Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.

Bone continually adapts to meet changing physical and biological demands. Osteoblasts, osteoclasts, and osteocytes cooperate to integrate these physical and biochemical cues to maintain bone homeostasis. Although TGFβ acts on all three of these cell types to maintain bone homeostasis, the extent to...

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Main Authors: Jacqueline Nguyen, Simon Y Tang, Daniel Nguyen, Tamara Alliston
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3538690?pdf=render
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author Jacqueline Nguyen
Simon Y Tang
Daniel Nguyen
Tamara Alliston
author_facet Jacqueline Nguyen
Simon Y Tang
Daniel Nguyen
Tamara Alliston
author_sort Jacqueline Nguyen
collection DOAJ
description Bone continually adapts to meet changing physical and biological demands. Osteoblasts, osteoclasts, and osteocytes cooperate to integrate these physical and biochemical cues to maintain bone homeostasis. Although TGFβ acts on all three of these cell types to maintain bone homeostasis, the extent to which it participates in the adaptation of bone to mechanical load is unknown. Here, we investigated the role of the TGFβ pathway in load-induced bone formation and the regulation of Sclerostin, a mechanosensitive antagonist of bone anabolism. We found that mechanical load rapidly represses the net activity of the TGFβ pathway in osteocytes, resulting in reduced phosphorylation and activity of key downstream effectors, Smad2 and Smad3. Loss of TGFβ sensitivity compromises the anabolic response of bone to mechanical load, demonstrating that the mechanosensitive regulation of TGFβ signaling is essential for load-induced bone formation. Furthermore, sensitivity to TGFβ is required for the mechanosensitive regulation of Sclerostin, which is induced by TGFβ in a Smad3-dependent manner. Together, our results show that physical cues maintain bone homeostasis through the TGFβ pathway to regulate Sclerostin expression and the deposition of new bone.
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spelling doaj.art-7fef5159d71a47c6ba2df220dc830e392022-12-22T00:03:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5381310.1371/journal.pone.0053813Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.Jacqueline NguyenSimon Y TangDaniel NguyenTamara AllistonBone continually adapts to meet changing physical and biological demands. Osteoblasts, osteoclasts, and osteocytes cooperate to integrate these physical and biochemical cues to maintain bone homeostasis. Although TGFβ acts on all three of these cell types to maintain bone homeostasis, the extent to which it participates in the adaptation of bone to mechanical load is unknown. Here, we investigated the role of the TGFβ pathway in load-induced bone formation and the regulation of Sclerostin, a mechanosensitive antagonist of bone anabolism. We found that mechanical load rapidly represses the net activity of the TGFβ pathway in osteocytes, resulting in reduced phosphorylation and activity of key downstream effectors, Smad2 and Smad3. Loss of TGFβ sensitivity compromises the anabolic response of bone to mechanical load, demonstrating that the mechanosensitive regulation of TGFβ signaling is essential for load-induced bone formation. Furthermore, sensitivity to TGFβ is required for the mechanosensitive regulation of Sclerostin, which is induced by TGFβ in a Smad3-dependent manner. Together, our results show that physical cues maintain bone homeostasis through the TGFβ pathway to regulate Sclerostin expression and the deposition of new bone.http://europepmc.org/articles/PMC3538690?pdf=render
spellingShingle Jacqueline Nguyen
Simon Y Tang
Daniel Nguyen
Tamara Alliston
Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
PLoS ONE
title Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
title_full Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
title_fullStr Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
title_full_unstemmed Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
title_short Load regulates bone formation and Sclerostin expression through a TGFβ-dependent mechanism.
title_sort load regulates bone formation and sclerostin expression through a tgfβ dependent mechanism
url http://europepmc.org/articles/PMC3538690?pdf=render
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AT simonytang loadregulatesboneformationandsclerostinexpressionthroughatgfbdependentmechanism
AT danielnguyen loadregulatesboneformationandsclerostinexpressionthroughatgfbdependentmechanism
AT tamaraalliston loadregulatesboneformationandsclerostinexpressionthroughatgfbdependentmechanism