Prion proteins: Physiological functions and role in neurological disorders

Abstract 

Stanley Prusiner was the first to promote the concept of misfolded proteins as a cause for neurological disease. It has since been shown by him and other investigators that the scrapie isoform of prion protein (PrP^Sc) functions as an infectious agent in numerous human and non-human disorders of the central nervous system (CNS). Interestingly, other organ systems appear to be less affected, and do not appear to lead to major co-morbidities. The physiological function of the endogenous cellular form of the prion protein (PrP^C) is much less clear. It is intriguing that PrP^c is expressed on most tissues in mammals, suggesting not only biological functions outside the CNS, but also a role other than the propagation of its misfolded isotype. In this review, we summarize accumulating in vitro and in vivo evidence regarding the physiological functions of PrP^C in the nervous system, as well as in lymphoid organs.

Keywords: Adaptive immunity, Aging, Alzheimer disease, Cognition, Down syndrome, Innate immunity, Lymphocytes, Neuroprotection, Primary progressive aphasia, Prion protein, Prnp, PrP, Wilson disease