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CTGF inhibits BMP-7 signaling in diabetic nephropathy
Tri Q Nguyen1, Peggy Roestenberg, Frans A van Nieuwenhoven
1Department of Pathology, University Medical Center Utrecht, H04.312, Heidelberglaan 100, 3584 CX, Utrecht, Netherlands.
Abstract:
In diabetic nephropathy, connective tissue growth factor (CTGF) is upregulated and bone morphogenetic protein 7 (BMP-7) is downregulated. CTGF is known to inhibit BMP-4, but similar cross-talk between BMP-7 and CTGF has not been studied. In this study, it was hypothesized that CTGF acts as an inhibitor of BMP-7 signaling activity in diabetic nephropathy. Compared with diabetic wild-type CTGF(+/+) mice, diabetic CTGF(+/-) mice had approximately 50% lower CTGF mRNA and protein, less severe albuminuria, no thickening of the glomerular basement membrane, and preserved matrix metalloproteinase (MMP) activity. Although the amount of BMP-7 mRNA was similar in the kidneys of diabetic CTGF(+/+) and CTGF(+/-) mice, phosphorylation of the BMP signal transduction protein Smad1/5 and expression of the BMP target gene Id1 were lower in diabetic CTGF(+/+) mice. Moreover, renal Id1 mRNA expression correlated with albuminuria (R = -0.86) and MMP activity (R = 0.76). In normoglycemic mice, intraperitoneal injection of CTGF led to a decrease of pSmad1/5 in the renal cortex. In cultured renal glomerular and tubulointerstitial cells, CTGF diminished BMP-7 signaling activity, evidenced by lower levels of pSmad1/5, Id1 mRNA, and BMP-responsive element-luciferase activity. Co-immunoprecipitation, solid-phase binding assay, and surface plasmon resonance analysis showed that CTGF binds BMP-7 with high affinity (Kd approximately 14 nM). In conclusion, upregulation of CTGF inhibits BMP-7 signal transduction in the diabetic kidney and contributes to altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria, all of which are hallmarks of diabetic nephropathy.
Insights
Connective tissue growth factor (CTGF) inhibits bone morphogenetic protein 7 (BMP-7) signaling in diabetic nephropathy, worsening kidney damage. Reducing CTGF levels in mice improved kidney function and reduced disease markers.
Area of Science:
- Nephrology
- Molecular Biology
- Biochemistry
Background:
- Diabetic nephropathy is characterized by increased connective tissue growth factor (CTGF) and decreased bone morphogenetic protein 7 (BMP-7).
- The interaction between CTGF and BMP-7 signaling in diabetic kidney disease remains uncharacterized.
Purpose of the Study:
- To investigate the hypothesis that CTGF inhibits BMP-7 signaling activity in the context of diabetic nephropathy.
- To elucidate the molecular mechanisms underlying CTGF's role in diabetic kidney disease progression.
Main Methods:
- Comparison of diabetic wild-type and CTGF(+/-) mice to assess kidney function and molecular markers.
- In vivo studies involving CTGF administration in normoglycemic mice.
- In vitro experiments using cultured renal cells to evaluate BMP-7 signaling.
- Biochemical assays including co-immunoprecipitation and surface plasmon resonance to determine CTGF-BMP-7 binding.
Main Results:
- Diabetic CTGF(+/-) mice exhibited reduced albuminuria, preserved glomerular basement membrane, and maintained matrix metalloproteinase (MMP) activity compared to wild-type.
- CTGF administration decreased BMP-7 signaling, evidenced by reduced Smad1/5 phosphorylation and Id1 expression in kidneys and cultured cells.
- CTGF directly binds to BMP-7 with high affinity (Kd ≈ 14 nM).
Conclusions:
- Upregulated CTGF in diabetic nephropathy inhibits BMP-7 signal transduction.
- This inhibition contributes to key pathological features including altered gene transcription, reduced MMP activity, glomerular basement membrane thickening, and albuminuria.
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