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Abstract

Diabetic nephropathy is characterized by decreased expression of bone morphogenetic protein-7 (BMP-7) and decreased podocyte number and differentiation. Extracellular antagonists such as connective tissue growth factor (CTGF; CCN-2) and sclerostin domain-containing-1 (SOSTDC1; USAG-1) are important determinants of BMP signaling activity in glomeruli. We studied BMP signaling activity in glomeruli from diabetic patients and non-diabetic individuals and from control and diabetic CTGF^+/+ and CTGF^+/− mice. BMP signaling activity was visualized by phosphorylated Smad1, −5, and −8 (pSmad1/5/8) immunostaining, and related to expression of CTGF, SOSTDC1, and the podocyte differentiation markers WT1, synaptopodin, and nephrin. In control and diabetic glomeruli, pSmad1/5/8 was mainly localized in podocytes, but both number of positive cells and staining intensity were decreased in diabetes. Nephrin and synaptopodin were decreased in diabetic glomeruli. Decrease of pSmad 1/5/8 was only partially explained by decrease in podocyte number. SOSTDC1 and CTGF were expressed exclusively in podocytes. In diabetic glomeruli, SOSTDC1 decreased in parallel with podocyte number, whereas CTGF was strongly increased. In diabetic CTGF^+/− mice, pSmad1/5/8 was preserved, compared with diabetic CTGF^+/+ mice. In conclusion, in human diabetic nephropathy, BMP signaling activity is diminished, together with reduction of podocyte markers. This might relate to concomitant overexpression of CTGF but not SOSTDC1. (J Histochem Cytochem 57:623–631, 2009)

Keywords

kidney bone morphogenetic proteins Smads connective tissue growth factor diabetic nephropathy glomerulus podocytes quantitative histochemistry

M any studies have shown a decrease in expression of podocyte differentiation markers and a decrease in the number of podocytes in diabetic nephropathy, but the underlying mechanisms still remain to be identified (Shankland 2006). One critical aspect of podocyte damage in diabetic nephropathy might be a lack of bone morphogenetic protein (BMP) signaling (Wang et al. 2006). BMPs are dimeric molecules that induce signaling through the BMP receptors, a heterotetrameric complex composed of type I and type II serine/threonine kinase receptors. Binding of the BMP ligand to its receptors induces serine phosphorylation of the downstream signaling components Smad1, −5, and −8. Phosphorylated Smad1, −5, and −8 (pSmad1/5/8) translocate to the nucleus and act as transcription factors (Feng and Derynck 2005). Of over 20 BMPs, BMP-7 has by far received most attention in studies of adult renal disease. Although its role and expression pattern in embryology and preclinical models of renal disease are well established, the expression pattern of BMP-7 in the adult human kidney is still a subject of debate (Nguyen and Goldschmeding 2008). Moreover, other BMPs are also expressed in the kidney, and there is increasing evidence for regulation of BMP signaling activity by extracellular BMP antagonists, including connective tissue growth factor (CTGF; CCN-2) and sclerostin domain-containing-1 (SOSTDC1; USAG-1) (Nguyen and Goldschmeding 2008). CTGF and SOSTDC1 are both expressed in human glomeruli (Ito et al. 1998; Blish et al. 2008). Recently, we showed that CTGF inhibits BMP-7 activity in experimental diabetic nephropathy and in cultured renal cells (Nguyen et al. 2008a). Inhibition of CTGF and of SOSTDC1 improved outcome of experimental (non-)diabetic kidney injury, but their relation with BMP signaling activity has not been studied in human diabetic nephropathy (Yanagita et al. 2006; Guha et al. 2007; Nguyen et al. 2008a; Yokoi et al. 2008).

In the present study, we assessed glomerular BMP signaling activity in diabetic nephropathy in relation to SOSTDC1 and CTGF expression, and to podocyte number and differentiation.

