The integrity of the adult skeleton undergoes constant and dynamic remodeling to maintain bone homeostasis, which is achieved by the tight control of coupling between osteoclast-mediated bone resorption and osteoblast-mediated bone formation. However, the balance of this bone remodeling process is disrupted in pathological conditions. Chronic inflammation is one of the most evident and common pathological settings that often lead to deregulated bone remodeling characterized by excessive bone loss but limited bone formation, such as occurs in rheumatoid arthritis (RA), periodontitis and peri- prosthetic loosening. The disturbances in bone remodeling in these diseases are refractory to current antiresorptive treatments and lead to continuous musculoskeletal tissue damage and accelerating pathogenesis. The mechanisms that impact the deregulated bone remodeling in pathological conditions are largely unknown, which is a barrier to successfully treating the numerous diseases associated with bone loss. Our long term goals are to identify and understand the mechanisms that regulate bone remodeling in inflammatory settings, and to utilize this knowledge in development of new therapeutic approaches to diseases associated with inflammatory osteolysis. We are particularly interested in TNF- ??mediated bone remodeling since TNF-? is a key pathogenic factor driving inflammatory bone resorption. We have recently identified Def6 that functions as a novel regulator of bone remodeling in both physiological conditions and TNF-?-mediated inflammatory settings. Def6 suppresses osteoclast differentiation while enhancing osteoblast differentiation in response to TNF-? stimulation. Importantly, Def6 expression levels are downregulated by TNF-? and inversely correlate with TNF-? levels in RA patients, indicating a potentially important role of Def6 in the pathogenesis of deregulated bone remodeling in RA. In this application, we will apply genetic approaches and use both in vitro cell culture systems and arthritis animal models to investigate: 1) the mechanisms by which Def6 regulates bone remodeling factors, with a focus on the epigenetic regulation of DKK1 expression and the DKK1-Wnt mediated remodeling axis by Def6; 2) the mechanisms by which Def6 regulates both osteoclast and osteoblast differentiation; and 3) the functional importance of Def6 in inflammatory arthritic bone resorption using both loss and gain of function of Def6 in inflammatory arthritis animal models. A structure-function analysis of Def6 will be performed to identify the domain(s) and/or phosphorylation site(s) that are important for Def6 function in bone remodeling. We anticipate that our studies will yield insight into mechanisms that restrain inflammatory osteolysis, and will be useful in developing new therapeutic approaches to suppressing bone resorption in inflammatory settings.

Public Health Relevance

Bone erosion is a severe consequence of inflammatory diseases associated with bone loss, such as rheumatoid arthritis. This application will explore mechanisms that inhibit bone erosion while promoting bone repair, thereby providing new attractive therapeutic approaches to suppressing inflammatory bone erosion and preventing disease development and progress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR068970-03
Application #
9627926
Study Section
Skeletal Biology Development and Disease Study Section (SBDD)
Program Officer
Chen, Faye H
Project Start
2016-04-01
Project End
2022-01-31
Budget Start
2019-02-01
Budget End
2020-01-31
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Hospital for Special Surgery
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10021
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Zhao, Baohong (2017) TNF and Bone Remodeling. Curr Osteoporos Rep 15:126-134
Shang, Yingli; Coppo, Maddalena; He, Teng et al. (2016) The transcriptional repressor Hes1 attenuates inflammation by regulating transcription elongation. Nat Immunol 17:930-7
Fang, Celestia; Qiao, Yu; Mun, Se Hwan et al. (2016) Cutting Edge: EZH2 Promotes Osteoclastogenesis by Epigenetic Silencing of the Negative Regulator IRF8. J Immunol 196:4452-4456
Miller, Christine H; Smith, Sinead M; Elguindy, Mahmoud et al. (2016) RBP-J-Regulated miR-182 Promotes TNF-?-Induced Osteoclastogenesis. J Immunol 196:4977-86