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Paracrine Stimulation of P2X7 Receptor by ATP Activates a Proliferative Pathway in Ovarian Carcinoma Cells
Author(s) -
VázquezCuevas Francisco G.,
MartínezRamírez Angélica S.,
RoblesMartínez Leticia,
Garay Edith,
GarcíaCarrancá Alejandro,
PérezMontiel Delia,
CastañedaGarcía Carolina,
Arellano Rogelio O.
Publication year - 2014
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.24867
Subject(s) - apyrase , purinergic receptor , autocrine signalling , apoptosis , viability assay , paracrine signalling , biology , stimulation , cell culture , microbiology and biotechnology , medicine , receptor , endocrinology , cancer research , extracellular , biochemistry , genetics
ABSTRACT P2X7 is a purinergic receptor‐channel; its activation by ATP elicits a broad set of cellular actions, from apoptosis to signals for survival. Here, P2X7 expression and function was studied in human ovarian carcinoma (OCA) cells, and biopsies from non‐cancerous and cancer patients were analyzed by immunohistochemistry. Ovarian surface epithelium in healthy tissue expressed P2X7 at a high level that was maintained throughout the cancer. The cell lines SKOV‐3 and CAOV‐3 were used to investigate P2X7 functions in OCA. In SKOV‐3 cells, selective stimulation of P2X7 by 2′(3′)‐O‐(4‐benzoylbenzoyl) adenosine‐5′‐triphosphate (BzATP) induced a dose‐dependent increase of intracellular Ca 2+ concentration ([Ca 2+ ] i ) but not cell death. Instead, BzATP increased the levels of phosphorylated ERK and AKT (pERK and pAKT), with an EC 50 of 44 ± 2 and 1.27 ± 0.5 μM, respectively; 10 μM BzATP evoked a maximum effect within 15 min that lasted for 120 min. Interestingly, basal levels of pERK and pAKT were decreased in the presence of apyrase in the medium, strongly suggesting an endogenous, ATP‐mediated phenomenon. Accordingly: (i) mechanically stimulated cells generated a [Ca 2+ ] i increase that was abolished by apyrase; (ii) apyrase induced a decrease in culture viability, as measured by the MTS assay for mitochondrial activity; and (iii) incubation with 10 μM AZ10606120, a specific P2X7 antagonist and transfection with the dominant negative P2X7 mutant E496A, both reduced cell viability to 70.1 ± 8.9% and to 76.5 ± 5%, respectively, of control cultures. These observations suggested that P2X7 activity was auto‐induced through ATP efflux; this increased pERK and pAKT levels that generated a positive feedback on cell viability. J. Cell. Biochem. 115: 1955–1966, 2014. © 2014 Wiley Periodicals, Inc.