Astrocytic JWA expression is essential to dopaminergic neuron survival in the pathogenesis of Parkinson's disease

CNS Neurosci Ther. 2014 Aug;20(8):754-62. doi: 10.1111/cns.12249. Epub 2014 Mar 17.

Abstract

Aims: To investigate the role of astrocytic JWA expression in dopaminergic (DA) neuron degeneration and in the pathogenesis of Parkinson's disease (PD).

Methods: Conditional astrocytic JWA null (JWA∆2/∆2/GFAP-Cre) mice and U251 glioma cells were used to evaluate the effects of JWA gene on DA neuron degeneration. The oxidative stress-driven molecular events were determined in both in vivo and in vitro models.

Results: Conditional astrocytic JWA knockout resulted in significant activation of astrocytes measured by increase in glial fibrillary acidic protein-positive cells (1.34×10(3)±74.5 vs. 8.44×10(3)±1.35×10(3), P<0.01) in mouse substantia nigra, accompanied by loss of DA neurons (1.03×10(4)±238 vs. 6.17×10(3)±392, P<0.001). Deficiency of JWA significantly aggravated reactive oxygen species (ROS) accumulation in substantia nigra compared with the wild-type mice. Increasing JWA expression in U251 glioma cells inhibited ROS with a concomitant increase in intracellular glutathione. Furthermore, suppression of IKKβ-nuclear factor (NF)-κB signaling pathway was shown to regulate JWA in a PD model.

Conclusions: The JWA gene exerts neuroprotective roles against DA neuronal degeneration via modulating intracellular redox status and NF-κB signaling pathway and is a potential treatment target for PD.

Keywords: Dopamine; JWA; NF-κB; Parkinson's disease; Reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3,4-Dihydroxyphenylacetic Acid / metabolism
  • Animals
  • Astrocytes / metabolism*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Line
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Disease Models, Animal
  • Dopamine / metabolism*
  • Glial Fibrillary Acidic Protein / genetics
  • Glial Fibrillary Acidic Protein / metabolism
  • Glutathione / metabolism
  • Heat-Shock Proteins
  • Homovanillic Acid / metabolism
  • I-kappa B Kinase / metabolism
  • MPTP Poisoning / pathology*
  • Membrane Transport Proteins
  • Mice
  • Mice, Transgenic
  • Neurons / pathology*
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Substantia Nigra / pathology
  • Transfection

Substances

  • Arl6ip5 protein, mouse
  • Carrier Proteins
  • Glial Fibrillary Acidic Protein
  • Heat-Shock Proteins
  • Membrane Transport Proteins
  • Reactive Oxygen Species
  • 3,4-Dihydroxyphenylacetic Acid
  • I-kappa B Kinase
  • Glutathione
  • Dopamine
  • Homovanillic Acid