Lessons from Microglia Aging for the Link between Inflammatory Bone Disorders and Alzheimer's Disease.
Zhou WuHiroshi NakanishiPublished in: Journal of immunology research (2015)
Bone is sensitive to overactive immune responses, which initiate the onset of inflammatory bone disorders, such as rheumatoid arthritis and periodontitis, resulting in a significant systemic inflammatory response. On the other hand, neuroinflammation is strongly implicated in Alzheimer's disease (AD), which can be enhanced by systemic inflammation, such as that due to cardiovascular disease and diabetes. There is growing clinical evidence supporting the concept that rheumatoid arthritis and periodontitis are positively linked to AD, suggesting that inflammatory bone disorders are risk factors for this condition. Recent studies have suggested that leptomeningeal cells play an important role in transducing systemic inflammatory signals to brain-resident microglia. More importantly, senescent-type, but not juvenile-type, microglia provoke neuroinflammation in response to systemic inflammation. Because the prevalence of rheumatoid arthritis and periodontitis increases with age, inflammatory bone disorders may be significant sources of covert systemic inflammation among elderly people. The present review article highlights our current understanding of the link between inflammatory bone disorders and AD with a special focus on microglia aging.
Keyphrases
- inflammatory response
- rheumatoid arthritis
- bone mineral density
- cardiovascular disease
- oxidative stress
- lipopolysaccharide induced
- bone loss
- soft tissue
- type diabetes
- lps induced
- bone regeneration
- immune response
- postmenopausal women
- disease activity
- traumatic brain injury
- induced apoptosis
- toll like receptor
- risk factors
- metabolic syndrome
- interstitial lung disease
- cell death
- cell proliferation
- signaling pathway
- systemic lupus erythematosus
- white matter
- idiopathic pulmonary fibrosis
- skeletal muscle
- cardiovascular risk factors
- cell cycle arrest
- multiple sclerosis