Literature DB >> 21221923

PrP 106-126 altered PrP mRNA gene expression in mouse microglia BV-2 cells.

Yu Bai1, Yu-rong Li, Gui-hua Wang, Xiang-mei Zhou, De-ming Zhao.   

Abstract

Prion diseases are infectious and fatal neurodegenerative diseases. The pathogenic agent is an abnormal prion protein aggregate. Microglial activation in the centre nervous system is a characteristic feature of prion disease. In this study, we examined the effect of PrP 106-126 on PrP mRNA gene expression in Mouse microglia cells BV-2 by real-time quantitative PCR. PrP mRNA expression level was found to be significantly increased after 18 h exposure of BV-2 cells to PrP 106-126, with 3-fold increase after 18 h and 4.5-fold increase after 24 h and BV-2 cells proliferating occurred correspondingly. Our results provide the first in vitro evidence of the increase of PrP mRNA levels in microglial cells exposed to PrP 106-126, and indicate that microglial cells might play a critical role in prion pathogenesis.

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Year:  2011        PMID: 21221923      PMCID: PMC8227900          DOI: 10.1007/s12250-010-3143-z

Source DB:  PubMed          Journal:  Virol Sin        ISSN: 1995-820X            Impact factor:   4.327


  21 in total

Review 1.  Shattuck lecture--neurodegenerative diseases and prions.

Authors:  S B Prusiner
Journal:  N Engl J Med       Date:  2001-05-17       Impact factor: 91.245

2.  Cellular uptake of the prion protein fragment PrP106-126 in vitro.

Authors:  S J McHattie; D R Brown; M M Bird
Journal:  J Neurocytol       Date:  1999-02

3.  Microglial activation varies in different models of Creutzfeldt-Jakob disease.

Authors:  C A Baker; Z Y Lu; I Zaitsev; L Manuelidis
Journal:  J Virol       Date:  1999-06       Impact factor: 5.103

4.  Mice devoid of PrP are resistant to scrapie.

Authors:  H Büeler; A Aguzzi; A Sailer; R A Greiner; P Autenried; M Aguet; C Weissmann
Journal:  Cell       Date:  1993-07-02       Impact factor: 41.582

5.  Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.

Authors:  F Tagliavini; F Prelli; L Verga; G Giaccone; R Sarma; P Gorevic; B Ghetti; F Passerini; E Ghibaudi; G Forloni
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

6.  Developmental expression of the prion protein gene in glial cells.

Authors:  M Moser; R J Colello; U Pott; B Oesch
Journal:  Neuron       Date:  1995-03       Impact factor: 17.173

7.  Neurotoxicity of a prion protein fragment.

Authors:  G Forloni; N Angeretti; R Chiesa; E Monzani; M Salmona; O Bugiani; F Tagliavini
Journal:  Nature       Date:  1993-04-08       Impact factor: 49.962

8.  Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.

Authors:  M Barcikowska; P P Liberski; J W Boellaard; P Brown; D C Gajdusek; H Budka
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

Review 9.  Prions.

Authors:  S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-10       Impact factor: 11.205

10.  Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.

Authors:  S B Prusiner; D Groth; A Serban; R Koehler; D Foster; M Torchia; D Burton; S L Yang; S J DeArmond
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-15       Impact factor: 11.205

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  1 in total

Review 1.  Microglia in Prion Diseases: Angels or Demons?

Authors:  Caterina Peggion; Roberto Stella; Paolo Lorenzon; Enzo Spisni; Alessandro Bertoli; Maria Lina Massimino
Journal:  Int J Mol Sci       Date:  2020-10-20       Impact factor: 5.923

  1 in total

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