Back to Search
Start Over
Identification of genes differentially expressed in SH-SY5Y neuroblastoma cells exposed to the prion peptide 106-126.
- Source :
-
The European journal of neuroscience [Eur J Neurosci] 2007 Jul; Vol. 26 (1), pp. 51-9. Date of Electronic Publication: 2007 Jun 26. - Publication Year :
- 2007
-
Abstract
- Prion diseases are a group of neurodegenerative disorders characterized by astrocytosis and progressive neuronal degeneration. As a causative agent, prions have been intensely investigated in different experimental models. However, the mechanisms and pathways involved in the prion-induced neurological dysfunction are poorly understood. In this work we have investigated the influence of prion infection on the gene expression profile in a human neuroblastoma cell line. Using a DNA microarray and quantitative reverse transcriptase-polymerase chain reaction methods, we have analysed in SH-SY5Y cells the effects of a synthetic peptide corresponding to the 106-126 neurotoxic region of the cellular human prion protein. Our results show that addition of this peptide to the neuronal culture specifically changes the expression of a relative high number of genes, and causes a progressive neuronal death even in the absence of microglia.
- Subjects :
- Cell Death physiology
Cell Line, Tumor
Down-Regulation genetics
Down-Regulation physiology
Humans
Microscopy, Fluorescence
Neuroglia drug effects
Neuroglia metabolism
Oligonucleotide Array Sequence Analysis
Prions genetics
RNA biosynthesis
RNA genetics
Reverse Transcriptase Polymerase Chain Reaction
Tetrazolium Salts
Thiazoles
Transcription, Genetic
Gene Expression physiology
Neuroblastoma genetics
Neuroblastoma metabolism
Peptide Fragments pharmacology
Prions pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0953-816X
- Volume :
- 26
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The European journal of neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 17596192
- Full Text :
- https://doi.org/10.1111/j.1460-9568.2007.05646.x