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10.1186/s12974-017-0879-5

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suck abstract from ncbi


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pmid28532450
      J+Neuroinflammation 2017 ; 14 (1 ): 106
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  • LPS-induced systemic inflammation reveals an immunomodulatory role for the prion protein at the blood-brain interface #MMPMID28532450
  • Salvesen Ø ; Reiten MR ; Espenes A ; Bakkebø MK ; Tranulis MA ; Ersdal C
  • J Neuroinflammation 2017[May]; 14 (1 ): 106 PMID28532450 show ga
  • BACKGROUND: The cellular prion protein (PrP(C)) is an evolutionary conserved protein abundantly expressed not only in the central nervous system but also peripherally including the immune system. A line of Norwegian dairy goats naturally devoid of PrP(C) (PRNP (Ter/Ter)) provides a novel model for studying PrP(C) physiology. METHODS: In order to explore putative roles for PrP(C) in acute inflammatory responses, we performed a lipopolysaccharide (LPS, Escherichia coli O26:B6) challenge of 16 goats (8 PRNP (+/+) and 8 PRNP (Ter/Ter)) and included 10 saline-treated controls (5 of each PRNP genotype). Clinical examinations were performed continuously, and blood samples were collected throughout the trial. Genome-wide transcription profiles of the choroid plexus, which is at the blood-brain interface, and the hippocampus were analyzed by RNA sequencing, and the same tissues were histologically evaluated. RESULTS: All LPS-treated goats displayed clinical signs of sickness behavior, which were of significantly (p?
  • |Animals [MESH]
  • |Animals, Genetically Modified [MESH]
  • |Brain/*metabolism [MESH]
  • |Calcium-Binding Proteins [MESH]
  • |Choroid Plexus/metabolism/pathology [MESH]
  • |Chromatin Immunoprecipitation [MESH]
  • |Cytokines/metabolism [MESH]
  • |DNA-Binding Proteins/metabolism [MESH]
  • |Disease Models, Animal [MESH]
  • |Gene Expression Profiling [MESH]
  • |Gene Expression Regulation/drug effects/genetics [MESH]
  • |Gene Ontology [MESH]
  • |Genotype [MESH]
  • |Goats [MESH]
  • |Illness Behavior/drug effects/physiology [MESH]
  • |Immunity, Innate/drug effects [MESH]
  • |Inflammation/*blood/chemically induced/*immunology/*pathology [MESH]
  • |Lipopolysaccharides/toxicity [MESH]
  • |Microfilament Proteins [MESH]
  • |Prion Proteins/blood/genetics/*metabolism [MESH]
  • |RNA, Messenger/metabolism [MESH]


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