Related Experiment Video
Updated: Aug 31, 2025

Proteomics to Identify Proteins Interacting with P2X2 Ligand-Gated Cation Channels
Published on: May 18, 2009
Toxic talk: pannexin1 channel communication as an emerging mechanism of toxicity
1Department of Pharmaceutical and Pharmacological Sciences, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.
Abstract:
Pannexin1 channels facilitate the extracellular release of a number of messengers, including adenosine triphosphate. Although fulfilling some physiological functions, pannexin1 channel communication has to date been primarily studied in the context of inflammation and cell death. In the past decade, a variety of chemical substances have been reported to induce pannexin1 channel opening, including metals, chelating agents, particulate matter, nanoparticles and drugs. While the pathophysiological aspects of pannexin1 channel communication have been reviewed on many previous occasions, the present paper intends to provide a short perspective in order to motivate research that will advance mechanistic understanding of the roles of pannexin1 signaling in chemical toxicity.
Insights
Pannexin1 channels release signaling molecules like ATP. This review explores how chemicals trigger pannexin1 channel opening, highlighting their role in chemical toxicity and prompting further research into signaling mechanisms.
Area of Science:
- Cellular signaling
- Toxicology
- Molecular biology
Background:
- Pannexin1 channels mediate extracellular release of signaling molecules, notably adenosine triphosphate (ATP).
- While involved in physiological functions, pannexin1 channel activity is predominantly studied in relation to inflammation and cell death.
- Numerous chemical agents, including metals, nanoparticles, and drugs, are known to induce pannexin1 channel opening.
Purpose of the Study:
- To provide a concise perspective on pannexin1 channel signaling.
- To stimulate research into the mechanistic roles of pannexin1 signaling in chemical toxicity.
- To bridge the gap between known chemical triggers and the underlying mechanisms of pannexin1 channel activation in toxicological contexts.
Main Methods:
- Literature review and synthesis of existing research on pannexin1 channel activators.
- Analysis of reported chemical substances that induce pannexin1 channel opening.
- Identification of knowledge gaps in understanding the mechanistic basis of chemical-induced pannexin1 signaling.
Main Results:
- A diverse range of chemical substances can modulate pannexin1 channel activity.
- The specific mechanisms by which these chemicals activate pannexin1 channels remain largely unelucidated.
- Existing research has primarily focused on the pathological consequences rather than the molecular mechanisms of chemical-induced pannexin1 signaling.
Conclusions:
- Pannexin1 channels are implicated in cellular responses to various chemical exposures.
- Further mechanistic research is crucial to understand pannexin1 signaling in chemical toxicity.
- Elucidating these mechanisms will advance our understanding of cellular responses to environmental and therapeutic chemical agents.
More Related Videos
10:46Mechanical Stimulation-induced Calcium Wave Propagation in Cell Monolayers: The Example of Bovine Corneal Endothelial Cells
Published on: July 16, 2013
10:20Method for Identifying Small Molecule Inhibitors of the Protein-protein Interaction Between HCN1 and TRIP8b
Published on: November 11, 2016
Related Concept Videos
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Fusion of Secretory Vesicles with the Plasma Membrane
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
Chemical Synapses
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
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...
Resting Membrane Potential
The Inside of a Neuron is More Negative
The membrane potential of a cell can be measured by inserting a microelectrode into a cell and comparing the charge to a reference electrode in the extracellular fluid. The...
Voltage-gated Ion Channels
Generally, all voltage-gated ion channels have a 'voltage-sensing domain' that spans the lipid bilayer. The charged residues in the sensor move in response to the membrane potential changes that open the channel allowing ions movement. There are several...