Materials and Methods

Human Tissue

Renal tissue from five patients with diabetic nephropathy was selected from the archives of the Department of Pathology of the University Medical Center Utrecht in accordance with the Declaration of Helsinki and the guidelines of the University Medical Center Utrecht. Two out of five diabetic kidneys were transplant kidneys. Patients' age ranged from 54 to 75 years; three patients were women, and two were men. Mean disease duration was 10 years. As controls, tumor-free areas of five human kidneys obtained after surgical nephrectomy were used.

Immunohistochemistry

Tissue samples were formalin-fixed and paraffin-embedded (FFPE). Four-μm-thick sections were used for immunostaining. Primary antibody source, antibody references, antigen retrieval methods, and primary antibody dilutions are shown in Table 1. The PowerVision poly-HRP-anti-rabbit IgG or poly-HRP-anti-mouse/rabbit/rat IgG detection system (ImmunoLogic; Duiven, The Netherlands) was applied to enhance immunoreactivity, using DAB (ImmunoLogic) or NovaRed (Vector; Torrance, CA) as chromogens. For anti-nephrin, rabbit anti-guinea pig-HRP (P0141; Dako Netherlands, Heverlee, Belgium) was used as a secondary antibody before the application of PowerVision as tertiary antibody. Sections were counterstained with hematoxylin. Negative controls were performed by replacing the primary antibody with normal serum of the species in which the primary antibody was raised. Photographs were taken on a Nikon Eclipse E800 microscope with a Nikon DXM1200 digital camera using the Nikon ACT-1 software, version 2.70 (Nikon Netherlands; Lijnden, The Netherlands).

Immunofluorescence

Three-μm-thick FFPE tissue sections were used for immunofluorescent studies (for primary antibody source and dilutions, see Table 1). For anti-synaptopodin, goat anti-mouse FITC was used as secondary antibody (F0479; Dako Netherlands). All other primary antibodies were detected using PowerVision and the TSA tetramethylrhodamine system or TSA fluorescein system (PerkinElmer Life Sciences; Waltham, MA). Nuclear counterstain was performed with TO-PRO-3 iodide (Molecular Probes; Eugene, OR). Double-labeling immunofluorescence was performed as a sequence of two single-immunofluorescent protocols. Photographs were taken with a Leica TCS SP2 confocal microscope (Leica Microsystems; Rijswijk, The Netherlands).

Quantification

The cellular localization of immunoreactivity was examined by three investigators. Globally sclerosed glomeruli were excluded from analysis. Glomeruli were examined at random positions on the slides. The number of positive cells was counted in at least 20 glomeruli per subject. For correlations, WT1 and pSmad1/5/8, as well as WT1 and SOSTDC1, were counted on consecutive sections. The pSmad1/5/8 staining intensity and synaptopodin-positive and nephrin-positive glomerular tuft areas were calculated in at least 20 glomeruli using Adobe Photoshop software, version 10.0 (Adobe Systems; San Jose, CA) and ImageJ software, version 1.39u (National Institutes of Health; Bethesda, MD).

Table 1

Primary antibodies, dilutions, and antigen retrieval methods for immunohistochemistry and immunofluorescence

Antibody to	Source	Dilution IHC/IF	Incubation	Antigen retrieval	Manufacturer	Reference
pSmad1/5/8 (9511 lot 8) ∗h	Rabbit (polyclonal)	1:300/1:50	Overnight, 4C	Citrate	Cell Signaling Technology; Danvers, MA	(Yanagita et al. 2006)
pSmad1/5/8 (9511 lot 8) ∗m	Rabbit (polyclonal)	1:200	Overnight, 4C	EDTA	Cell Signaling Technology	(Yanagita et al. 2006)
CTGF (mc2)	Mouse (monoclonal)	1:50/1:25	1 Hour	EDTA	FibroGen; San Francisco, CA
SOSTDC1	Rabbit (polyclonal)	1:1,000	1 Hour	Citrate	Wake Forest University; Winston-Salem, NC	(Blish et al. 2008)
WT1 (sc-192 lot F0407)	Rabbit (polyclonal)	1:200/1:200	1 Hour	EDTA	Santa Cruz Biotechnologies; Santa Cruz, CA	(Menne et al. 2006)
Synaptopodin (G1D4 lot 711200)	Mouse (monoclonal)	Undiluted	1 Hour	Citrate	PROGEN Biotechnik; Heidelberg, Germany	(Mezzano et al. 2007)
Nephrin (GP-N2 lot 803070)	Guinea pig (polyclonal)	1:400	1 Hour	Citrate	PROGEN Biotechnik	(Wagner et al. 2008)

