Literature DB >> 11201083

Early loss of dendritic spines in murine scrapie revealed by confocal analysis.

D Brown1, P Belichenko, J Sales, M Jeffrey, J R Fraser.   

Abstract

Confocal analysis of dye-filled neurons has revealed a significant early loss of dendritic spines in a murine scrapie model in which neuron loss occurs in the hippocampus. An 18% loss of spines was found at 109 days, > 50 days before neuron loss occurs, and by 126 days a 51% spine loss was found. Spine loss is concurrent with synapse loss, axon terminal degeneration and a decrease in long term potentiation in this model. Preceding these changes is the deposition of disease specific PrP at 70 days, which may initiate the damage to dendritic spines and the subsequent degeneration of synapses. We suggest that these changes underlie the development of clinical disease in the transmissible spongiform encephalopathies.

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Year:  2001        PMID: 11201083     DOI: 10.1097/00001756-200101220-00043

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  13 in total

1.  Highly neurotoxic monomeric α-helical prion protein.

Authors:  Minghai Zhou; Gregory Ottenberg; Gian Franco Sferrazza; Corinne Ida Lasmézas
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-07       Impact factor: 11.205

2.  Degenerating synaptic boutons in prion disease: microglia activation without synaptic stripping.

Authors:  Zuzana Sisková; Anton Page; Vincent O'Connor; Victor Hugh Perry
Journal:  Am J Pathol       Date:  2009-09-24       Impact factor: 4.307

3.  Plasma membrane invaginations containing clusters of full-length PrPSc are an early form of prion-associated neuropathology in vivo.

Authors:  Susan F Godsave; Holger Wille; Jason Pierson; Stanley B Prusiner; Peter J Peters
Journal:  Neurobiol Aging       Date:  2013-06       Impact factor: 4.673

4.  Dendritic pathology in prion disease starts at the synaptic spine.

Authors:  Martin Fuhrmann; Gerda Mitteregger; Hans Kretzschmar; Jochen Herms
Journal:  J Neurosci       Date:  2007-06-06       Impact factor: 6.167

5.  Early mechanisms of pathobiology are revealed by transcriptional temporal dynamics in hippocampal CA1 neurons of prion infected mice.

Authors:  Anna Majer; Sarah J Medina; Yulian Niu; Bernard Abrenica; Kathy J Manguiat; Kathy L Frost; Clark S Philipson; Debra L Sorensen; Stephanie A Booth
Journal:  PLoS Pathog       Date:  2012-11-08       Impact factor: 6.823

6.  Early increase and late decrease of purkinje cell dendritic spine density in prion-infected organotypic mouse cerebellar cultures.

Authors:  Jody L Campeau; Gengshu Wu; John R Bell; Jay Rasmussen; Valerie L Sim
Journal:  PLoS One       Date:  2013-12-02       Impact factor: 3.240

7.  Differential protein profiling as a potential multi-marker approach for TSE diagnosis.

Authors:  Janice B Barr; Michael Watson; Mark W Head; James W Ironside; Nathan Harris; Caroline Hogarth; Janet R Fraser; Rona Barron
Journal:  BMC Infect Dis       Date:  2009-11-27       Impact factor: 3.090

8.  The CNS glycoprotein Shadoo has PrP(C)-like protective properties and displays reduced levels in prion infections.

Authors:  Joel C Watts; Bettina Drisaldi; Vivian Ng; Jing Yang; Bob Strome; Patrick Horne; Man-Sun Sy; Larry Yoong; Rebecca Young; Peter Mastrangelo; Catherine Bergeron; Paul E Fraser; George A Carlson; Howard T J Mount; Gerold Schmitt-Ulms; David Westaway
Journal:  EMBO J       Date:  2007-08-16       Impact factor: 11.598

Review 9.  Synaptic dysfunction in prion diseases: a trafficking problem?

Authors:  Assunta Senatore; Elena Restelli; Roberto Chiesa
Journal:  Int J Cell Biol       Date:  2013-11-28

10.  T-Tau and P-Tau in Brain and Blood from Natural and Experimental Prion Diseases.

Authors:  Richard Rubenstein; Binggong Chang; Robert Petersen; Allen Chiu; Peter Davies
Journal:  PLoS One       Date:  2015-12-02       Impact factor: 3.240

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