PrP Deposition, Microglial Activation, and Neuronal Apoptosis in Murine Scrapie

The present study investigated the relationship among PrP deposition, microglial activation, vacuolation, and neuronal death in the hippocampus of the 301V/VM murine scrapie model (mean incubation period 117 +/- 1 days). PrP deposition was first detected after 30 days and microglial activation after 60 days. Vacuolation in the CA1 and CA2 pyramidal layer was present from 90 days onward. Only occasional in situ end labeling (ISEL)-positive neurons were present in the hippocampus of scrapie-infected mice from 75 days postinoculation (d.p.i.), except at 105 d.p.i. when relatively large numbers of apoptotic, ISEL-positive neurons in the CA1 hippocampal region were observed. Terminally ill animals showed almost complete loss of CA1 pyramidal neurons. Electron microscopy of the CA1 region at 105 days confirmed that these neurons were dying by apoptosis. These data suggest that microglial activation in scrapie is a response to abnormal PrP deposition rather than a response to neuronal cell loss.

[1]  R. Sidman,et al.  Atlas of the Mouse Brain and Spinal Cord , 1971 .

[2]  S. Whatley,et al.  Regulation of intracellular free calcium levels by the cellular prion protein. , 1995, Neuroreport.

[3]  H. Fraser,et al.  RETINOPATHY IN MICE WITH EXPERIMENTAL SCRAPIE , 1986, Neuropathology and applied neurobiology.

[4]  N. C. Price,et al.  Cytotoxicity of prion protein peptide (PrP106-126) differs in mechanism from the cytotoxic activity of the Alzheimer's disease amyloid peptide, A beta 25-35. , 1996, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.

[5]  A. Wyllie,et al.  Cell death: the significance of apoptosis. , 1980, International review of cytology.

[6]  M. Jeffrey,et al.  Morphogenesis of amyloid plaques in 87V murine scrapie † , 1994, Neuropathology and applied neurobiology.

[7]  H. Fraser,et al.  Detection of apoptosis in murine scrapie , 1995, Neuroscience Letters.

[8]  S. Prusiner,et al.  Scrapie prions alter receptor‐mediated calcium responses in cultured cells , 1993, Neurology.

[9]  C. Masters,et al.  Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change. , 1978, Brain : a journal of neurology.

[10]  H. Fraser,et al.  Scrapie in mice. Agent-strain differences in the distribution and intensity of grey matter vacuolation. , 1973, Journal of comparative pathology.

[11]  M. Jeffrey,et al.  Early unsuspected neuron and axon terminal loss in scra pie‐infected mice revealed by morphometry and immunocytochemistry , 1995, Neuropathology and applied neurobiology.

[12]  H. Ushijima,et al.  Cytoprotective effect of NMDA receptor antagonists on prion protein (PrionSc)-induced toxicity in rat cortical cell cultures. , 1993, European journal of pharmacology.

[13]  Bernhard Schmidt,et al.  Role of microglia and host prion protein in neurotoxicity of a prion protein fragment , 1996, Nature.

[14]  R. Anadón,et al.  Ganglion cells and retinopetal fibers of the larval lamprey retina: An HRP ultrastructural study , 1989, Neuroscience Letters.

[15]  M. Jeffrey,et al.  Murine scrapie-infected neurons in vivo release excess prion protein into the extracellular space , 1994, Neuroscience Letters.

[16]  V. Perry,et al.  Characterization of the microglial response in murine scrapie , 1994, Neuropathology and applied neurobiology.

[17]  C. Kurschner,et al.  The cellular prion protein (PrP) selectively binds to Bcl-2 in the yeast two-hybrid system. , 1995, Brain research. Molecular brain research.

[18]  S. Ben‐Sasson,et al.  Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation , 1992, The Journal of cell biology.

[19]  M. Jeffrey,et al.  Correlative light and electron microscopy studies of PrP localisation in 87V scrapie , 1994, Brain Research.

[20]  A. Giese,et al.  Neuronal Cell Death in Scrapie‐Infected Mice Is Due to Apoptosis , 1995, Brain pathology.

[21]  I. W. Mclean,et al.  PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY , 1974, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[22]  R J Fletterick,et al.  Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[23]  G. Forloni,et al.  Neurotoxicity of a prion protein fragment , 1993, Nature.

[24]  S. Prusiner,et al.  Changes in the localization of brain prion proteins during scrapie infection , 1998, Neurology.

[25]  A. Aguzzi,et al.  Normal host prion protein necessary for scrapie-induced neurotoxicity , 1996, Nature.

[26]  V. Perry,et al.  Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain , 1990, Neuroscience.

[27]  G. Kinney Peripheral nicotine administration increases rubral firing rates in the urethane-anesthetized rat , 1995, Neuroscience Letters.

[28]  M. van Lookeren Campagne,et al.  Microwave-enhanced in situ end-labeling of fragmented DNA: parametric studies in relation to postmortem delay and fixation of rat and human brain. , 1995, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[29]  J. H. Dierendonck,et al.  A new method to detect apoptosis in paraffin sections: in situ end-labeling of fragmented DNA. , 1993, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[30]  H. Kretzschmar,et al.  Mouse cortical cells lacking cellular PrP survive in culture with a neurotoxic PrP fragment , 1994, Neuroreport.