Osteoarthritis is classically defined as a non-inflammatory arthritis caused by excessive mechanical loading on the joint/cartilage. Osteoarthritis is also linked to obesity, which is commonly attributed to increased joint load caused by body weight. Multiple lines of evidence suggest that, in addition to mechanical loading, there are non-mechanical contributors to the development of osteoarthritis. Low-grade chronic systemic inflammation, associated with obesity and the metabolic syndrome, has been implicated as a non-mechanical contributor to osteoarthritis. However, the co-occurrence of obesity and systemic inflammation in most animal models and patients has so far made it difficult to separate the effects of the two factors on osteoarthritis. The proposed Exploratory/Developmental Research project is based on the hypothesis that low-grade chronic systemic inflammation originating in the gut enhances the adverse effects of mechanical load on the development of osteoarthritis. We propose separating the effects of systemic inflammation from obesity using the TLR5 deficient mouse, which spontaneously develops gut flora dysbiosis leading to gut inflammation, low-grade chronic systemic inflammation and a metabolic syndrome-like phenotype. Using a load-induced osteoarthritis model and the fact that inflammation in the TLR5 deficient mouse originates in the gut rather than from obesity, the project includes one aim: to determine the relationship between applied load magnitude and development of osteoarthritis in the TLR5 deficient mouse under three conditions: mild inflammation/mild increased body weight (natural state), mild inflammation/normal body weight (limit fed), and normal inflammation/normal body weight (antibiotic treated). Our findings will tes the idea that systemic inflammation influences susceptibility to osteoarthritis even in the absence of obesity and has the potential to provide the first evidence that changes in gut microbiota (the upstream cause of the TLR5KO phenotype) can influence susceptibility to osteoarthritis.

Public Health Relevance

Osteoarthritis is a debilitating disease that is linked to obesity and a state of chronic systemic inflammation. In this project we test the idea that systemic inflammation can influence the susceptibility to osteoarthritis in situations where obesity is absent. The proposed work has the potential to lead to new methods of preventing or impairing the progression of osteoarthritis by regulating systemic inflammation, potentially through regulation of the gut microbiome.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AR068061-02
Application #
9015411
Study Section
Skeletal Biology Structure and Regeneration Study Section (SBSR)
Program Officer
Tyree, Bernadette
Project Start
2015-03-01
Project End
2016-12-31
Budget Start
2016-01-01
Budget End
2016-12-31
Support Year
2
Fiscal Year
2016
Total Cost
$150,911
Indirect Cost
$51,911
Name
Cornell University
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Guss, Jason D; Horsfield, Michael W; Fontenele, Fernanda F et al. (2017) Alterations to the Gut Microbiome Impair Bone Strength and Tissue Material Properties. J Bone Miner Res 32:1343-1353
Hernandez, Christopher J (2017) The Microbiome and Bone and Joint Disease. Curr Rheumatol Rep 19:77
Hernandez, Christopher J; van der Meulen, Marjolein Ch (2017) Understanding Bone Strength Is Not Enough. J Bone Miner Res 32:1157-1162
Hernandez, Christopher J; Guss, Jason D; Luna, Marysol et al. (2016) Links Between the Microbiome and Bone. J Bone Miner Res 31:1638-46