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Updated: May 18, 2026

Guided Differentiation of Mature Kidney Podocytes from Human Induced Pluripotent Stem Cells Under Chemically Defined Conditions
Published on: July 2, 2020
TGF-β/BMP pathways and the podocyte
Irini Tossidou1, Mario Schiffer
1Division of Nephrology, Hannover Medical School, Hannover, Germany.
Abstract:
Renal fibrosis is the major determinant in progression of acute and chronic kidney diseases. Transforming growth factor-β (TGF-β) has been shown to be an important mediator of progressive fibrosis. Several studies have implicated that TGF-β1 is involved in the tight balance of survival and apoptotic responses in podocytes that are Smad-dependent or independent. Bone morphogenic protein-7 (BMP-7), another member of the TGF-β superfamily, has to date been involved primarily in kidney development and was described as an active blocker of TGF-β-induced profibrotic effects. Here, we summarize the direct effects of these two cytokines on podocytes. We describe their involvement in podocyte survival and apoptosis pathways with the potential to modify the critical steps in podocyte apoptosis induction. Our group has analyzed the cross-talk of BMP-7 and TGF-β1 signaling in podocytes and we describe BMP-7 as a cytoprotective factor that could antagonize proapoptotic TGF-β signals. In addition, we identified various extracellular and intracellular modifiers that can influence this sensitive cross-talk. On the basis of our work and the work of others we conclude that the balance of TGF-β1 and BMP-7 signaling and involvement of extracellular and intracellular modifiers in these cascades are important parts of podocyte physiology and pathophysiology.
Insights
Transforming growth factor-β1 (TGF-β1) promotes kidney fibrosis, while Bone morphogenic protein-7 (BMP-7) protects podocytes. BMP-7 antagonizes TGF-β1
Area of Science:
- Nephrology
- Molecular Biology
- Cell Biology
Background:
- Renal fibrosis is a key factor in kidney disease progression.
- Transforming growth factor-β (TGF-β) signaling, particularly TGF-β1, mediates fibrosis.
- Podocyte apoptosis is a critical step in kidney disease pathogenesis.
Purpose of the Study:
- To summarize the direct effects of TGF-β1 and Bone morphogenic protein-7 (BMP-7) on podocytes.
- To describe their roles in podocyte survival and apoptosis pathways.
- To analyze the cross-talk between BMP-7 and TGF-β1 signaling in podocytes.
Main Methods:
- Review of existing literature on TGF-β1 and BMP-7 effects on podocytes.
- Analysis of signaling pathways involved in podocyte apoptosis.
- Investigation of the interplay between BMP-7 and TGF-β1 in podocyte cultures.
Main Results:
- BMP-7 acts as a cytoprotective factor in podocytes.
- BMP-7 antagonizes pro-apoptotic TGF-β1 signals.
- Extracellular and intracellular modifiers influence the BMP-7/TGF-β1 signaling cross-talk.
Conclusions:
- The balance between TGF-β1 and BMP-7 signaling is crucial for podocyte physiology.
- Modulators of this signaling balance are important in kidney pathophysiology.
- BMP-7 holds potential as a therapeutic agent against kidney fibrosis.
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