HIV-1 Tat protein increases microglial outward K(+) current and resultant neurotoxic activity

PLoS One. 2013 May 30;8(5):e64904. doi: 10.1371/journal.pone.0064904. Print 2013.

Abstract

Microglia plays a crucial role in the pathogenesis of HIV-1-associated neurocognitive disorders. Increasing evidence indicates the voltage-gated potassium (Kv) channels are involved in the regulation of microglia function, prompting us to hypothesize Kv channels may also be involved in microglia-mediated neurotoxic activity in HIV-1-infected brain. To test this hypothesis, we investigated the involvement of Kv channels in the response of microglia to HIV-1 Tat protein. Treatment of rat microglia with HIV-1 Tat protein (200 ng/ml) resulted in pro-inflammatory microglial activation, as indicated by increases in TNF-α, IL-1β, reactive oxygen species, and nitric oxide, which were accompanied by enhanced outward K(+) current and Kv1.3 channel expression. Suppression of microglial Kv1.3 channel activity, either with Kv1.3 channel blockers Margatoxin, 5-(4-Phenoxybutoxy)psoralen, or broad-spectrum K(+) channel blocker 4-Aminopyridine, or by knockdown of Kv1.3 expression via transfection of microglia with Kv1.3 siRNA, was found to abrogate the neurotoxic activity of microglia resulting from HIV-1 Tat exposure. Furthermore, HIV-1 Tat-induced neuronal apoptosis was attenuated with the application of supernatant collected from K(+) channel blocker-treated microglia. Lastly, the intracellular signaling pathways associated with Kv1.3 were investigated and enhancement of microglial Kv1.3 was found to correspond with an increase in Erk1/2 mitogen-activated protein kinase activation. These data suggest targeting microglial Kv1.3 channels may be a potential new avenue of therapy for inflammation-mediated neurological disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Electrophysiological Phenomena / drug effects*
  • Gene Knockdown Techniques
  • HIV-1*
  • Kv1.3 Potassium Channel / antagonists & inhibitors
  • Kv1.3 Potassium Channel / deficiency
  • Kv1.3 Potassium Channel / genetics
  • Kv1.3 Potassium Channel / metabolism
  • MAP Kinase Signaling System / drug effects
  • Microglia / cytology
  • Microglia / drug effects*
  • Microglia / metabolism*
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurotoxins / toxicity*
  • Potassium / metabolism*
  • Potassium Channel Blockers / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation / drug effects
  • tat Gene Products, Human Immunodeficiency Virus / toxicity*

Substances

  • Kv1.3 Potassium Channel
  • Neurotoxins
  • Potassium Channel Blockers
  • tat Gene Products, Human Immunodeficiency Virus
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Potassium