ATP Is Required and Advances Cytokine-Induced Gap Junction Formation in Microglia In Vitro
Journal
Mediators of Inflammation
ISSN
0962-9351
1466-1861
Date Issued
2013
Author(s)
Pablo J. Sáez
Kenji F. Shoji
Paloma A. Harcha
Gigliola Ramírez
Jean X. Jiang
Rommy von Bernhardi
Juan C. Sáez
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Abstract
<jats:p>Microglia are the immune cells in the central nervous system. After injury microglia release bioactive molecules, including cytokines and ATP, which modify the functional state of hemichannels (HCs) and gap junction channels (GJCs), affecting the intercellular communication via extracellular and intracellular compartments, respectively. Here, we studied the role of extracellular ATP and several cytokines as modulators of the functional state of microglial HCs and GJCs using dye uptake and dye coupling techniques, respectively. In microglia and the microglia cell line EOC20, ATP advanced the TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>/IFN-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M2"><mml:mrow><mml:mi>γ</mml:mi></mml:mrow></mml:math>-induced dye coupling, probably through the induction of IL-1<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M3"><mml:mrow><mml:mi>β</mml:mi></mml:mrow></mml:math>release. Moreover, TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M4"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>/IFN-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M5"><mml:mrow><mml:mi>γ</mml:mi></mml:mrow></mml:math>, but not TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M6"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>plus ATP, increased dye uptake in EOC20 cells. Blockade of Cx43 and Panx1 HCs prevented dye coupling induced by TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M7"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>/IFN-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M8"><mml:mrow><mml:mi>γ</mml:mi></mml:mrow></mml:math>, but not TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M9"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>plus ATP. In addition, IL-6 prevented the induction of dye coupling and HC activity induced by TNF-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M10"><mml:mrow><mml:mi>α</mml:mi></mml:mrow></mml:math>/IFN-<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M11"><mml:mrow><mml:mi>γ</mml:mi></mml:mrow></mml:math>in EOC20 cells. Our data support the notion that extracellular ATP affects the cellular communication between microglia through autocrine and paracrine mechanisms, which might affect the timing of immune response under neuroinflammatory conditions.</jats:p>
Subjects
necrosis-factor-alpha
;
interferon-gamma
;
ifn-gamma
;
extracellular atp
;
p2x(7) receptor
;
intercellular communication
;
interleukin-1-beta release
;
connexin-43 hemichannels
;
activated microglia
;
dendritic cells