to GEnC-specific functions. This possibility was strengthened by recent studies that have implicated EHD proteins in regulating physiological functions in other cell types, including adipocytes [18], cardiomyocytes [19], myocytes [20], hepatic sinusoidal endothelial cells [21] and neuronal cells [22]. Though EHD3 was the first protein shown to be specifically expressed in the glomerular endothelium, to date, its potential role in this context has not been investigated. EHD proteins are characterized by an EH domain at the Cterminus, a nucleotide binding P-loop near the N-terminus and a central coiled-coiled region. The EH domain mediates proteinprotein interactions by binding to the Asn-Pro-Phe (NPF) tri-peptide motif present in interacting proteins and facilitates membrane binding through association with membrane phospholipids [23,24]. The P-loop binds and hydrolyzes ATP at a very slow rate in vitro [25], while the coiled-coiled region participates in oligomerization [26].
To investigate the in vivo functional roles of EHD proteins we have previously employed a gene knockout approach and such studies of Ehd1 and Ehd4 have demonstrated their roles in normal murine development and physiology [27][28]. Deletion of Ehd1 resulted in small testis with male infertility (27), while Ehd4 deletion resulted in small testis with moderate reduction in sperm count (28), indicating a role for EHD1 and EHD4 in male germ cell development/differentiation. Deletion of Ehd1 also leads to embryonic lethality and ocular defects whose severity varies with the genetic background of the mouse strains used (Rainey MA et al., manuscript in preparation). Here, we extended this gene knockout approach to Ehd3; however, Ehd3 -/mice showed no discernable pathology. Upregulation of the expression of EHD4, a related family member, in Ehd3 -/-GEnCs led us to hypothesize that EHD4 functionally compensates for loss of EHD3. We generated Ehd3 -/-; Ehd4 -/mice to test this hypothesis and observed severe glomerular disease in these mice, demonstrating a critical role for EHD3 and EHD4 in glomerular health. This is the first report of a knockout mouse model where deletion of genes with GEnC-enriched expression results in phenotypes similar to human diseases with glomerular endothelial injury as the initiating event.

Results
Generation and characterization of Ehd3 -/mice A recombineering strategy similar to that successfully used to generate Ehd1 and Ehd4 null mice in our earlier studies [27,28], was employed to target the 59untranslated region and the first exon of Ehd3 such that targeted animals would not express EHD3 (Text S1 and Figure S1A). Genotyping by PCR ( Figure S1B) and Western blotting of organ lysates ( Figure S1C) from wild-type (Ehd3 +/+ ), heterozygote (Ehd3 +/-) and homozygous deleted (Ehd3 -/-) mice confirmed successful targeting. Ehd3 -/mice were born at expected Mendelian ratios, were healthy and fertile with body weights comparable to their wild-type littermates ( Figure S1D & S1E).

Developmental regulation of EHD3 expression in renal glomerular endothelium
As lack of a renal phenotype in Ehd3 -/mice was unexpected, we first confirmed that EHD3 is indeed expressed in the wild-type kidney using Ehd3 -/kidney as a negative control. Consistent with a previous report [16], our analysis of adult Ehd3 +/+ mouse kidney sections confirmed predominant EHD3 expression ( Figure 1A) in GEnCs as confirmed by co-staining of these cells with endothelial markers tomato lectin (from Lycopersicon esculentum) ( Figure 1C) and CD31 (data not shown); tomato lectin recognizes N-acetyl glucosamine (GlcNAc) and poly-N-acetyllactosamine on the glomerular endothelium [29]. EHD3 staining was not seen in podocytes which stained strongly with the podocyte protein nephrin, ( Figure 1E); nephrin stained podocytes form a discrete rim surrounding EHD3-positive cells, further confirming EHD3 expression in GEnCs. The absence of staining in Ehd3 -/glomeruli validated the specificity of GEnC-specific EHD3 expression ( Figure 1B, D and F).
