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Open AccessJournal ArticleDOI

Pannexin 1 as a driver of inflammation and ischemia–reperfusion injury

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TLDR
Pannexin 1 (Panx1) is a ubiquitously expressed protein forming large conductance channels that are central to many distinct inflammation and injury responses as mentioned in this paper, and the ability of Panx1 to serve as a central component of many diverse physiologic responses has proven to be critically dependent on the context of expression, post-translational modification, interacting partners, and the mode of stimulation.
Abstract
Pannexin 1 (Panx1) is a ubiquitously expressed protein forming large conductance channels that are central to many distinct inflammation and injury responses. There is accumulating evidence showing ATP released from Panx1 channels, as well as metabolites, provide effective paracrine and autocrine signaling molecules that regulate different elements of the injury response. As channels with a broad range of permselectivity, Panx1 channels mediate the secretion and uptake of multiple solutes, ranging from calcium to bacterial derived molecules. In this review, we describe how Panx1 functions in response to different pro-inflammatory stimuli, focusing mainly on signaling coordinated by the vasculature. How Panx1 mediates ATP release by injured cells is also discussed. The ability of Panx1 to serve as a central component of many diverse physiologic responses has proven to be critically dependent on the context of expression, post-translational modification, interacting partners, and the mode of stimulation.

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Journal ArticleDOI

Effects of probenecid and brilliant blue G on rat enteric glial cells following intestinal ischemia and reperfusion.

TL;DR: In this paper , the effects of probenecid (PB) and brilliant blue G (BBG) on rat ileum enteric glial cells after on ischemia and reperfusion were examined.
Journal ArticleDOI

Probenecid-Blocked Pannexin-1 Channel Protects Against Early Brain Injury via Inhibiting Neuronal AIM2 Inflammasome Activation After Subarachnoid Hemorrhage

TL;DR: Pannexin-1 channel inhibitor probenecid attenuated brain edema and improved neurological dysfunction by reducing AIM2 inflammasome activation and reactive oxygen species (ROS) generation after SAH in rats.
Journal ArticleDOI

Pharmacology of pannexin channels.

TL;DR: A review of the state of the art for agents that can be used to block pannexin channels, with a focus on chemical pharmaceuticals and peptide mimetics that act on PAN 1 is presented in this paper .
Journal ArticleDOI

Pannexin1 channels—a potential therapeutic target in inflammation

TL;DR: Pannexin (Panx) channels have been shown to contribute to different modes of cell death (i.e., pyroptosis, necrosis and apoptosis) as discussed by the authors .
Journal ArticleDOI

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

Mathieu Vinken
- 01 Aug 2022 - 
TL;DR: In this article , the role of pannexin1 channels in chemical toxicity has been investigated, including metals, chelating agents, particulate matter, nanoparticles and drugs.
References
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Journal ArticleDOI

Myocardial Reperfusion Injury

TL;DR: This review focuses on the mechanisms of the injury, on attempts to protect the heart against it, and on promising new approaches to cardioprotection during percutaneous coronary intervention.
Journal ArticleDOI

Excitatory amino acids as a final common pathway for neurologic disorders.

TL;DR: In many neurologic disorders, injury to neurons may be caused at least in part by overstimulation of receptors for excitatory amino acids, including glutamate and aspartate.
Journal ArticleDOI

Ischemia and reperfusion—from mechanism to translation

TL;DR: Ischemia and reperfusion-elicited tissue injury contributes to morbidity and mortality in a wide range of pathologies, including myocardial infarction, ischemic stroke, acute kidney injury, trauma, circulatory arrest, sickle cell disease and sleep apnea as discussed by the authors.
Book ChapterDOI

Cell Biology of Ischemia/Reperfusion Injury

TL;DR: It is apparent that a combination of molecular and cellular approaches targeting multiple pathologic processes to limit the extent of I/R injury must be adopted to enhance resistance to cell death and increase regenerative capacity in order to effect long-lasting repair of ischemic tissues.
Journal ArticleDOI

Pannexin-1 mediates large pore formation and interleukin-1β release by the ATP-gated P2X7 receptor

TL;DR: Pannexin‐1, a recently described mammalian protein that functions as a hemichannel when ectopically expressed, is identified as this dye‐uptake pathway and signalling through pannexin•1 is required for processing of caspase‐1 and release of mature IL‐1β induced by P2X7 receptor activation.
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