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Journal of Virology, August 2000, p. 7683-7686, Vol. 74, No. 16
Program in
Neuroscience1 and Departments of
Pediatrics2 and
Microbiology,3 University of Iowa,
Iowa City, Iowa 52242
Received 28 January 2000/Accepted 9 May 2000
Demyelination induced by mouse hepatitis virus (MHV), strain JHM,
is in large part immune mediated, but little is known about the
mechanisms involved in this process. Previous results suggest that
inducible nitric oxide synthase (NOS2) contributes transiently to
MHV-induced demyelination. Herein, we show that equivalent amounts of
demyelination were evident at day 12 after MHV infection in mice
genetically deficient in NOS2 (NOS2
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Coronavirus-Induced Demyelination Occurs in the
Absence of Inducible Nitric Oxide Synthase
/
) and in C57BL/6
mice. Furthermore, using an established adoptive transfer model and
pharmacological inhibitors of NOS2 function, we could demonstrate no
effect on MHV-induced demyelination. These results indicate that NOS2
function is not required for demyelination in mice infected with MHV.
*
Corresponding author. Mailing address: 2042 Medical
Labs, University of Iowa, Iowa City, IA 52242. Phone: (319) 335-8549. Fax: (319) 335-8991. E-mail: Stanley-Perlman{at}uiowa.edu.
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