Format

Send to

Choose Destination
FEBS Lett. 2014 Apr 17;588(8):1416-22. doi: 10.1016/j.febslet.2014.03.009. Epub 2014 Mar 15.

The role of pannexin1 in the induction and resolution of inflammation.

Author information

1
Department of Pharmacology, University of Virginia, United States.
2
Department of Pharmacology, University of Virginia, United States. Electronic address: nl2q@virginia.edu.

Abstract

Extracellular ATP is an important signaling molecule throughout the inflammatory cascade, serving as a danger signal that causes activation of the inflammasome, enhancement of immune cell infiltration, and fine-tuning of several signaling cascades including those important for the resolution of inflammation. Recent studies demonstrated that ATP can be released from cells in a controlled manner through pannexin (Panx) channels. Panx1-mediated ATP release is involved in inflammasome activation and neutrophil/macrophage chemotaxis, activation of T cells, and a role for Panx1 in inducing and propagating inflammation has been demonstrated in various organs, including lung and the central and peripheral nervous system. The recognition and clearance of dying cells and debris from focal points of inflammation is critical in the resolution of inflammation, and Panx1-mediated ATP release from dying cells has been shown to recruit phagocytes. Moreover, extracellular ATP can be broken down by ectonucleotidases into ADP, AMP, and adenosine, which is critical in the resolution of inflammation. Together, Panx1, ATP, purinergic receptors, and ectonucleotidases contribute to important feedback loops during the inflammatory response, and thus represent promising candidates for new therapies.

KEYWORDS:

Extracellular ATP; Inflammation; Pannexin 1; Resolution

PMID:
24642372
PMCID:
PMC4060616
DOI:
10.1016/j.febslet.2014.03.009
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Wiley Icon for PubMed Central
Loading ...
Support Center