TRP channels in disease
1KU Leuven, Department of Molecular Cell Biology, Division of Physiology, Laboratory of Ion Channel Research, Campus Gasthuisberg, Herestraat 49, bus 802, B-3000 Leuven, Belgium. Bernd.Nilius@med.kuleuven.be
Abstract:
"Transient receptor potential" cation channels (TRP channels) play a unique role as cell sensors, are involved in a plethora of Ca(2+)-mediated cell functions, and play a role as "gate-keepers" in many homeostatic processes such as Ca(2+) and Mg(2+) reabsorption. The variety of functions to which TRP channels contribute and the polymodal character of their activation predict that failures in correct channel gating or permeation will likely contribute to complex pathophysiological mechanisms. Dysfunctions of TRPs cause human diseases but are also involved in a complex manner to contribute and determine the progress of several diseases. Contributions to this special issue discuss channelopathias for which mutations in TRP channels that induce "loss-" or "gain-of-function" of the channel and can be considered "disease-causing" have been identified. The role of TRPs will be further elucidated in complex diseases of the intestinal, renal, urogenital, respiratory, and cardiovascular systems. Finally, the role of TRPs will be discussed in neuronal diseases and neurodegenerative disorders.
Insights
Transient receptor potential (TRP) channels are vital cell sensors involved in numerous functions. TRP channel dysfunction contributes to various human diseases, including channelopathies and complex systemic disorders.
Area of Science:
- Physiology
- Molecular Biology
- Biochemistry
Background:
- Transient receptor potential (TRP) channels function as polymodal cellular sensors.
- They are crucial for calcium (Ca2+) and magnesium (Mg2+) homeostasis and Ca2+-mediated cell functions.
- TRP channel dysfunctions are implicated in various human diseases.
Purpose of the Study:
- To explore the role of TRP channels in human diseases, focusing on channelopathies.
- To investigate the contribution of TRP channel dysfunction to complex diseases across multiple organ systems.
- To discuss the involvement of TRP channels in neurological and neurodegenerative disorders.
Main Methods:
- Review of existing literature on TRP channel mutations and associated diseases.
- Analysis of studies detailing TRP channel involvement in intestinal, renal, urogenital, respiratory, and cardiovascular systems.
- Examination of research on TRP channels in neuronal and neurodegenerative conditions.
Main Results:
- Identified specific TRP channel mutations causing 'loss-of-function' or 'gain-of-function' leading to channelopathies.
- Highlighted the complex role of TRP channels in the pathogenesis of systemic diseases.
- Underscored the significance of TRP channels in the progression of neurological disorders.
Conclusions:
- TRP channel dysfunction is a significant factor in human disease development and progression.
- Further research into TRP channels is crucial for understanding and treating a wide range of pathologies.
- TRP channels represent promising therapeutic targets for channelopathies and complex diseases.
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