Emerging role of senescent microglia in brain aging-related neurodegenerative diseases.
Chan RimMin-Jung YouMinyeop NahmMin-Soo KwonPublished in: Translational neurodegeneration (2024)
Brain aging is a recognized risk factor for neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease), but the intricate interplay between brain aging and the pathogenesis of these conditions remains inadequately understood. Cellular senescence is considered to contribute to cellular dysfunction and inflammaging. According to the threshold theory of senescent cell accumulation, the vulnerability to neurodegenerative diseases is associated with the rates of senescent cell generation and clearance within the brain. Given the role of microglia in eliminating senescent cells, the accumulation of senescent microglia may lead to the acceleration of brain aging, contributing to inflammaging and increased vulnerability to neurodegenerative diseases. In this review, we propose the idea that the senescence of microglia, which is notably vulnerable to aging, could potentially serve as a central catalyst in the progression of neurodegenerative diseases. The senescent microglia are emerging as a promising target for mitigating neurodegenerative diseases.
Keyphrases
- resting state
- white matter
- inflammatory response
- amyotrophic lateral sclerosis
- neuropathic pain
- functional connectivity
- single cell
- climate change
- endothelial cells
- dna damage
- multiple sclerosis
- induced apoptosis
- oxidative stress
- stem cells
- spinal cord
- spinal cord injury
- cognitive decline
- mesenchymal stem cells
- room temperature
- mild cognitive impairment
- signaling pathway
- gold nanoparticles
- brain injury
- bone marrow