IF, immunofluorescence; pSmad, phosphorylated small mothers against decapentaplegic; CTGF, connective tissue growth factor; SOSTDC1, sclerostin domain-containing-1; WT1, Wilms' tumor suppressor gene 1. Citrate: citrate buffer, pH 6.0, boiling for 15 min. EDTA: Tris-EDTA buffer, pH 9.0, boiling for 20 min.

∗h

5 conditions used for human tissue.

∗m

= conditions used for murine tissue.

Animal Experiments

Outbred male BALBc/129Sv CTGF^+/− mice, in which exon 1 of one CTGF allele had been replaced by a neomycin-resistant gene, were mated with female C57BL/6J mice. From the first offspring, female CTGF^+/− mice and female CTGF^+/+ littermates were used for this study. Diabetes was induced in five 16-week-old CTGF^+/− mice and four CTGF^+/+ mice by injection of streptozotocin. Nine control mice were injected with vehicle only. Mice were killed seventeen weeks after induction of diabetes (Nguyen et al. 2008a). The experiments were performed with the approval of the Experimental Animal Ethics Committee of the University of Utrecht.

Statistical Analysis

Data are presented as medians. Differences between control and diabetic subjects were calculated using the Mann-Whitney test. Association for WT1 and SOSTDC1 was calculated using linear regression. A p value of <0.05 was considered significant (two-tailed). The statistical analysis was performed using Graphpad Prism software for Windows, version 4.01 (GraphPad Software; San Diego, CA).

Results

Glomerular BMP Signaling Activity Is Decreased in Diabetic Nephropathy

Immunohistochemical nuclear staining of pSmad1/5/8 was much weaker in glomeruli of diabetic patients than in control kidneys (Figures 1A and 1B). The number of pSmad1/5/8-positive cells per glomerular cross section was clearly decreased in diabetes (9.2 versus 41.6 in controls, p<0.01; Figure 1C). Moreover, positive cells in diabetic glomeruli showed less-intense staining than those in control glomeruli (10.3 versus 23.6 arbitrary intensity units in controls, p<0.05; Figure 1G). In control glomeruli, pSmad1/5/8 was localized mainly in podocytes. Occasionally, weaker pSmad1/5/8 staining was observed in other cells, e.g., endothelial cells. In diabetic glomeruli, virtually no pSmad1/5/8 was seen, except in podocytes. The number of podocytes [as identified by nuclear Wilms' tumor suppressor (WT1) staining] per glomerular cross section was lower in diabetic subjects (14.3 versus 31.2 in controls, p<0.01; Figures 1D–1F). In consecutive sections stained for pSmad1/5/8 and WT1, glomeruli of control subjects contained more pSmad1/5/8-positive cells than WT1-positive podocytes. In contrast, diabetic glomeruli contained fewer pSmad1/5/8-positive cells than podocytes (Figure 1H).

Nephrin and Synaptopodin Are Decreased in Diabetic Nephropathy

Nephrin staining intensity showed a strong tendency (p = 0.056) toward decrease in diabetic glomeruli (Figures 2A and 2B), and the nephrin-positive area per glomerular tuft was decreased in diabetic kidneys (8.1% versus 21.6% in controls, p<0.01; Figure 2C).

Synaptopodin staining intensity showed a tendency (p = 0.095) toward decrease in diabetic glomeruli (Figures 2D and 2E). Furthermore, the synaptopodin-positive area per glomerular tuft was smaller in diabetic kidneys (13.1% versus 23.7% in controls, p<0.05; Figure 2F).

