Ethanol differentially modulates P2X4 and P2X7 receptor activity and function in BV2 microglial cells

NEUROPHARMACOLOGY

卷:128

Article

Asatryan, Liana¹  Ostrovskaya, Olga²  Lieu, Dustin¹  Davies, Daryl L.¹ 

[1] Univ Southern Calif, Sch Pharm, Titus Family Dept Clin Pharm, Los Angeles, CA 90033 USA

[2] Univ Texas Austin, Ctr Learning & Memory, Austin, TX 78712 USA

关键词: Purinergic P2X4 and P2X7 receptors;    Ethanol;    BV2 microglia;    P2X antagonists;    IL-beta secretion;    Patch-clamp electrophysiology;   

DOI  :  10.1016/j.neuropharm.2017.09.030

来源: Elsevier

【 摘 要 】

Neuroinflammation is one of the mechanisms leading to neurodegenerative brain damage induced by chronic alcohol (ethanol) exposure. Microglia play a major role in the development of innate immune responses to environmental injuries including ethanol. Adenosine 5 ''-triphosphate (ATP)-activated purinergic P2X receptor (P2XR) subtypes, P2X4Rs and P2X7Rs, are endogenously expressed in microglia and can modulate their activity. These 2 P2XR subtypes differ pharmacologically and functionally: 1) P2X4Rs are activated at lower (<= 0.1 mM) whereas P2X7Rs - at higher (>= 1.0 mM) ATP concentrations; 2) P2X4R activation contributes to the release of brain derived neurotrophic factor and its role in tactile allodynia and neuropathic pain is demonstrated; 3) Due to its role in the secretion of pro-inflammatory IL-1 beta, P2X7Rs have been implicated in the development of neurodegenerative pathologies, pain and morphine tolerance. To date, the roles of individual P2XR subtypes in ethanol effects on microglia and the functional consequences are not completely understood. Based on the existing knowledge on the pharmacological and functional differences between P2X4Rs and P2X7Rs, the present work tested the hypothesis that P2X4Rs and P2X7Rs play differential roles in ethanol action in microglia. Effects of ethanol on P2X4R and P2X7R activity, expression and functional consequences were determined using murine BV2 microglial cells. Ethanol (>= 100 mM) inhibited P2X4Rs but was inactive on P2X7 channel activity. Ethanol (25, 100 mM) inhibited P2X4R-mediated microglia migration whereas it potentiated pore formation in P2X7Rs. Furthermore, ethanol (25, 100 mM) potentiated P2X7R-mediated IL-1 beta secretion from BV2 microglia. Ethanol also induced protein expression for both P2XR subtypes. Overall, the findings identify differential roles for P2X4Rs and P2X7Rs in regards to ethanol effects on microglia which may be linked to different stages of ethanol exposure. (C) 2017 Elsevier Ltd. All rights reserved.

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