Abstract
Selenoprotein P (SeP; encoded by SELENOP) is selenium (Se)-rich plasma protein that is mainly produced in the liver. SeP functions as a Se-transport protein to deliver Se from the liver to other tissues, such as the brain and testis. The protein plays a pivotal role in Se metabolism and antioxidative defense, and it has been identified as a 'hepatokine' that causes insulin resistance in type 2 diabetes. SeP levels are increased in type 2 diabetes patients, and excess SeP impairs insulin signalling, promoting insulin resistance. Furthermore, increased levels of SeP disturb the functioning of pancreatic β cells and inhibit insulin secretion. This review focuses on the biological function of SeP and the molecular mechanisms associated with the adverse effects of excess SeP on pancreatic β cells' function, particularly with respect to redox reactions. Interactions between the liver and pancreas are also discussed.
Original language | English |
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Pages (from-to) | 119-124 |
Number of pages | 6 |
Journal | Journal of Infectious Diseases |
Volume | 220 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2019 Aug 15 |
Keywords
- Selenoprotein P
- cell
- hepatokine
- insulin secretion
- pancreaticβ
- selenium
ASJC Scopus subject areas
- Immunology and Allergy
- Infectious Diseases