Toxic talk: pannexin1 channel communication as an emerging mechanism of toxicity

Mathieu Vinken1

  • 1Department of Pharmaceutical and Pharmacological Sciences, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.

Toxicology
|August 23, 2022
PubMed

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.

Related Concept Videos

Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
2.5K
Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
11.2K
Chemical Synapses01:26

Chemical Synapses

Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
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...
3.1K
Ligand-gated Ion Channels01:19

Ligand-gated Ion Channels

Ligand-gated ion channels are transmembrane proteins with a channel for ions to pass through and a binding site for a ligand. The channel opens only when a ligand attaches to the binding site.
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...
12.6K
Resting Membrane Potential01:24

Resting Membrane Potential

The relative difference in electrical charge, or voltage, between the inside and the outside of a cell membrane, is called the membrane potential. It is generated by differences in permeability of the membrane to various ions and the concentrations of these ions across the membrane.
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...
19.1K
Voltage-gated Ion Channels01:26

Voltage-gated Ion Channels

Voltage-gated ion channels are transmembrane proteins that open and close in response to changes in the membrane potential. They are present on the membranes of all electrically excitable cells such as neurons, heart, and muscle cells.
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...
8.5K