CTGF Is Upregulated, Whereas SOSTDC1 Is Decreased in Diabetic Nephropathy

In control glomeruli, CTGF expression was weak, whereas SOSTDC1 staining was very prominent. Double-immunofluorescent staining of CTGF and WT1 indicated that in control as well as diabetic glomeruli, CTGF is present only in podocytes (Figure 3A). CTGF was upregulated in diabetes, as evidenced by increased staining intensity and number of positive cells per glomerulus (11.1 versus 3.8 in controls, p<0.01; Figures 3B–3D).

The number of SOSTDC1-positive cells correlated with and was almost identical to WT1 counts, both in control and in diabetic glomeruli (R = 0.96, p<0.01; Figures 4A–4E). Moreover, double-immunofluorescent staining showed consistent colocalization of SOSTDC1 with synaptopodin (Figures 4F and 4G). Glomeruli of control kidneys showed hardly any variation in staining intensity. In contrast to CTGF, SOSTDC1 was decreased in diabetic glomeruli. This decrease of SOSTDC1 staining intensity varied between glomeruli, also within the same kidney, and paralleled the decrease of synaptopodin staining intensity (Figure 4H).

In Experimental Diabetic Nephropathy, CTGF Inhibits BMP Signaling

As shown previously, CTGF expression was increased in podocytes of diabetic wild-type (CTGF^+/+) mice, but not in diabetic CTGF^+/− mice (Nguyen et al. 2008a). Also, albuminuria was less pronounced in diabetic CTGF^+/− compared with diabetic wild-type mice (Nguyen et al. 2008a). To this we add that pSmad1/5/8 was mainly localized in podocytes. Consistent with the inhibitory effect of CTGF on BMP signaling, pSmad1/5/8 immunohistochemical staining was decreased only in diabetic wild-type mice, but preserved in diabetic CTGF^+/− mice (Figure 5).

Figure 1

Bone morphogenetic protein (BMP) signaling activity is decreased in human diabetic glomeruli. Nuclear staining of phosphorylated Smad1, −5, and −8 (pSmad1/5/8) in human non-diabetic control (CON) glomerulus (A) and diabetic (DN) glomerulus (B). Open arrows: pSmad1/5/8-positive podocytes. Closed arrow: pSmad1/5/8-positive endothelial cell. (D, E) Nuclear staining of the podocyte marker WT1 in control and diabetic subjects. (C) Quantification of pSmad1/5/8-positive cells in control and diabetic glomeruli. (F) Quantification of WT1-positive cells in control and diabetic glomeruli. (G) Mean intensity of pSmad1/5/8 staining per subject. (H) Correlation between WT1 and pSmad1/5/8 in consecutive sections of control as well as diabetic glomeruli. Open circles, control; closed circles, diabetic glomeruli. ∗p<0.05, ∗∗p<0.01. Bar = 50 μm.

Figure 2

Loss of podocyte differentiation markers in human diabetic glomeruli. Nephrin-positive area and staining intensity is reduced in diabetic (DN) as compared with control (CON) glomeruli (A, B). Similarly, synaptopodin-positive area and staining intensity is reduced in diabetic as compared with control glomeruli (D, E). (C) Quantification of nephrin-positive area per glomerular tuft. (F) Quantification of synaptopodin-positive area per glomerular tuft. Open circles, control; closed circles, diabetic glomeruli. ∗p<0.05, ∗∗p<0.01. Bar = 50 μm.

Figure 3

Connective tissue growth factor (CTGF) is upregulated in human diabetic glomeruli and localized in podocytes. (A) Double staining of CTGF and WT1 showed colocalization, indicating that CTGF is only present in podocytes. (B) Quantification of the number of CTGF-positive cells in control and diabetic glomeruli. Open circles, control; closed circles, diabetic glomeruli. (C, D) CTGF staining is both more intense and expressed in more cells in diabetic glomeruli (DN) compared with control glomeruli (CON). ∗∗p<0.01. Bar = 50 μm.

