Literature DB >> 1533017

Expression of heat shock protein-65 by oligodendrocytes in vivo and in vitro: implications for multiple sclerosis.

K Selmaj1, C F Brosnan, C S Raine.   

Abstract

We studied immunoreactivity for heat shock proteins (HSPs) in multiple sclerosis (MS) brain tissue and detected HSP-65 in chronic MS plaques at the edge of thinly myelinated (or remyelinated) areas. Serial-section immunocytochemistry and double staining revealed that HSP-65+ cells represented reactive, immature oligodendrocytes with strong reactivity for myelin basic protein and weak reactivity for galactocerebroside. Mature oligodendrocytes outside MS plaques did not stain for HSP-65. Control brain sections showed no HSP-65 reactivity. Oligodendrocytes expressed HSP-65 in mixed glial cell cultures. In this system in vitro, oligodendrocytes, but not astrocytes, showed constitutive expression of HSP-65. There was immunoreactivity for HSP-72 in astrocytes in MS and non-MS brains to a similar extent but no association between HSP-72 reactivity and MS plaques. Interestingly, HSP-65+ oligodendrocytes colocalized with T lymphocytes expressing the gamma delta T-cell receptor (TcR). Since HSP-65 has been implicated as a major antigen recognized by TcR gamma delta lymphocytes, our findings might represent a new immunologic interaction within MS plaques that leads to the destruction of immature oligodendrocytes involved in remyelination.

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Year:  1992        PMID: 1533017     DOI: 10.1212/wnl.42.4.795

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  13 in total

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4.  Clonal expansions of activated gamma/delta T cells in recent-onset multiple sclerosis.

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Review 7.  Stress proteins: their role in the normal central nervous system and in disease states, especially multiple sclerosis.

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8.  Hsp70 and its molecular role in nervous system diseases.

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Review 9.  Immunity to heat shock proteins and neurological disorders of women.

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Review 10.  Distinct patterns of multiple sclerosis pathology indicates heterogeneity on pathogenesis.

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