Journal of Neuroimmunology
Volume 229, Issue 1 , Pages 146-156, 15 December 2010

In vitro and in vivo induction and activation of nNOS by LPS in oligodendrocytes

  • S.Y. Yao

      Affiliations

    • Department of Neurology, Multiple Sclerosis Research Center, Nashville, TN 37212, USA
  • ,
  • A. Ljunggren-Rose

      Affiliations

    • Department of Neurology, Multiple Sclerosis Research Center, Nashville, TN 37212, USA
  • ,
  • N. Chandramohan

      Affiliations

    • Department of Neurology, Multiple Sclerosis Research Center, Nashville, TN 37212, USA
  • ,
  • W.O. Whetsell Jr.

      Affiliations

    • Department of Pathology, Vanderbilt University Medical Center, Nashville, TN 37212, USA
  • ,
  • S. Sriram

      Affiliations

    • Department of Neurology, Multiple Sclerosis Research Center, Nashville, TN 37212, USA
    • Corresponding Author InformationCorresponding author. Dept of Neurology, Vanderbilt Medical Center, Nashville, TN 37212, USA. Tel.: +1 615 963 4044; fax: +1 615 321 5247.

Received 19 May 2010; received in revised form 25 July 2010; accepted 27 July 2010. published online 20 August 2010.

Abstract 

There are currently four known isoforms of nitric oxide synthase (NOS). Of these, neuronal NOS (nNOS) is known to be present exclusively in neurons, endothelial NOS (eNOS) in vascular endothelium, while the inducible form of NOS (iNOS) is known to be activated in oligodendrocytes, astrocytes and microglia. The fourth isoform, mitochondrial NOS (mtNOS), represents a post-translational modification of nNOS. Using western blotting and real time-PCR, we show induction and activation of nNOS following culture of oligodendrocyte progenitor cells (OPC) with lipopolysaccharide (LPS). Activation of nNOS results in accumulation of peroxynitrite and tyrosine nitration of proteins in oligodendrocytes resulting in reduced cell viability. Injection of LPS in vivo into the corpus callosum of rats leads to the development of extensive demyelination of the white matter tracts. Immunostaining of regions close to the injection site shows the presence of nNOS, but not iNOS, in oligodendrocytes. Neither iNOS nor nNOS was seen in astrocytes in areas of demyelination. These studies suggest that activation of nNOS in oligodendrocytes leads to oligodendrocyte injury resulting in demyelination.

Keywords: Oligodendrocyte, LPS, nNOS, iNOS, Demyelination

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PII: S0165-5728(10)00336-X

doi:10.1016/j.jneuroim.2010.07.023

Journal of Neuroimmunology
Volume 229, Issue 1 , Pages 146-156, 15 December 2010