New Light on Prions: Putative Role of PrP c in Pathophysiology of Mood Disorders.
Adrian Andrzej ChrobakPatrycja Pańczyszyn-TrzewikPatrycja KrólMagdalena Pawelec-BąkDominika DudekMarcin SiwekPublished in: International journal of molecular sciences (2024)
Mood disorders are highly prevalent and heterogenous mental illnesses with devastating rates of mortality and treatment resistance. The molecular basis of those conditions involves complex interplay between genetic and environmental factors. Currently, there are no objective procedures for diagnosis, prognosis and personalization of patients' treatment. There is an urgent need to search for novel molecular targets for biomarkers in mood disorders. Cellular prion protein (PrP c ) is infamous for its potential to convert its insoluble form, leading to neurodegeneration in Creutzfeldt-Jacob disease. Meanwhile, in its physiological state, PrP c presents neuroprotective features and regulates neurotransmission and synaptic plasticity. The aim of this study is to integrate the available knowledge about molecular mechanisms underlying the impact of PrP c on the pathophysiology of mood disorders. Our review indicates an important role of this protein in regulation of cognitive functions, emotions, sleep and biological rhythms, and its deficiency results in depressive-like behavior and cognitive impairment. PrP c plays a neuroprotective role against excitotoxicity, oxidative stress and inflammation, the main pathophysiological events in the course of mood disorders. Research indicates that PrP c may be a promising biomarker of cognitive decline. There is an urgent need of human studies to elucidate its potential utility in clinical practice.
Keyphrases
- bipolar disorder
- platelet rich plasma
- cognitive decline
- sleep quality
- oxidative stress
- cognitive impairment
- end stage renal disease
- clinical practice
- mild cognitive impairment
- endothelial cells
- ejection fraction
- newly diagnosed
- cardiovascular events
- chronic kidney disease
- dna damage
- mental health
- prognostic factors
- physical activity
- gene expression
- type diabetes
- ischemia reperfusion injury
- peritoneal dialysis
- cardiovascular disease
- risk factors
- brain injury
- dna methylation
- copy number
- patient reported