Discussion

The results of this study show that in human diabetic nephropathy, loss of podocytes and podocyte differentiation markers is associated with decreased BMP signaling activity, and that this might relate to increased CTGF expression. Strikingly, expression of SOSTDC1, another important antagonist of BMP signaling in the kidney, was found to be downregulated in diabetic glomeruli. In our specimens of diabetic nephropathy, the number of podocytes per glomerulus was significantly decreased, as evidenced by loss of WT1-positive nuclei. Similarly, the number of pSmad1/5/8-positive nuclei was decreased, indicating decreased BMP signaling activity. Also, the podocyte differentiation markers nephrin and synaptopodin were decreased in diabetic glomeruli. By immunohistochemistry, the two BMP antagonists known to be expressed in glomeruli, SOSTDC1 and CTGF, were found to be expressed primarily in normal and diabetic glomeruli, respectively. SOSTDC1, abundantly present in podocytes in control glomeruli, was downregulated in diabetic glomeruli, and therefore appears not to have a major role in decreased BMP signaling in diabetic nephropathy. CTGF, however, was hardly present in control glomeruli but strongly upregulated in podocytes in diabetic glomeruli. A possible role of CTGF in downregulation of BMP signaling in diabetic glomeruli was further emphasized by the preserved pSmad1/5/8 staining of podocyte nuclei that we observed in diabetic mice with hemizygous deletion of the CTGF gene (CTGF^+/− mice). Together, these data suggest that CTGF rather than SOSTDC1 contributes to loss of BMP signaling activity in diabetic nephropathy.

Figure 4

Sclerostin domain-containing-1 (SOSTDC1) is decreased in human diabetic glomeruli due to podocyte loss. (A–D) Representative staining of SOSTDC1 and WT1 in consecutive sections of control (CON) and diabetic (DN) glomeruli. (E) Correlation between WT1 and SOSTDC1 staining in consecutive sections of control (open circles) as well as diabetic glomeruli (closed circles). (F, G) SOSTDC1 expression is more pronounced in control glomeruli, and is limited to podocytes, as shown by co-localization with synaptopodin. (H) Congruent loss of SOSTDC1 and synaptopodin in glomeruli of a diabetic subject. Bar = 50 μm.

Decreased BMP signaling is an important determinant of adverse remodelling in renal response to injury, in particular diabetic nephropathy. BMP signaling activity is regulated at multiple levels. Major determinants include availability of various ligands and receptors, and extracellular modulators (Mitu and Hirschberg 2008). Phosphorylation of Smad1/5/8 is a central downstream element of BMP signal transduction, which makes it a good readout for this pathway. We show here that in human control glomeruli, pSmad1/5/8 is present mainly in podocytes. In diabetic glomeruli, we noticed a marked reduction of the number of pSmad1/5/8-positive cells. Not all of this reduction could be attributed to loss of podocytes. Control glomeruli contained more pSmad1/5/8-positive cells than podocytes. In contrast, in diabetic glomeruli, the number of podocytes exceeded that of pSmad1/5/8-positive cells. Moreover, the pSmad1/5/8 staining intensity was much lower in diabetic glomeruli.

Figure 5

CTGF contributes to loss of BMP signaling in experimental diabetic nephropathy. In control (CON) CTGF^+/− and CTGF^+/+ mice, pSmad1/5/8 staining in podocytes is comparable (A, C). Staining of pSmad1/5/8 is reduced in podocytes of diabetic (DN) wild-type mice (CTGF^+/+) (B), but preserved in diabetic mice with genetically impaired CTGF expression (CTGF^+/−) (D). Bar = 25 μm.

Both in vitro and in vivo studies have indicated that BMP-7 is important for maintenance of podocyte viability and differentiation (Wang et al. 2006; De Petris et al. 2007; Mitu et al. 2007). For example, in podocytes cultured under high glucose, Smad5 phosphorylation by BMP-7 led to increased podocyte survival, and BMP-7 treatment also restored synaptopodin and podocin expression (De Petris et al. 2007; Mitu et al. 2007). The loss of nephrin and synaptopodin we observed is consistent with previous studies of experimental and human diabetic nephropathy (Doublier et al. 2003; Benigni et al. 2004; Toyoda et al. 2004; Menne et al. 2006; Wang et al. 2006; De Petris et al. 2007; Wang et al. 2007). To this we add that in human diabetic nephropathy, loss of pSmad1/5/8 occurs in podocytes together with loss of the differentiation markers nephrin and synaptopodin, thus illustrating the relevance of the BMP signaling pathway in this disease.

