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Amyloid‐β‐induced reactive oxygen species production and priming are differentially regulated by ion channels in microglia
Author(s) -
Schilling Tom,
Eder Claudia
Publication year - 2011
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.22675
Subject(s) - microglia , reactive oxygen species , ion channel , priming (agriculture) , chemistry , amyloid β , amyloid (mycology) , oxygen , microbiology and biotechnology , ion , superoxide , biophysics , neuroscience , biochemistry , biology , inflammation , immunology , medicine , enzyme , disease , botany , receptor , germination , inorganic chemistry , organic chemistry
Abstract Production of reactive oxygen species (ROS) by microglial cells and subsequent oxidative stress are strongly implicated in the pathogenesis of Alzheimer's disease. Although it is recognized that amyloid‐β (Aβ) plays a major role in inducing and regulating microglial ROS production in Alzheimer's disease, to date little is known about cellular mechanisms underlying Aβ‐stimulated ROS production. Here, we identified ion channels involved in Aβ‐induced microglial ROS production and in Aβ‐induced microglial priming. Acute stimulation of microglial cells with either fibrillar Aβ 1–42 (fAβ 1–42 ) or soluble Aβ 1–42 (sAβ 1–42 ) caused significant increases in microglial ROS production, which were abolished by inhibition of TRPV1 cation channels with 5‐iodo‐resiniferatoxin (I‐RTX), but were unaffected by inhibition of K + channels with charybdotoxin (CTX). Furthermore, pretreatment with either fAβ 1–42 or sAβ 1–42 induced microglial priming, that is, increased ROS production upon secondary stimulation with the phorbol ester PMA. Microglial priming induced by fAβ 1–42 or sAβ 1–42 remained unaffected by TRPV1 channel inhibition with I‐RTX. However, sAβ 1–42 ‐induced priming was inhibited by CTX and margatoxin, but not by TRAM‐34 or paxilline, indicating a role of Kv1.3 voltage‐gated K + channels, but not of Ca 2+ ‐activated K + channels, in the priming process. In summary, our data suggest that in microglia Aβ‐induced ROS production and priming are differentially regulated by ion channels, and that TRPV1 cation channels and Kv1.3 K + channels may provide potential therapeutic targets to reduce microglia‐induced oxidative stress in Alzheimer's disease. J. Cell. Physiol. 226: 3295–3302, 2011. © 2011 Wiley Periodicals, Inc.