Key result
Activated astrocytes present TMEV epitopes to T cells, inducing IFN-gamma production and subsequent Fas-dependent lysis of astrocytes, potentially compromising the blood-brain barrier.
Astrocytes may play a key role in TMEV-induced demyelination by activating T cells, which subsequently leads to T cell-mediated apoptosis of astrocytes and blood-brain barrier compromise.
May implicate astrocytes in viral demyelination; extends TMEV model data but leaves open human MS relevance.
Intracerebral inoculation of Theiler's murine encephalomyelitis virus (TMEV) into susceptible mouse strains results in a chronic, immune-mediated demyelinating disease similar to human multiple sclerosis. Here, we examined the role of astrocytes as an APC population in TMEV-induced demyelination and assessed the potential consequences of T cell activation following Ag presentation. IFN-gamma-pretreated astrocytes were able to process and present all the predominant T cell epitopes of TMEV to virus-specific T cell hybridomas, clones, as well as bulk T cells. Despite low levels of proliferation of T cells due to prostaglandins produced by astrocytes, such Ag presentation by activated astrocytes induced the production of IFN-gamma, a representative proinflammatory cytokine, in TMEV-specific Th cell clones derived from the CNS of virus-infected mice. Furthermore, these Th cell clones mediate lysis of the astrocytes in vitro in a Fas-dependent mechanism. TUNEL staining of CNS tissue demonstrates the presence of apoptotic GFAP+ cells in the white matter of TMEV-infected mice. These results strongly suggest that astrocytes could play an important role in the pathogenesis of TMEV-induced demyelination by activating T cells, subsequently leading to T cell-mediated apoptosis of astrocytes and thereby compromising the blood-brain barrier.
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Palma et al. (1999) studied Theiler's virus-induced demyelination. Intracerebral inoculation of TMEV was evaluated on Role of astrocytes as APCs and T cell-mediated apoptosis of astrocytes. Activated astrocytes present TMEV epitopes to T cells, inducing IFN-gamma production and subsequent Fas-dependent lysis of astrocytes, potentially compromising the blood-brain barrier.
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