There is growing evidence that several extracellular proteins, including SOSTDC1 and CTGF, can down-regulate BMP signaling activity in the kidney. SOSTDC1 is known to be expressed in tubuli and glomeruli of normal kidney (Blish et al. 2008). The role of SOSTDC1 in human tissues is largely unknown, but the observation that SOSTDC1 antagonized the Wnt pathway and that its expression was downregulated in renal cell carcinoma indicated strong antiproliferative activity of this protein (Blish et al. 2008). USAG-1, the rodent homolog of SOSTDC1, was first described as a negative regulator of the protective effects of BMP-7 in non-diabetic experimental nephropathies (Yanagita et al. 2006). Therefore, we postulated that SOSTDC1 might be up-regulated in human diabetic nephropathy, thus contributing to the decrease of glomerular pSmad1/5/8 activity. However, although the observed colocalization of SOSTDC1 with synaptopodin underscored the possible relevance of this BMP antagonist in podocyte biology, we observed a reduction of glomerular SOSTDC1 in human diabetic nephropathy. This suggests that in this disease, other factors might be more important in downregulation of BMP signaling activity.

We show that in glomeruli of human diabetic nephropathy, CTGF is upregulated and localized in podocytes, which is in accordance with previous reports (Wahab et al. 2005; Thomson et al. 2008). Although in this study, we found no clear evidence of CTGF staining in cells other than podocytes, we cannot exclude that CTGF is also present in, e.g., mesangial cells, as shown in some other studies (Ito et al. 1998; Rupérez et al. 2003; Wahab et al. 2005). Previous studies have shown that in both human and experimental diabetic nephropathy, glomerular CTGF is strongly upregulated and that plasma CTGF, as well as urine CTGF, might serve as a relevant biomarker in the progression of human diabetic nephropathy (Ito et al. 1998; Riser et al. 2000; Adler et al. 2001, 2002; Wahab et al. 2001; Nguyen et al. 2006, 2008b; Roestenberg et al. 2006; Guha et al. 2007; Yokoi et al. 2008). Exogenous recombinant human CTGF reduced pSmad1/5/8 level in the renal cortex, indicating that CTGF level significantly affects renal BMP signaling activity (Nguyen et al. 2008a). Moreover, inhibition of CTGF attenuated experimental diabetic nephropathy in at least three independent and fundamentally distinct studies involving neutralizing anti-CTGF antibodies, CTGF antisense oligonucleotides, and genetic deletion of one CTGF allele (CTGF^+/−) (Flyvbjerg et al. 2004; Guha et al. 2007; Nguyen et al. 2008a; Yokoi et al. 2008). In a previous study, we observed a decrease of pSmad1/5/8 abundance in diabetic CTGF^+/+ as compared with CTGF^+/− mice in Western blots of total renal cortex (Nguyen et al. 2008a). The observation in the present study that nuclear pSmad1/5/8 staining is preserved in podocytes of diabetic CTGF^+/− mice underscores the important role of CTGF in the loss of BMP signaling activity in the glomerulus. Apparently, the increase of BMP inhibition by CTGF exceeds the decrease of BMP inhibition by SOSTDC1.

We conclude that in addition to the previously observed downregulation of BMP-7 and BMP-receptor expression, overexpression of CTGF, rather than of SOSTDC1, might be an important determinant of loss of BMP signaling and of decreased podocyte number and differentiation in human diabetic nephropathy.

Footnotes

Acknowledgements

T.T. was supported by a European Renal Association–European Dialysis and Transplant Association research grant, J.W.L. was supported by a grant (C05.2144) from the Dutch Kidney Foundation, and T.Q.N. was supported by a Mozaïek grant (017.003.037) from the Dutch Organization for Scientific Research. S.V.T. was supported in part by Grant R21 CA-119181 from the National Institutes of Health and a gift from the Ben Mynatt family. R.G. has received research grants and consultancy fees from FibroGen, Inc.

The authors thank Dionne van der Giezen and Christine van Altena for technical assistance.

