Cells in the osteoblast lineage are crucial for controlling bone formation and bone resorption throughout life. An in-depth understanding of how signaling processes within osteoblast-lineage cells are linked to bone formation and bone resorption is essential to provide new insights into skeletal physiology and to open up new avenues for osteoporosis therapy. In this regard, the G protein signaling pathway is crucial in that the only FDA-approved anabolic treatment for osteoporosis is intermittent parathyroid hormone which activates two G proteins- Gs and Gq- through a G protein coupled receptor (GPCR) in osteoblasts. Previous studies have focused largely on the role of Gs signaling, and little is known about the function of other osteoblast G protein pathways such as Gi and Gq. It is vital that we increase our understanding of how specific G protein signals in osteoblasts are linked to bone formation and bone resorption, and to define their pathophysiological significance. The complexity of the skeletal environment required for normal bone formation and turnover make it necessary to use in vivo models to address these critical issues. Our laboratory has established the utility of an approach to dissect the role of specific signaling pathways using transgenic mice expressing engineered GPCRs termed RASSLs (Receptors Activated Solely by Synthetic Ligands). Our results so far demonstrate that activation of the Gs signaling pathway in mature osteoblasts results in a massive increase in the formation of trabecular bone with a marked reduction in marrow elements and erosion of the cortex. By contract, activation of the Gi signaling pathway in mature osteoblasts results in trabecular osteopenia due to decreased rates of bone formation. Recently, we have developed a method to block endogenous Gi signaling in osteoblasts in vivo using the targeted expression of the catalytic subunit of pertussis toxin. In female mice, blockade of osteoblast Gi signaling results in increased trabecular bone formation during bone growth, and completely prevents age-related trabecular bone loss. These exciting findings indicate that endogenous Gi signaling in osteoblasts negatively regulates bone formation, and suggest that this pathway is an important contributor to age-related bone loss. In the present proposal, we will extend these observations and probe their pathophysiological relevance. Specifically, we will: 1) determine the pathophysiological importance of osteoblast Gi signaling in age-related bone loss, and assess whether osteoblast Gi signaling limits the effectiveness of PTH as an anabolic agent;2) identify the mechanisms whereby osteoblast Gi signaling negatively regulates bone formation;and 3) determine the role of Gq signaling in mature OBs in regulating skeletal homeostasis. The knowledge gained from these studies will provide new insights into the control of osteoblastic bone formation, and these will be valuable in the design and development of improved anabolic therapies for osteoporosis.

Public Health Relevance

Osteoporosis is a major loss of bone mass and strength due to the failure of bone formation to keep up with bone resorption. In occurs in both men and women with advancing age. In addition to age, risk factors for the development of osteoporosis include immobility, glucocorticoid therapy, alcoholism, and smoking. Thus, the veteran population is at high risk for the development of osteoporosis. The present studies are designed to define the mechanisms that control normal bone formation and that are necessary and sufficient for anabolic responses. This knowledge can be exploited for the development of targeted therapeutics to stimulate bone formation in patients with osteoporosis.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
5I01BX001496-02
Application #
8413401
Study Section
Endocrinology B (ENDB)
Project Start
2011-10-01
Project End
2015-09-30
Budget Start
2012-10-01
Budget End
2013-09-30
Support Year
2
Fiscal Year
2013
Total Cost
Indirect Cost
Name
Veterans Affairs Medical Center San Francisco
Department
Type
DUNS #
078763885
City
San Francisco
State
CA
Country
United States
Zip Code
94121
Wang, Liping; Roth, Theresa; Abbott, Marcia et al. (2017) Osteoblast-derived FGF9 regulates skeletal homeostasis. Bone 98:18-25
Millard, Susan M; Wang, Liping; Wattanachanya, Lalita et al. (2017) Role of Osteoblast Gi Signaling in Age-Related Bone Loss in Female Mice. Endocrinology 158:1715-1726
Wang, Liping; Carroll, Dylan O'; Liu, Xuhui et al. (2015) Effects of blockade of endogenous Gi signaling in Tie2-expressing cells on bone formation in a mouse model of heterotopic ossification. J Orthop Res 33:1212-7
Wattanachanya, Lalita; Wang, Liping; Millard, Susan M et al. (2015) Assessing the osteoblast transcriptome in a model of enhanced bone formation due to constitutive Gs-G protein signaling in osteoblasts. Exp Cell Res 333:289-302
Kang, Heejae; Dang, Alexis B C; Joshi, Sunil K et al. (2014) Novel mouse model of spinal cord injury-induced heterotopic ossification. J Rehabil Res Dev 51:1109-18
Liu, Xuhui; Kang, Heejae; Shahnazari, Mohammad et al. (2014) A novel mouse model of trauma induced heterotopic ossification. J Orthop Res 32:183-8
Shahnazari, Mohammad; Chu, Vivian; Wronski, Thomas J et al. (2013) CXCL12/CXCR4 signaling in the osteoblast regulates the mesenchymal stem cell and osteoclast lineage populations. FASEB J 27:3505-13
Wattanachanya, Lalita; Lu, Wei-Dar; Kundu, Ramendra K et al. (2013) Increased bone mass in mice lacking the adipokine apelin. Endocrinology 154:2069-80
Kao, Richard S; Abbott, Marcia J; Louie, Alyssa et al. (2013) Constitutive protein kinase A activity in osteocytes and late osteoblasts produces an anabolic effect on bone. Bone 55:277-87
Kao, Richard; Lu, Weidar; Louie, Alyssa et al. (2012) Cyclic AMP signaling in bone marrow stromal cells has reciprocal effects on the ability of mesenchymal stem cells to differentiate into mature osteoblasts versus mature adipocytes. Endocrine 42:622-36

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