AUTHOR=Espinosa Gabriel , Conejeros Iván , Rojas-Barón Lisbeth , Hermosilla Carlos Rodrigo , Taubert Anja 

TITLE=Besnoitia besnoiti-induced neutrophil clustering and neutrophil extracellular trap formation depend on P2X1 purinergic receptor signaling

JOURNAL=Frontiers in Immunology

VOLUME=14

YEAR=2023

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1244068

DOI=10.3389/fimmu.2023.1244068

ISSN=1664-3224

ABSTRACT=<p>Bovine besnoitiosis is a re-emerging cattle disease caused by the cyst-forming apicomplexan parasite <italic>Besnoitia besnoiti</italic>. Neutrophil extracellular trap (NET) formation represents an efficient innate immune mechanism of polymorphonuclear neutrophils (PMN) against apicomplexan parasites, including <italic>B. besnoiti</italic>. PMN purinergic signaling was proposed as a critical factor for NET formation. One important purinergic ligand is ATP, which is recognized as a danger signal and released into the extracellular space acting as an autocrine/paracrine signaling molecule. ATP-driven effects on PMN via the nucleotide P2 receptor family include chemotaxis, reactive oxygen species (ROS) production, and NET formation. So far, data on both PMN ATP concentrations and the role of ATP as a key modulator of purinergic signaling in <italic>B. besnoiti</italic> tachyzoite-triggered bovine NETosis is scarce. Current data showed that <italic>B. besnoiti</italic> tachyzoite exposure to bovine PMN neither changed total PMN ATP nor extracellular ATP quantities even though it significantly triggered NET formation. Moreover, <italic>B. besnoiti</italic> tachyzoite-exposed PMN revealed enhanced oxygen consumption rates (OCR) as quantified by the Seahorse metabolic analyzer. Exogenous supplementation of ATP or non-hydrolizable ATP (ATPγS) led to increased extracellular acidification rates (ECAR) but failed to alter tachyzoite-induced oxidative responses (OCR) in exposed PMN. In addition, exogenous supplementation of ATPγS, but not of ATP, boosted <italic>B. besnoiti</italic> tachyzoite-induced anchored NET formation. Referring to purinergic signaling, <italic>B. besnoiti</italic> tachyzoite-triggered anchored NET formation revealed P2X1 purinergic as receptor-dependent since it was blocked by the P2X1 inhibitor NF449 at an IC<sub>50</sub> of 1.27 µM. In contrast, antagonists of P2Y2, P2Y6, P2X4, and P2X7 purinergic receptors all failed to affect parasite-driven NETosis. As an interesting finding, we additionally observed that <italic>B. besnoiti</italic> tachyzoite exposure induced PMN clustering in a P2X1-dependent manner. Thus, we identified P2X1 purinergic receptor as a pivotal molecule for both <italic>B. besnoiti</italic> tachyzoite<italic>-</italic>induced PMN clustering and anchored NET formation.</p>