NRF2 Activation and Downstream Effects: Focus on Parkinson's Disease and Brain Angiotensin.
Juan A PargaAna Isabel Rodriguez-PerezMaria Garcia-GarroteJannette Rodriguez-PallaresJose Luis Labandeira-GarciaPublished in: Antioxidants (Basel, Switzerland) (2021)
Reactive oxygen species (ROS) are signalling molecules used to regulate cellular metabolism and homeostasis. However, excessive ROS production causes oxidative stress, one of the main mechanisms associated with the origin and progression of neurodegenerative disorders such as Parkinson's disease. NRF2 (Nuclear Factor-Erythroid 2 Like 2) is a transcription factor that orchestrates the cellular response to oxidative stress. The regulation of NRF2 signalling has been shown to be a promising strategy to modulate the progression of the neurodegeneration associated to Parkinson's disease. The NRF2 pathway has been shown to be affected in patients with this disease, and activation of NRF2 has neuroprotective effects in preclinical models, demonstrating the therapeutic potential of this pathway. In this review, we highlight recent advances regarding the regulation of NRF2, including the effect of Angiotensin II as an endogenous signalling molecule able to regulate ROS production and oxidative stress in dopaminergic neurons. The genes regulated and the downstream effects of activation, with special focus on Kruppel Like Factor 9 (KLF9) transcription factor, provide clues about the mechanisms involved in the neurodegenerative process as well as future therapeutic approaches.
Keyphrases
- oxidative stress
- transcription factor
- dna damage
- reactive oxygen species
- angiotensin ii
- diabetic rats
- nuclear factor
- ischemia reperfusion injury
- induced apoptosis
- cell death
- toll like receptor
- angiotensin converting enzyme
- multiple sclerosis
- genome wide
- bone marrow
- inflammatory response
- mesenchymal stem cells
- dna methylation
- dna binding
- signaling pathway
- white matter
- gene expression
- spinal cord
- immune response
- body mass index
- genome wide identification