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. 1991 Nov;65(11):6292–6295. doi: 10.1128/jvi.65.11.6292-6295.1991

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease.

T Kitamoto 1, T Muramoto 1, S Mohri 1, K Doh-Ura 1, J Tateishi 1
PMCID: PMC250334  PMID: 1681118

Abstract

We established that follicular dendritic cells (FDCs) are the site of abnormal prion protein (PrPCJD) accumulations in lymphoid tissues from mice infected with Creutzfeldt-Jakob disease. Evidence of positive FDC staining was observed in Creutzfeldt-Jakob disease-infected mice irrespective of the inoculation route, while no such staining was seen in the control mice. We also found that the severe combined immunodeficiency mouse trait is transmittable via the intracranial route but not via the intraperitoneal route. Mice with severe combined immunodeficiency did not have PrPCJD accumulation in FDCs.

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Selected References

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