References

Adler

Kang

Feld

Cha

Barba

Striker

. (2001) Glomerular mRNAs in human type 1 diabetes: biochemical evidence for microalbuminuria as a manifestation of diabetic nephropathy. Kidney Int 60:2330–2336

Adler

Kang

Feld

Cha

Barba

Striker

. (2002) Can glomerular mRNAs in human type 1 diabetes be used to predict transition from normoalbuminuria to microalbuminuria? Am J Kidney Dis 40:184–188

Benigni

Gagliardini

Tomasoni

Abbate

Ruggenenti

Kalluri

Remuzzi

(2004) Selective impairment of gene expression and assembly of nephrin in human diabetic nephropathy. Kidney Int 65:2193–2200

Blish

Wang

Willingham

Birse

Krishnan

Brown

. (2008) A human bone morphogenetic protein antagonist is down-regulated in renal cancer. Mol Biol Cell 19:457–464

De Petris

Hruska

Chiechio

Liapis

(2007) Bone morphogenetic protein-7 delays podocyte injury due to high glucose. Nephrol Dial Transplant 22:3442–3450

Doublier

Salvidio

Lupia

Ruotsalainen

Verzola

Deferrari

Camussi

(2003) Nephrin expression is reduced in human diabetic nephropathy: evidence for a distinct role for glycated albumin and angiotensin II. Diabetes 52:1023–1030

Feng

Derynck

(2005) Specificity and versatility in tgf-beta signaling through Smads. Annu Rev Cell Dev Biol 21:659–693

Flyvbjerg

Khatir

Jensen

LJN

Lomongsod

Liu

Rasch

Usinger

(2004) Long-term renal effects of a neutralizing connective tissue growth factor (CTGF)-antibody in obese type 2 diabetic mice. J Am Soc Nephrol 15:261A

Guha

Tung

Lanting

Natarajan

(2007) Specific down-regulation of connective tissue growth factor attenuates progression of nephropathy in mouse models of type 1 and type 2 diabetes. FASEB J 21:3355–3368

10.

Ito

Aten

Bende

Oemar

Rabelink

Weening

Goldschmeding

(1998) Expression of connective tissue growth factor in human renal fibrosis. Kidney Int 53:853–861

11.

Menne

Meier

Park

Boehne

Kirsch

Lindschau

Ociepka

. (2006) Nephrin loss in experimental diabetic nephropathy is prevented by deletion of protein kinase C alpha signaling in-vivo. Kidney Int 70:1456–1462

12.

Mezzano

Droguett

Burgos

Aros

Ardiles

Flores

Carpio

. (2007) Expression of gremlin, a bone morphogenetic protein antagonist, in glomerular crescents of pauci-immune glomerulonephritis. Nephrol Dial Transplant 22:1882–1890

13.

Mitu

Hirschberg

(2008) Bone morphogenetic protein-7 (BMP7) in chronic kidney disease. Front Biosci 13:4726–4739

14.

Mitu

Wang

Hirschberg

(2007) BMP7 is a podocyte survival factor and rescues podocytes from diabetic injury. Am J Physiol Renal Physiol 293:F1641–F1648

15.

Nguyen

Goldschmeding

(2008) Bone morphogenetic protein-7 and connective tissue growth factor: novel targets for treatment of renal fibrosis? Pharm Res 25:2416–2426

16.

Nguyen

Roestenberg

van Nieuwenhoven

Bovenschen

Oliver

. (2008a) CTGF inhibits BMP-7 signaling in diabetic nephropathy. J Am Soc Nephrol 19:2098–2107

17.

Nguyen

Tarnow

Andersen

Hovind

Parving

Goldschmeding

van Nieuwenhoven

(2006) Urinary connective tissue growth factor excretion correlates with clinical markers of renal disease in a large population of type 1 diabetic patients with diabetic nephropathy. Diabetes Care 29:83–88

18.

Nguyen

Tarnow

Jorsal

Oliver

Roestenberg

Ito

Parving

. (2008b) Plasma connective tissue growth factor is an independent predictor of end-stage renal disease and mortality in type 1 diabetic nephropathy. Diabetes Care 31:1177–1182

19.

