P2X7 receptor and the NLRP3 inflammasome: Partners in crime.

Abstract:

:Adenosine triphosphate (ATP) is a molecule that on one hand plays a central role in cellular energetics and which on the other is a ubiquitous signaling molecule when released into the extracellular media. Extracellular ATP accumulates in inflammatory environments where it acts as a damage-associated molecular pattern and activates the purinergic P2X receptor 7 (P2X7) in immune cells. P2X7 receptor activation induces the formation of the nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing 3 (NLRP3) inflammasome and the activation of the inflammatory caspase-1. Caspase-1 causes an inflammatory type of cell death called pyroptosis through the release of pro-inflammatory cytokines and intracellular content. Consequently, intense research efforts have been devoted to the design of novel anti-inflammatory therapies, focusing in particular on the P2X7 receptor and the NLRP3 pathway and the introduction of new blocking molecules in early phase clinical trials.

journal_name

Biochem Pharmacol

journal_title

Biochemical pharmacology

authors

Pelegrin P

doi

10.1016/j.bcp.2020.114385

subject

Has Abstract

pub_date

2020-12-20 00:00:00

pages

114385

eissn

0006-2952

issn

1873-2968

pii

S0006-2952(20)30621-3

pub_type

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