Prototypic P2X7 Receptor Agonist, BzATP, Induced the Expression of Unfolded Protein Response Genes in Human M1 Macrophages

Maryam  Akhtari; Seyed Jalal Zargar; Ali Javinani; Amir  Ashraf-Ganjouei; Mahdi Vojdanian; Ahmadreza Jamshidi; Mahdi Mahmoudi

doi:10.18502/ijaai.v21i1.8618

Maryam Akhtari Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran
Seyed Jalal Zargar Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran
Ali Javinani Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
Amir Ashraf-Ganjouei Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
Mahdi Vojdanian Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
Ahmadreza Jamshidi Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
Mahdi Mahmoudi Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran

DOI: https://doi.org/10.18502/ijaai.v21i1.8618

Keywords: 3'-O-(4-benzoyl) benzoyladenosine 5'-triphosphate; Cell death; Purinergic receptors; Unfolded protein response

Abstract

Purinergic receptors stimulation by adenosine triphosphate (ATP) contributes significantly to macrophage activation, and also macrophage cell death. Upon the macrophage activation, the protein load of the endoplasmic reticulum is increased which is resulted in the activation of unfolded protein response (UPR). In the current study, we aimed to evaluate the connection between prototypic P2X₇ receptor agonist, extracellular 2ʹ(3ʹ)-O-(4-Benzoylbenzoyl)-ATP (BzATP), and the UPR pathway in macrophages.

The monocyte-derived macrophages from blood samples of 14 healthy volunteers were skewed toward M1 macrophages after incubation with LPS and IFN-γ. M1 macrophages were treated with 200 µM BzATP. The expression levels of UPR genes, including CHOP, HERP, GADD34, XBP1, and ATF6 in macrophages before and after treatment were measured using real-time polymerase chain reaction.

The results demonstrated that the expression of CHOP, HERP, and ATF6 is significantly decreased and the expression level of GADD34 and XBP1 is significantly increased after
M1 polarization. BzATP not only significantly increased the expression levels of CHOP, GADD34, ATF6, and HERP but also significantly decreases the XBP1 expression level in M1 macrophages.

The present study showed that BzATP induces cellular stress in M1 macrophages by
elevating the expression levels of UPR genes including CHOP, GADD34, ATF6, and reducing cell viability.