Channelpedia

PubMed 19710528


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Kir2.1 , Kv1.3



Title: Characterisation of K+ currents in the C8-B4 microglial cell line and their regulation by microglia activating stimuli.

Authors: Simon Moussaud, Elisabeth Lamodière, Catherine Savage, Henning J Draheim

Journal, date & volume: Cell. Physiol. Biochem., 2009 , 24, 141-52

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19710528


Abstract
Microglia are the intrinsic immune cells of the brain. As such, they are crucially involved in neuro-protection as well as neuro-degeneration. Their activation leads to the induction of cytokine and chemokine release, the production of reactive oxygen species and nitric oxide and an increased outward potassium conductance. In this study, we focus our interest on potassium currents and channels in the C8-B4 murine microglial cell line and compare them with those of primary cultured microglia from neo-natal mice. Using the whole cell patch-clamp technique, we have recorded prominent inward and outward rectifying voltage-dependent potassium currents but no calcium-activated potassium currents. Using pharmacological, biophysical and molecular approaches, we demonstrate that Kv1.3 and Kir2.1 channels underlie outward and inward rectifying potassium currents, respectively. In contrast to primary cultured microglia, we observe that an outward rectifying potassium current is already present in unstimulated C8-B4 cells. However, as seen in primary microglia, this current increases after treatment with LPS, IFN-gamma, TGF-beta and GM-CSF and is suppressed by treatment with protein kinase inhibitors. Our study indicates that the C8-B4 cell line shows similar though not identical potassium channel properties compared to primary cultured microglia. We demonstrate that despite some differences, they are a useful tool to study potassium currents in microglial activation mechanisms by means of electrophysiological methods without the need for preparation of cells as primary culture.