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Mol Cell Biol. 2017 Feb 1;37(4). pii: e00253-16. doi: 10.1128/MCB.00253-16. Print 2017 Feb 15.

Bmp Induces Osteoblast Differentiation through both Smad4 and mTORC1 Signaling.

Author information

1
Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
2
Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, Missouri, USA flong@wustl.edu.
3
Department of Developmental Biology, Washington University School of Medicine, St. Louis, Missouri, USA.

Abstract

The bone morphogenetic protein (Bmp) family of secreted molecules has been extensively studied in the context of osteoblast differentiation. However, the intracellular signaling cascades that mediate the osteoblastogenic function of Bmp have not been fully elucidated. By profiling mRNA expression in the bone marrow mesenchymal progenitor cell line ST2, we discover that BMP2 induces not only genes commonly associated with ossification and mineralization but also genes important for general protein synthesis. We define the two groups of genes as mineralization related versus protein anabolism signatures of osteoblasts. Although it induces the expression of several Wnt genes, BMP2 activates the osteogenic program largely independently of de novo Wnt secretion. Remarkably, although Smad4 is necessary for the activation of the mineralization-related genes, it is dispensable for BMP2 to induce the protein anabolism signature, which instead critically depends on the transcription factor Atf4. Upstream of Atf4, BMP2 activates mTORC1 to stimulate protein synthesis, resulting in an endoplasmic reticulum stress response mediated by Perk. Thus, Bmp signaling induces osteoblast differentiation through both Smad4- and mTORC1-dependent mechanisms.

KEYWORDS:

Atf4; ER stress; Perk; Smad4; bone morphogenic proteins (BMPs); mTOR; mTORC1; mineralization; osteoblast; protein anabolism

PMID:
27920253
PMCID:
PMC5288572
DOI:
10.1128/MCB.00253-16
[Indexed for MEDLINE]
Free PMC Article

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