The potassium channels Kv1.5 and Kv1.3 modulate distinct functions of microglia

Mol Cell Neurosci. 2006 Dec;33(4):401-11. doi: 10.1016/j.mcn.2006.08.009. Epub 2006 Oct 19.

Abstract

Activation of microglia by LPS leads to an induction of cytokine and NO release, reduced proliferation and increased outward K(+) conductance, the latter involving the activation of Kv1.5 and Kv1.3 channels. We studied the role of these channels for microglial function using two strategies to interfere with channel expression, a Kv1.5 knockout (Kv1.5(-/-)) mouse and an antisense oligonucleotide (AO) approach. The LPS-induced NO release was reduced by AO Kv1.5 and completely absent in the Kv1.5(-/-) animal; the AO Kv1.3 had no effect. In contrast, proliferation was augmented with both, loss of Kv1.3 or Kv1.5 channel expression. After facial nerve lesion, proliferation rate was higher in Kv1.5(-/-) animals as compared to wild type. Patch clamp experiments confirmed the reduction of the LPS-induced outward current amplitude in Kv1.5(-/-) microglia as well as in Kv1.5- or Kv1.3 AO-treated cells. Our study indicates that induction of K(+) channel expression is a prerequisite for the full functional spectrum of microglial activation.

MeSH terms

  • Animals
  • Brain / cytology
  • Bromodeoxyuridine / metabolism
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Dose-Response Relationship, Radiation
  • Electric Stimulation / methods
  • Embryo, Mammalian
  • Facial Nerve Diseases / metabolism
  • Facial Nerve Diseases / pathology
  • Immunohistochemistry / methods
  • Kv1.3 Potassium Channel / chemistry
  • Kv1.3 Potassium Channel / physiology*
  • Kv1.5 Potassium Channel / chemistry
  • Kv1.5 Potassium Channel / genetics
  • Kv1.5 Potassium Channel / physiology*
  • Lipopolysaccharides / pharmacology
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Membrane Potentials / radiation effects
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / drug effects
  • Microglia / physiology*
  • Nitric Oxide / metabolism
  • Oligodeoxyribonucleotides, Antisense / pharmacology
  • Patch-Clamp Techniques / methods
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods

Substances

  • Chemokines
  • Cytokines
  • Kv1.3 Potassium Channel
  • Kv1.5 Potassium Channel
  • Lipopolysaccharides
  • Oligodeoxyribonucleotides, Antisense
  • RNA, Messenger
  • Nitric Oxide
  • Bromodeoxyuridine