AI Article Synopsis

  • The P2X7 receptor is important in immune cells, linked to the release of cathepsin into macrophages, hinting at its role in lysosomal membrane permeabilization (LMP) and leakage.
  • This study revealed that high ATP concentrations (500 μM and 5 mM) trigger LMP in macrophages, but not in P2X7-deficient cells, indicating the receptor's essential role.
  • The research identified that P2X7 receptor and pannexin-1 channels cause calcium influx, which activates ion channels in late endosomes and lysosomes, leading to LMP and cathepsin release, emphasizing its significance in inflammation and infectious diseases.

Article Abstract

The P2X7 receptor is a critical purinergic receptor in immune cells. Its activation was associated with cathepsin release into macrophage cytosol, suggesting its involvement in lysosomal membrane permeabilization (LMP) and leakage. Nevertheless, the mechanisms by which P2X7 receptor activation induces LMP and leakage are unclear. This study investigated cellular mechanisms associated with endosomal and lysosomal leakage triggered by P2X7 receptor activation. We found that ATP at 500 μM and 5 mM (but not 50 μM) induced LMP in non-stimulated peritoneal macrophages. This effect was not observed in P2X7-deficient or A740003-pretreated macrophages. We found that the P2X7 receptor and pannexin-1 channels mediate calcium influx that might be important for activating specific ion channels (TRPM2 and two-pore channels) on the membranes of late endosomes and lysosomes leading to LMP leakage and consequent cathepsin release. These findings suggest the critical role of the P2X7 receptor in inflammatory and infectious diseases lysosomal dysfunction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863609PMC
http://dx.doi.org/10.3389/fimmu.2022.752105DOI Listing

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