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TRPM5 in the battle against diabetes and obesity
R Vennekens1,2, M Mesuere1,2, K Philippaert1,2
1VIB Center for Brain & Disease Research, Leuven, Belgium.
Abstract:
TRPM5 is a non-selective monovalent cation channel activated by increases in intracellular Ca2+ . It has a distinct expression pattern: expression is detected in chemosensitive tissues from solitary chemosensory cells to the taste receptor cells and in pancreatic β-cells. The role of TRPM5 has been investigated with the use of knockout mouse models. Trpm5-/- mice have a lack of type II taste perception and show reduced glucose-induced insulin secretion. Expression levels of TRPM5 are reduced in obese, leptin-signalling-deficient mice, and mutations in TRPM5 have been associated with type II diabetes and metabolic syndrome. In this review, we aim to give an overview of the activation, selectivity, modulation and physiological roles of TRPM5.
Insights
Transient Receptor Potential Melastatin 5 (TRPM5) channels regulate taste perception and insulin secretion. Knockout mice lacking TRPM5 exhibit impaired taste and reduced glucose-induced insulin release, highlighting its physiological importance.
Area of Science:
- Physiology
- Molecular Biology
- Cell Biology
Background:
- TRPM5 is a non-selective monovalent cation channel.
- It is activated by intracellular calcium (Ca2+).
- TRPM5 is expressed in taste receptor cells and pancreatic beta-cells.
Purpose of the Study:
- To review the activation, selectivity, modulation, and physiological roles of TRPM5.
- To summarize findings from TRPM5 knockout mouse models.
Main Methods:
- Investigation using Trpm5 knockout mouse models.
- Analysis of taste perception in knockout mice.
- Assessment of glucose-induced insulin secretion in knockout mice.
Main Results:
- Trpm5-/- mice lack type II taste perception.
- Reduced glucose-induced insulin secretion was observed in Trpm5-/- mice.
- Reduced TRPM5 expression is linked to obesity and metabolic syndrome.
Conclusions:
- TRPM5 plays a critical role in taste perception and insulin secretion.
- Dysfunction of TRPM5 is associated with type II diabetes and metabolic syndrome.
- Further research into TRPM5 modulation could offer therapeutic strategies.
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