Riser

deNichilo

Cortes

Baker

Grondin

Yee

Narins

(2000) Regulation of connective tissue growth factor activity in cultured rat mesangial cells and its expression in experimental diabetic glomerulosclerosis. J Am Soc Nephrol 11:25–38

20.

Roestenberg

van Nieuwenhoven

Joles

Trischberger

Martens

Oliver

Aten

. (2006) Temporal expression profile and distribution pattern indicate a role of connective tissue growth factor (CTGF/CCN-2) in diabetic nephropathy in mice. Am J Physiol Renal Physiol 290:F1344–F1354

21.

Rupérez

Ruiz-Ortega

Esteban

Lorenzo

Mezzano

Plaza

Egido

(2003) Angiotensin II increases connective tissue growth factor in the kidney. Am J Pathol 163:1937–1947

22.

Shankland

(2006) The podocyte's response to injury: role in protein-uria and glomerulosclerosis. Kidney Int 69:2131–2147

23.

Thomson

McLennan

Kirwan

Heffernan

Hennessy

Yue

Twigg

(2008) Renal connective tissue growth factor correlates with glomerular basement membrane thickness and prospective albuminuria in a non-human primate model of diabetes: possible predictive marker for incipient diabetic nephropathy. J Diabetes Complications 22:284–294

24.

Toyoda

Suzuki

Umezono

Uehara

Maruyama

Honma

Sakai

. (2004) Expression of human nephrin mRNA in diabetic nephropathy. Nephrol Dial Transplant 19:380–385

25.

Wagner

Afanetti

Nevo

Antignac

Michiels

Schedl

. (2008) A novel Wilms' tumor 1 gene mutation in a child with severe renal dysfunction and persistent renal blastema. Pediatr Nephrol 23:1445–1453

26.

Wahab

Schaefer

Weston

Yiannikouris

Wright

Babelova

Schaefer

. (2005) Glomerular expression of thrombospondin-1, transforming growth factor beta and connective tissue growth factor at different stages of diabetic nephropathy and their interdependent roles in mesangial response to diabetic stimuli. Diabetologia 48:2650–2660

27.

Wahab

Yevdokimova

Weston

Roberts

Brinkman

Mason

(2001) Role of connective tissue growth factor in the pathogenesis of diabetic nephropathy. Biochem J 359:77–87

28.

Wang

Lai

Chow

Szeto

(2007) Messenger RNA expression of podocyte-associated molecules in the urinary sediment of patients with diabetic nephropathy. Nephron Clin Pract 106:c169–c179

29.

Wang

de Caestecker

Krishnan

Mitu

Lapage

Hirschberg

(2006) Renal bone morphogenetic protein-7 protects against diabetic nephropathy. J Am Soc Nephrol 17:2504–2512

30.

Yanagita

Okuda

Endo

Tanaka

Takahashi

Sugiyama

Kunita

. (2006) Uterine sensitization-associated gene-1 (USAG-1), a novel BMP antagonist expressed in the kidney, accelerates tubular injury. J Clin Invest 116:70–79

31.

Yokoi

Mukoyama

Mori

Kasahara

Suganami

Sawai

Yoshioka

. (2008) Overexpression of connective tissue growth factor in podocytes worsens diabetic nephropathy in mice. Kidney Int 73:446–455

BMP Signaling and Podocyte Markers are Decreased in Human Diabetic Nephropathy in Association with CTGF Overexpression

Abstract

Keywords

Materials and Methods

Human Tissue

Immunohistochemistry

Immunofluorescence

Quantification

Animal Experiments

Statistical Analysis

Results

Glomerular BMP Signaling Activity Is Decreased in Diabetic Nephropathy

Nephrin and Synaptopodin Are Decreased in Diabetic Nephropathy

CTGF Is Upregulated, Whereas SOSTDC1 Is Decreased in Diabetic Nephropathy

In Experimental Diabetic Nephropathy, CTGF Inhibits BMP Signaling

Discussion

Footnotes

Acknowledgements

References