TGFβ Regulation of Perilacunar/Canalicular Remodeling Is Sexually Dimorphic

Abstract

Bone fragility is the product of defects in bone mass and bone quality, both of which show sex-specific differences. Despite this, the cellular and molecular mechanisms underpinning the sexually dimorphic control of bone quality remain unclear, limiting our ability to effectively prevent fractures, especially in postmenopausal osteoporosis. Recently, using male mice, we found that systemic or osteocyte-intrinsic inhibition of TGFβ signaling, achieved using the 9.6-kb DMP1 promoter-driven Cre recombinase (TβRIIocy−/− mice), suppresses osteocyte perilacunar/canalicular remodeling (PLR) and compromises bone quality. Because systemic TGFβ inhibition more robustly increases bone mass in female than male mice, we postulated that sex-specific differences in bone quality could likewise result, in part, from dimorphic regulation of PLR by TGFβ. Moreover, because lactation induces PLR, we examined the effect of TGFβ inhibition on the female skeleton during lactation. In contrast to males, female mice that possess an osteocyte-intrinsic defect in TGFβ signaling were protected from TGFβ-dependent defects in PLR and bone quality. The expression of requisite PLR enzymes, the lacunocanalicular network (LCN), and the flexural strength of female TβRIIocy−/− bone was intact. With lactation, however, bone loss and induction in PLR and osteocytic parathyroid hormone type I receptor (PTHR1) expression, were suppressed in TβRIIocy−/− bone, relative to the control littermates. Indeed, differential control of PTHR1 expression, by TGFβ and other factors, may contribute to dimorphism in PLR regulation in male and female TβRIIocy−/− mice. These findings provide key insights into the sex-based differences in osteocyte PLR that underlie bone quality and highlight TGFβ signaling as a crucial regulator of lactation-induced PLR. © 2020 American Society for Bone and Mineral Research.

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 13, 2020
Source ID
10.1002/jbmr.4023

Entities

People

  • Claire Acevedo
  • Courtney M. Mazur
  • Cristal S. Yee
  • Neha S Dole
  • Tamara Alliston

Organizations

  • National Institute of Arthritis and Musculoskeletal and Skin Diseases
  • National Institute of Dental and Craniofacial Research
  • National Science Foundation
  • United States Department of Defense
  • University of California
  • University of Utah

Tags

Readers

  • Gender and Food Studies
  • Immunology and Pathology
  • Molecular Biology and Genetics