PLoS ONE · 2014 · 103 citations · 38 references
MedicineDevelopmental BiologyBone MetabolismCell SignalingStem Cell BiologyBone DevelopmentBone FormationBone HealingBone RegenerationOsteogenesisSkeletal DevelopmentBmp In Bone FormationBmp LigandsBmp Signal TransductionBmp-induced Cell DifferentiationFracture HealingOsteogenic DifferentiationOsteogenic Signaling PathwaysSmad Signaling Pathway
Platelet-derived growth factors (PDGFs) play important roles in skeletal development and bone fracture healing, yet how PDGFs execute their functions remains incompletely understood. Here we show that PDGF-AA, but not -AB or -BB, could activate the BMP-Smad1/5/8 pathway in mesenchymal stem cells (MSCs), which requires BMPRIA as well as PDGFRα. PDGF-AA promotes MSC osteogenic differentiation through the BMP-Smad1/5/8-Runx2/Osx axis and MSC migration via the BMP-Smad1/5/8-Twist1/Atf4 axis. Mechanistic studies show that PDGF-AA activates BMP-Smad1/5/8 signaling by feedback down-regulating PDGFRα, which frees BMPRI and allows for BMPRI-BMPRII complex formation to activate smad1/5/8, using BMP molecules in the microenvironment. This study unravels a physical and functional interaction between PDGFRα and BMPRI, which plays an important role in MSC differentiation and migration, and establishes a link between PDGF-AA and BMPs pathways, two essential regulators of embryonic development and tissue homeostasis.
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Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities.
Per Levéen, Milos Pekny, Samuel Gebré‐Medhin et al. · Genes & Development · 1994 · 1.1K citations · Full text