We next assessed if EHD3 expression in GEnCs is developmentally regulated. Nephrogenesis in mice begins by embryonic day 11 [3] and glomerular development proceeds through a series of nephric structures morphologically seen as vesicle, comma-and S-shaped, developing capillary loop, and maturing glomerulus stages. Newborn mice show a sub-cortical ''nephrogenic zone'' with easily discernable vesicular, comma and S-shaped nephric structures and an expanding cortex with capillary loop and maturing glomerular stages [30]. Analyses of Ehd3 +/+ kidneys at postnatal day 2 showed EHD3 expression in the capillary loop stage and mature glomeruli ( Figure 1G and H) but not in the earlier nephric stages, indicating that its expression is indeed developmentally regulated.
In view of the endothelium-restricted and developmentallyregulated expression of EHD3 in the kidney, we undertook detailed analyses of Ehd3 -/kidneys to characterize potentially subtle glomerular pathology. However, no detectable glomerular abnormalities were observed in H&E and Periodic Acid Schiff (PAS) stained Ehd3 -/kidney sections ( Figure S2A-D). Immunofluorescence microscopy showed similar patterns of staining of endothelial, mesangial and podocyte markers in both Ehd3 +/+ and Ehd3 -/glomeruli ( Figure S2F-M) and transmission electron microscopic (TEM) analysis of Ehd3 -/kidneys from 8-month old mice showed glomerular endothelial cells with normal fenestrations and intact podocyte foot processes ( Figure S2N-O). Finally, no proteinuria was detected in urine samples from Ehd3 -/mice on SDS-PAGE ( Figure S2E) indicating that the functional integrity of the GBM was unaffected in Ehd3 -/kidneys.

Compensatory increase in EHD4 expression in Ehd3 -/glomerular endothelium
Complete absence of glomerular pathology in Ehd3 -/kidneys despite GEnC-enriched EHD3 expression could reflect a lack of requirement of EHD3 in glomerular development and function, or compensatory upregulation of other EHD proteins in the Ehd3 -/-GEnCs. As no information is available on the relative expression of other EHD proteins in the kidney, we undertook immunostaining analyses to assess if other EHD family members are also expressed in the glomerular endothelium. Immunostaining for EHD1, EHD2 and EHD4 showed relatively low signals in the glomerular endothelium but markedly more prominent staining in spatially distinct regions of the kidney: EHD1 was expressed in the brush-border epithelium of proximal tubules (white arrows in Figure 2A); EHD2 in the endothelium and smooth muscle cells of interlobular arteries (white arrows, Figure 2B) and afferent arterioles (white arrow heads in Figure 2B); and EHD4 in the peritubular capillary endothelium (white arrows in panel Figure 2C). Ehd1 -/and Ehd4 -/kidney sections were used as controls for EHD1 and EHD4 staining, respectively (data not shown); staining without a primary antibody was used as a control for EHD2 staining. Thus, as EHD3 appears to be the predominant GEnC-enriched EHD protein, it is unlikely that lack of glomerular defects in Ehd3 -/mice is due to basal co-expression of other EHD family members.
As previous studies have shown compensatory changes in EHD protein expression upon knockout of individual family members [27][28]31] we examined Ehd3 -/kidneys for upregulation of other EHD protein expression. Immunofluorescence analyses showed lack of appreciable differences in EHD1 or EHD2 expression between Ehd3 +/+ and Ehd3 -/kidney sections ( Figure 3A-B and 3C-D). Notably, while EHD4 expression in the peritubular capillaries was comparable in Ehd3 +/+ and Ehd3 -/kidney sections, a marked increase in EHD4 expression was observed in Ehd3 -/-  glomeruli ( Figure 3E-F). Co-staining with labeled tomato lectin showed that EHD4 was specifically upregulated in the Ehd3 -/-GEnCs ( Figure 3G-J). The selective upregulation of EHD4 in Ehd3 -/-GEnCs suggested that EHD4 might functionally compensate for Ehd3 deletion and account for lack of glomerular pathology.

