Related Experiment Video
Updated: Jul 17, 2026

Determination of the Relative Cell Surface and Total Expression of Recombinant Ion Channels Using Flow Cytometry
Published on: September 28, 2016
Transient receptor potential cation channels in disease
Bernd Nilius1, Grzegorz Owsianik, Thomas Voets
1Department of Physiology, Campus Gasthuisberg, KULeuven, Leuven, Belgium. Bernd.Nilius@med.kuleuven.be
Abstract:
The transient receptor potential (TRP) superfamily consists of a large number of cation channels that are mostly permeable to both monovalent and divalent cations. The 28 mammalian TRP channels can be subdivided into six main subfamilies: the TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), and the TRPA (ankyrin) groups. TRP channels are expressed in almost every tissue and cell type and play an important role in the regulation of various cell functions. Currently, significant scientific effort is being devoted to understanding the physiology of TRP channels and their relationship to human diseases. At this point, only a few channelopathies in which defects in TRP genes are the direct cause of cellular dysfunction have been identified. In addition, mapping of TRP genes to susceptible chromosome regions (e.g., translocations, breakpoint intervals, increased frequency of polymorphisms) has been considered suggestive of the involvement of these channels in hereditary diseases. Moreover, strong indications of the involvement of TRP channels in several diseases come from correlations between levels of channel expression and disease symptoms. Finally, TRP channels are involved in some systemic diseases due to their role as targets for irritants, inflammation products, and xenobiotic toxins. The analysis of transgenic models allows further extrapolations of TRP channel deficiency to human physiology and disease. In this review, we provide an overview of the impact of TRP channels on the pathogenesis of several diseases and identify several TRPs for which a causal pathogenic role might be anticipated.
Insights
Transient receptor potential (TRP) channels are crucial for cell function and implicated in numerous diseases. Research is advancing our understanding of TRP channel roles in human health and disease pathogenesis.
Area of Science:
- Physiology
- Molecular Biology
- Genetics
Background:
- Transient receptor potential (TRP) channels are a large superfamily of cation channels vital for cellular functions.
- Mammalian TRP channels comprise 28 members across six subfamilies (TRPC, TRPV, TRPM, TRPP, TRPML, TRPA).
- These channels are widely expressed and play significant roles in regulating diverse cell functions.
Purpose of the Study:
- To review the impact of TRP channels on the pathogenesis of various human diseases.
- To identify specific TRP channels potentially involved in disease causation.
- To explore the link between TRP channel dysfunction and human pathologies.
Main Methods:
- Literature review of current research on TRP channel physiology and disease association.
- Analysis of genetic data, including gene mapping and polymorphisms, related to TRP channels and hereditary diseases.
- Examination of correlations between TRP channel expression levels and disease symptoms.
- Inclusion of data from transgenic models to extrapolate TRP channel deficiency effects.
Main Results:
- TRP channels are implicated in the pathogenesis of several systemic diseases.
- Defects in TRP genes can directly cause channelopathies and cellular dysfunction.
- Genetic associations and expression level correlations suggest TRP channel involvement in hereditary and other diseases.
- Transgenic models provide insights into TRP channel roles in human physiology and disease.
Conclusions:
- TRP channels are significantly involved in the pathogenesis of numerous human diseases.
- Further research is warranted to elucidate the causal roles of specific TRP channels in disease.
- Understanding TRP channel function is critical for developing therapeutic strategies for TRP-related disorders.
Related Concept Videos
Non-gated Ion Channels
Compared to the gated ion channels, the non-gated channels, also known as leakage or passive channels, have no gating mechanism.
Non-gated Ion Channels
Compared to the gated ion channels, the non-gated channels, also known as leakage or passive channels, have no gating mechanism.
Mechanically-gated Ion Channels
Mechanically-gated Ion Channels
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Ligand-gated Ion Channels
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that include the...
