Blockade of receptor-activated G(i) signaling in osteoblasts in vivo leads to site-specific increases in cortical and cancellous bone formation

Millard, Susan .M, Louie, Alyssa M., Wattanachanya, Lalita, Wronski, Thomas J., Conklin, Bruce R. and Nissenson, Robert A. (2011) Blockade of receptor-activated G(i) signaling in osteoblasts in vivo leads to site-specific increases in cortical and cancellous bone formation. Journal of Bone and Mineral Research, 26 4: 822-832. doi:10.1002/jbmr.273


Author Millard, Susan .M
Louie, Alyssa M.
Wattanachanya, Lalita
Wronski, Thomas J.
Conklin, Bruce R.
Nissenson, Robert A.
Title Blockade of receptor-activated G(i) signaling in osteoblasts in vivo leads to site-specific increases in cortical and cancellous bone formation
Formatted title
Blockade of receptor-activated Gi signaling in osteoblasts in vivo leads to site-specific increases in cortical and cancellous bone formation
Journal name Journal of Bone and Mineral Research   Check publisher's open access policy
ISSN 0884-0431
1523-4681
Publication date 2011-04-01
Sub-type Article (original research)
DOI 10.1002/jbmr.273
Volume 26
Issue 4
Start page 822
End page 832
Total pages 11
Place of publication Malden, MA,United States
Publisher Wiley-Blackwell Publishing
Collection year 2012
Language eng
Formatted abstract
Osteoblasts play a critical role in the maintenance of bone mass through bone formation and regulation of bone resorption. Targeted expression of a constitutively active engineered Gi-coupled G protein–coupled receptor (GPCR) to osteoblasts in vivo leads to severe osteopenia. However, little is known about the role of endogenous receptor-mediated Gi signaling in regulating osteoblast function.In this study, we investigated the skeletal effects of blocking Gi-coupled signaling in osteoblasts in vivo. This was accomplished by transgenic expression of the catalytic subunit of pertussis toxin (PTX) under control of the collagen Iα 2.3-kb promoter. These mice, designated Col1(2.3)+/PTX+, showed increased cortical thickness at the femoral midshaft at 12 weeks of age. This correlated with increased periosteal bone formation associated with expanded mineralizing surface observed in 8-week-old mice of both genders. The cancellous bone phenotype of the Col1(2.3)+/PTX+ mice was sexually dimorphic, with increases in fractional bone volume at the distal femur seen only in females. Similarly, while cancellous bone-formation rates were unchanged in males, they could not be quantified for female Col1(2.3)+/PTX+ mice owing to the disorganized nature of the labeling pattern, which was consistent with rapid formation of woven bone. Alterations in osteoclast activity did not appear to participate in the phenotype. These data demonstrate that Gi-coupled signaling by GPCRs endogenous to osteoblasts plays a complex role in the regulation of bone formation in a manner that is dependent on both gender and the anatomic site within bone.
Keyword Osteoblasts
G Protein-Coupled Receptors
G(i) Signaling
Periosteal Bone Formation
Sexual Dimorphism
Inbred Mice
Q-Index Code C1
Q-Index Status Confirmed Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: UQ Centre for Clinical Research Publications
Non HERDC
 
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