Combined deletion of Ehd3 and Ehd4 in mice leads to renal pathology with proteinuria
To test the hypothesis that a compensatory increase in EHD4 expression prevents the appearance of glomerular pathology in Ehd3 -/mice, we intercrossed Ehd3 -/mice with the previously described Ehd4 -/mice [28,31] to generate Ehd3 -/-; Ehd4 -/doublenull mice. Ehd3 -/-; Ehd4 -/mice were smaller ( Figure 4A), displayed markedly pale ( Figure 4B) and smaller kidneys ( Figure 4C), developed severe proteinuria ( Figure 4D) and died between 3-24 weeks of age. As expected, both EHD3 and EHD4 staining was absent in Ehd3 -/-; Ehd4 -/kidneys ( Figure 4E-H). Interestingly, EHD2 expression was upregulated in the glomerular and peritubular capillary endothelium of Ehd3 -/-; Ehd4 -/kidneys ( Figure 4K-L). Ehd3 -/-; Ehd4 -/mice did not show an upregulation of EHD1 in the glomerular or peritubular capillary endothelium ( Figure 4I-J), but showed increased EHD1 expression at the proximal tubule brush border epithelium. Overall, these results indicate that concurrent deletion of Ehd3 and Ehd4 leads to renal pathology. Ehd3 -/-; Ehd4 -/mice develop thrombotic microangiopathy H&E and PAS staining of kidney sections from Ehd3 -/-; Ehd4 -/mice showed lesions characteristic of thrombotic microangiopathy (TMA). TMA is a lesion observed in a number of human diseases including pre-eclampsia, hemolytic uremic syndrome and malignant hypertension and is defined by the primary locus of injury in the endothelium [32]. Although the majority of human cases of TMA exhibit variable numbers of thrombi, a percentage of cases do not. For example, pre-eclampsia, which has the characteristic lesions of TMA, rarely exhibits thrombi. A diagnosis of TMA is based on a set of characteristic morphologic findings irrespective of the presence of glomerular or arteriolar thrombi. These lesions include endothelial cell swelling, expansion of the subendothelial zone, duplication of the GBM, mesangial cell interposition and evidence of red cell destruction. PAS stained Ehd3 -/-; Ehd4 -/mouse kidney sections showed characteristic glomerulomegaly, thickening and duplication of the GBM, expanded and lyticappearing mesangium, variable degrees of mesangial interposition and abnormal capillary loops ( Figure 5A-B). Other changes included tubular dilation and protein reabsorption droplets in proximal tubules. The glomerular changes were more easily visible with the Jones Methenamine silver stain ( Figure 5C-D). Notably, we did not observe any thrombi in the Ehd3 -/-; Ehd4 -/mouse kidney sections analyzed despite other hallmarks of TMA.
In order to assess the ultrastructural alterations in glomerular endothelial cells of Ehd3 -/-; Ehd4 -/mice, we performed TEM of kidney sections. Endothelial cells with a normal pattern of fenestrations (black arrow heads, Figure 6A and Ai), podocytes with intact foot processes (white arrows, Figure 6A and Ai) and normal GBM were identified in Ehd3 +/-; Ehd4 +/kidneys ( Figure 6A and Ai) and in kidney sections from Ehd3 -/-; Ehd4 +/and Ehd3 +/-; Ehd4 -/mice (data not shown), indicating that the presence of at least one copy of Ehd3 or Ehd4 gene was sufficient to assure ultrastructurally normal glomerular capillaries.
In contrast, TEM of Ehd3 -/-; Ehd4 -/kidney sections ( Figure 6B-D) revealed swollen glomerular endothelial cells without fenestrations, podocytes with variable segmental foot process effacement and thickening and lamellation of GBM (t, Figure 6B, Bi and D) with widening of subendothelial zones containing ''flocculent material'' (f, Figure 6C), lucencies within mesangial areas suggesting lysis (m, Figure 6C) and variable mesangial interposition (i, Figure 6C). Many glomerular endothelial cells contained numerous small structures that looked like abnormal endosomes or vacuoles ( Figure 6B, Bi and Figure 6D, black arrows). These structures were never observed in kidneys from littermate controls. Other changes observed included electron dense deposits in mesangial areas (data not shown), vacuolation within the mesangium and platelet aggregation (p, Figure 6D) within capillary lumens. It is interesting to note that marked pathology was seen not only in endothelial cells but also in podocytes and mesangial cells within the glomeruli. Characteristic lesions of TMA were seen in all Ehd3 -/-; Ehd4 -/kidneys analyzed (at ages of day 17 (d17), d22, d23, d39, d45 and d180), while the only 6 month old animal showed cellular infiltration and collagen deposition as additional renal changes (data not shown). The observed lesions were strikingly similar to that seen in human TMAs like pre-eclampsia and in mouse models with reduction of podocyte-expressed VEGF [32][33][34].
