Activation of microglia cells is dispensable for the induction of rat retroviral spongiform encephalopathy

Journal of NeuroVirology - Tập 7 - Trang 501-510 - 2001
Regine Hansen1, Christian Sauder2, Stefanie Czub3, Eva Bachmann3, Simone Schimmer1, Annette Hegyi1, Markus Czub1,4
1Institut für Virologie und Immunbiologie, Universität Würzburg, Germany
2Abteilung Virologie, Institut für Medizinische Mikrobiologie und Hygiene der Albert-Ludwigs-Universität Freiburg, Germany
3Pathologisches Institut, Universität Würzburg, Germany
4Pathogenesis of biosafety level 4 agents, Canadian Science Centre for Human and Animal Health, Winnipeg, Canada

Tóm tắt

In the course of retroviral CNS infections, microglia activation has been observed frequently, and it has been hypothesized that activated microglia produce and secrete neurotoxic products like proinflammatory cytokines, by this promoting brain damage. We challenged this hypothesis in a rat model for neurodegeneration. In a kinetic study, we found that microglia cells of rats neonatally inoculated with neurovirulent murine leukemia virus (MuLV) NT40 became infected in vivo to maximal levels within 9–13 days postinoculation (bdd.p.i.). Beginning from 13 d.p.i., degenerative alterations, i.e., vacuolization of neurons and neuropil were found in cerebellar and other brain-stem nuclei. Elevated numbers of activated microglia cells—as revealed by immunohistochemical staining with monoclonal antibody EDI—were first detected at 19 d.p.i. and were always locally associated with degenerated areas but not with nonaltered, yet infected, brain regions. Both neuropathological changes and activated microglia cells increased in intensity and numbers, respectively, with ongoing infection but did not spread to other than initially affected brain regions. By ribonuclease protection assays, we were unable to detect differences in the expression levels of tumor-necrosis-factor-α (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) in microglia cells nor in total brains from infected versus uninfected rats. Our results suggest that the activation of microglia in the course of MuLV neurodegeneration is rather a reaction to, and not the cause of, neuronal damage. Furthermore, overt expression of the proinflammatory cytokines TNF-α, IL-1β, and IL-6 within the CNS is not required for the induction of retroviral associated neurodegeneration in rats.

Tài liệu tham khảo

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