| Literature DB >> 33732108 |
Ulrich Schweizer1, Simon Bohleber1, Wenchao Zhao1, Noelia Fradejas-Villar1.
Abstract
Eighteen years ago, unexpected epileptic seizures in Selenop-knockout mice pointed to a potentially novel, possibly underestimated, and previously difficult to study role of selenium (Se) in the mammalian brain. This mouse model was the key to open the field of molecular mechanisms, i.e., to delineate the roles of selenium and individual selenoproteins in the brain, and answer specific questions like: how does Se enter the brain; which processes and which cell types are dependent on selenoproteins; and, what are the individual roles of selenoproteins in the brain? Many of these questions have been answered and much progress is being made to fill remaining gaps. Mouse and human genetics have together boosted the field tremendously, in addition to traditional biochemistry and cell biology. As always, new questions have become apparent or more pressing with solving older questions. We will briefly summarize what we know about selenoproteins in the human brain, glance over to the mouse as a useful model, and then discuss new questions and directions the field might take in the next 18 years.Entities:
Keywords: GPX4; epilepsy; ferroptosis; genetics; neurodegeneration
Year: 2021 PMID: 33732108 PMCID: PMC7959785 DOI: 10.3389/fnins.2021.652099
Source DB: PubMed Journal: Front Neurosci ISSN: 1662-453X Impact factor: 4.677