Staining and distribution of endothelial, podocytic and mesangial markers were drastically altered in Ehd3 -/-; Ehd4 -/glomeruli To further characterize the lesions observed by light microscopy and TEM, we performed immunostaining for glomerular cell type markers. The staining patterns of podocyte markers nephrin and synaptopodin were severely altered in Ehd3 -/-; Ehd4 -/glomeruli with loss of the lobulated staining pattern seen in control Ehd3 +/-; Ehd4 +/glomeruli ( Figure 7A-D). Tomato lectin staining of GEnCs and desmin staining of mesangial cells showed markedly altered expression patterns; Ehd3 -/-; Ehd4 -/glomeruli had fewer lectin-positive endothelial cells ( Figure 7E-F) and desmin expression was greatly upregulated in the glomeruli and interstitium when compared to littermate controls ( Figure 7G-H). These studies indicate that concurrent deletion of Ehd3 and Ehd4 adversely affects all glomerular cell types.

Discussion
Studies reported here describe the generation and characterization of a mouse model in which concurrent deletion of two endocytic recycling regulatory proteins, EHD3 and EHD4, results in renal thrombotic microangiopathy (TMA), a pathological lesion commonly seen in diverse clinical conditions. TMA is also seen in pre-eclampsia, a condition that affects about 5% of all pregnancies and is thus the most common glomerular disease in the world [32]. Irrespective of the clinical condition, the initiating event in TMA is thought to be an insult or injury to the endothelium. Though research in recent years has remarkably increased our understanding of the cell types in the glomeruli, much is still unknown about the glomerular endothelial cell. Whole-body deletion of endothelial-expressed genes in mice often results in embryonic lethality precluding analyses of endothelial cell function in the maturing glomerulus. A limited set of genes have recently been shown to be specifically expressed in the glomerular endothelium [16,17], however, knockout mouse models of these genes have not been described. The lack of suitable animal models describing glomerular endothelial disease upon genetic deletion of genes specifically expressed in the glomerular endothelium has hampered research into this important cell type in the renal glomerulus. Thus, our studies reporting a gene knockout mouse model that recapitulates features of human TMA represents a major step forward that should facilitate mechanistic and pharmacological explorations of glomerular endothelial injury.
Since we were unable to find unaltered endothelium in the double null mice of various ages analyzed, our results suggest that processes regulated by EHD proteins are critical to glomerular endothelial health. In view of the extensive changes in the endothelial compartment, together with endothelial-specific expression of EHD3 (and increased endothelial EHD4 in Ehd3 -/glomeruli), it is reasonable to suggest that the changes seen in  podocytes and mesangial cells are likely to be secondary to endothelial defects caused by deletion of Ehd3 and Ehd4. This is not unexpected as cell types within the glomerulus communicate via soluble mediators; elegant studies have shown that injury to any one cell type could compromise the functional integrity of other cell types and the glomerulus as a whole [35,[37][38][39]. For example, soluble factors such as platelet derived growth factor (PDGF) BB elaborated by healthy endothelial cells have been shown to be critical to mesangial health [37] and this might explain the mesangial changes seen in Ehd3 -/-; Ehd4 -/mice. It is also possible that the observed alterations in VEGFR2 expression in glomerular endothelial cells (Figure 8) might affect their health and secondarily contribute to the podocyte pathology seen. Future studies to delete Ehd3 and Ehd4 in a cell type-specific manner (endothelium or podocytes) using specific Cre-recombinase expressing transgenic mouse lines will help unequivocally distinguish the direct versus indirect effects of endothelial EHD3 and EHD4 loss on the podocyte. Towards this end, we have generated double Ehd3 fl/fl ; Ehd4 fl/fl mice that should allow such experiments to be carried out in the future.
