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Osteocyte-Intrinsic TGF-β Signaling Regulates Bone Quality through Perilacunar/Canalicular Remodeling
Author(s) -
Neha S. Dole,
Courtney M. Mazur,
Claire Acevedo,
Justin P. Lopez,
David A. Monteiro,
Tristan W. Fowler,
Bernd Gludovatz,
Flynn Walsh,
Jen. Regan,
Sara A. Messina,
Daniel S. Evans,
Thomas Lang,
Bin Zhang,
Robert O. Ritchie,
Khalid S. Mohammad,
Tamara Alliston
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.10.115
Subject(s) - osteocyte , microbiology and biotechnology , bone remodeling , transforming growth factor , signal transduction , chemistry , biology , endocrinology , osteoblast , biochemistry , in vitro
Poor bone quality contributes to bone fragility in diabetes, aging, and osteogenesis imperfecta. However, the mechanisms controlling bone quality are not well understood, contributing to the current lack of strategies to diagnose or treat bone quality deficits. Transforming growth factor beta (TGF-β) signaling is a crucial mechanism known to regulate the material quality of bone, but its cellular target in this regulation is unknown. Studies showing that osteocytes directly remodel their perilacunar/canalicular matrix led us to hypothesize that TGF-β controls bone quality through perilacunar/canalicular remodeling (PLR). Using inhibitors and mice with an osteocyte-intrinsic defect in TGF-β signaling (TβRII ocy-/- ), we show that TGF-β regulates PLR in a cell-intrinsic manner to control bone quality. Altogether, this study emphasizes that osteocytes are key in executing the biological control of bone quality through PLR, thereby highlighting the fundamental role of osteocyte-mediated PLR in bone homeostasis and fragility.

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