APOPTOSIS IN ACUTE AND CHRONIC CENTRAL-NERVOUS-SYSTEM DISEASE INDUCEDBY THEILERS MURINE ENCEPHALOMYELITIS VIRUS

Citation
I. Tsunoda et al., APOPTOSIS IN ACUTE AND CHRONIC CENTRAL-NERVOUS-SYSTEM DISEASE INDUCEDBY THEILERS MURINE ENCEPHALOMYELITIS VIRUS, Virology, 228(2), 1997, pp. 388-393
Citations number
34
Categorie Soggetti
Virology
Journal title
ISSN journal
00426822
Volume
228
Issue
2
Year of publication
1997
Pages
388 - 393
Database
ISI
SICI code
0042-6822(1997)228:2<388:AIAACC>2.0.ZU;2-N
Abstract
Apoptosis has been observed in neural development and in various neuro logical diseases, including viral infection and multiple sclerosis. Th eiler's murine encephalomyelitis virus is divided into two subgroups b ased on neurovirulence: the highly neurovirulent GDVII strain produces an acute fatal polioencephalomyelitis in mice, whereas the attenuated DA strain produces demyelination with virus persistence preceded by a n acute infection. TUNEL combined with immunocytochemistry was used to detect apoptosis in the central nervous system and to characterize wh ich cell types were involved during the acute stage in both GDVII and DA virus infection and during the chronic stage in DA virus infection. We found that during the acute stage, apoptosis was induced in neuron s in both virus infections. However, the number of apoptotic neurons w as much greater in GDVII virus-infected mice than in DA virus-infected mice (P < 0.01). During the chronic stage of DA virus infection, apop totic cells were detected only in the spinal cord white matter. Some o f these cells were dual labeled for fragmented DNA and carbonic anhydr ase II, an oligodendrocyte marker. Our results indicate that apoptosis of neurons could be responsible for the fatal outcome in GDVII virus infection. In contrast, apoptosis of oligodendrocytes can contribute t o the chronic demyelinating DA virus infection. (C) 1997 Academic Pres s.