The TMA observed in Ehd3 -/-; Ehd4 -/glomeruli bear a striking resemblance to that seen in mouse models with reduced podocyte VEGF expression and a recent mouse model with inducible whole-body deletion of VEGFR2 [40]. This is especially Error bars indicate standard deviation (**indicates P,0.05 using two-tailed analysis). doi:10.1371/journal.pone.0017838.g008 significant since our genetic manipulations were not aimed at altering the levels of VEGF or its receptors, VEGFR1 and VEGFR2 expressed in the glomerular endothelium. The marked alterations in VEGFR2 expression in glomerular endothelial cells and the increased apoptosis seen in Ehd3 -/-; Ehd4 -/glomeruli, however point to a possible role for EHD proteins in the endocytic traffic of VEGFR2 and subsequent regulation of VEGF mediated signaling in the glomeruli. It has been demonstrated that at steady state VEGFR2 localizes to the cell surface and intracellular vesicles presumed to be sorting endosomes [41]. In response to VEGF addition, recycling of intracellular VEGFR2 to the cell surface increases to allow higher VEGF binding and signaling [41,42]. Since EHD3 [26] and EHD4 [43] are both known to regulate trafficking out of sorting endosomes, and in view of the appearance of abnormal vesicular structures in endothelial cells as seen by TEM, it is possible that altered recycling of VEGFR2 out of sorting endosomes in Ehd3 -/-; Ehd4 -/glomerular endothelial cells might impair VEGF signaling resulting in the phenotypes we observe. It is noteworthy that no differences in VEGFR1 staining were noticed between Ehd3 -/-; Ehd4 -/and control glomeruli. This is not surprising as VEGFR1 trafficking has not been shown to be regulated by endocytic regulators in the early or recycling pathway; hence we would not expect Ehd3 and Ehd4 deletion to affect trafficking of VEGFR1.
While we have not yet found a relevant endothelial cell system to analyze whether VEGFR2 distribution and expression pattern in Ehd3 -/-; Ehd4 -/mice might reflect its altered endocytic traffic, studies of individual siRNA-mediated knock-down of EHD3 [26] or EHD4 [43] in HeLa cells indicate that they control traffic of transferrin receptor out of sorting endosomes to a recycling compartment and double knock-down of EHD3 and EHD4 has an identical effect (data not shown). As VEGFR2 has been shown to reside in a sorting endosomal compartment and to recycle to the cell surface upon VEGF stimulation [41,42], absence of EHD3 and EHD4 in glomerular endothelial cells might be expected to impose a block to its recycling and thus disrupt its signaling.
Given the roles of EHD proteins in regulating endocytic recycling, it is likely that loss of EHD3 and EHD4 causes aberrant trafficking of key receptors such as VEGFR2, that are critical for maintenance of glomerular endothelial cell function and endothelial-cell dependent inter-cellular signaling critical for glomerular health. Thus, further studies using the experimental model described here should help link the basic cell biological processes of endocytic traffic, sorting and recycling of such receptors to the pathogenesis of endothelial injury which is an integral part of a number diseases of substantial human health importance.

Breeding and maintenance of mice colonies
Male and female Ehd3 +/mice were crossed to generate Ehd3 +/+ , Ehd3 +/and Ehd3 -/mice. To generate Ehd3 -/-; Ehd4 -/mice, the previously described Ehd4 -/mice [28] were mated to Ehd3 -/mice to generate Ehd3 +/-; Ehd4 +/mice and these were intercrossed to give rise to Ehd3 -/-; Ehd4 -/mice. Animals were genotyped by tail PCR and ink-tattooed on toes for identification. Primer sequences for PCR genotyping are available on request. All experiments involving animals were approved by the University of Nebraska Medical Center Institutional Animal Care and Use Committee and carried out under the approved IACUC protocol number 07-061-FC12. All animals were treated humanely in accordance with institutional guidelines and that of the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals.

