Oxidative stress management in the hair follicle: Could targeting NRF2 counter age-related hair disorders and beyond?
Laura JadkauskaitePierre A CoulombeMatthias SchäferAlbena T Dinkova-KostovaRalf PausIain S HaslamPublished in: BioEssays : news and reviews in molecular, cellular and developmental biology (2017)
Widespread expression of the transcription factor, nuclear factor (erythroid-derived 2)-like 2 (NRF2), which maintains redox homeostasis, has recently been identified in the hair follicle (HF). Small molecule activators of NRF2 may therefore be useful in the management of HF pathologies associated with redox imbalance, ranging from HF greying and HF ageing via androgenetic alopecia and alopecia areata to chemotherapy-induced hair loss. Indeed, NRF2 activation has been shown to prevent peroxide-induced hair growth inhibition. Multiple parameters can increase the levels of reactive oxygen species in the HF, for example melanogenesis, depilation-induced trauma, neurogenic and autoimmune inflammation, toxic drugs, environmental stressors such as UV irradiation, genetic defects and aging-associated mitochondrial dysfunction. In this review, the potential mechanisms whereby NRF2 activation could prove beneficial in treatment of redox-associated HF disorders are therefore discussed.
Keyphrases
- oxidative stress
- diabetic rats
- acute heart failure
- small molecule
- nuclear factor
- transcription factor
- reactive oxygen species
- ischemia reperfusion injury
- induced apoptosis
- dna damage
- toll like receptor
- chemotherapy induced
- drug induced
- high glucose
- poor prognosis
- spinal cord injury
- human health
- heart failure
- genome wide
- gene expression
- climate change
- binding protein
- endoplasmic reticulum stress
- inflammatory response
- endothelial cells
- radiation induced
- dna binding
- long non coding rna