Analyses of proteinuria
Urine from mice of indicated genotypes was assayed for proteinuria using a dip-stick method with Albustix (Siemens). Urine samples were boiled for 5 minutes in equal volumes of 2X sample buffer and 0.8 to 2 ml was loaded on a 7.5% SDS-PAGE gel. Bovine serum albumin (BSA) was used as a positive control. Following separation of proteins, the gel was stained using Coomassie Brilliant Blue and images were scanned following destaining in water.

Electron Microscopy
Kidneys were fixed in a 2.0% paraformaldehyde/2.5% glutaraldehyde phosphate buffered fixative, secondarily fixed with 1% osmium tetroxide, dehydrated using a graded acetone series and infiltrated using Polybed 812 epoxy resin. Blocks were polymerized at 60uC. Sections were thinned at 70 nm and stained using uranyl acetate and lead stains followed by scanning under a JEOL 1230 transmission electron microscope. Digital images were taken using a KeenView high-resolution camera and Soft Imaging Solutions AnalySIS ITEM digital software.

TUNEL
For TUNEL assay, 3 mm neutral buffered formalin fixed kidney sections from d17, d23 and d45 Ehd3 -/-; Ehd4 -/mice and littermate controls were deparaffinized and following antigen retrieval, an In Situ Cell Death Detection kit, POD (Roche) was used for TUNEL assay which was performed following the manufacturer's instructions. Appropriate negative and positive controls were included in each experiment. Confocal images of TUNEL were acquired with a LSM510 fluorescence confocal microscope (Carl Zeiss, Thornwood, NY) under either a 63X objective. TUNEL positive cells were counted from 12 sections (1 section/kidney, 2 kidneys/mice, 3 mice/genotype) and plotted. Figure S1 Generation and characterization of Ehd3 -/mice. (A) Partial restriction map of the murine Ehd3 locus, the targeting vector and the mutated Ehd3 loci is depicted. LoxP sequences were inserted to flank the first exon such that it could be deleted by Cre/loxP-mediated recombination. Black rectangles represent exons; black and grey triangles represent loxP and FRT sequences, respectively. RI, EcoRI; H, HindIII. (B) Samples of tail DNA from 10 day old mice were genotyped by PCR. Three primers were used in a single duplex PCR reaction to amplify the WT Ehd3 allele (377 bp) and the deleted allele (488 bp), and the products were separated by agarose gel electrophoresis to determine one of three genotypes of mice carrying various Ehd3 alleles. (C) Western blotting of organ lysates from Ehd3 mice. Fifty mg aliquots of organ lysates from three month-old Ehd3 wild-type (Ehd3 +/+ ), heterozygote (Ehd3 +/-) and null (Ehd3 -/-) male mice were subjected to Western blotting with antisera raised against human EHD proteins as described under Materials and Methods. The membrane was serially probed beginning with EHD3, followed by EHD1 and EHD4 and then EHD2 antibodies. The * denotes bleed-through from the previous blot. In the kidney and brain lysates, the anti-EHD3 antibody recognizes smaller sized products that may represent tissue-specific alternate spliced products of EHD3 lacking the first exon or they may be non genotypes were run on a 7.5% SDS-PAGE and stained using Coomassie Blue. Gels were scanned following de-staining. Bovine serum albumin (BSA) was used as a positive control (lanes 2 and 3). MWM = molecular weight marker (lane 1). Lanes 1-6 were run on the same gel but were noncontiguous. (N-O) Electron micrographs of glomeruli from 8 month old Ehd3 +/+ and Ehd3 -/mice are shown. Endothelium with fenestrations (black arrows) and podocytes with intact foot processes are seen in Ehd3 +/+ and Ehd3 -/mice. Scale bar = 2 mm.

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Text S1 Supporting Information Materials and Methods (DOC)