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Series GSE85952 Query DataSets for GSE85952
Status Public on Aug 24, 2016
Title Design, characterization, and use of a novel amyloid β-protein control for assembly, neurotoxicity, and gene expression studies
Organism Rattus norvegicus
Experiment type Expression profiling by array
Summary A key pathogenic agent in Alzheimer’s disease (AD) is the amyloid β-protein (Aβ), which self-assembles into a variety of neurotoxic structures. Establishing structure-activity relationships for these assemblies is critical for proper therapeutic target identification and design. We examined the effects of Aβ monomers, dimers, higher-order oligomers, and fibrils on gene expression in primary rat hippocampal neurons. As opposed to “reverse” Aβ or non-Aβ peptides typically used as controls in such studies, we designed novel scrambled Aβ peptides predicted to behave distinctly from native Aβ. Significant changes in gene expression were observed for all peptide assemblies, but fibrils induced the largest changes. Significant changes in gene expression were observed for all peptide assemblies, but fibrils induced the largest changes. Weighted gene co-expression network analysis (WGCNA) revealed two predominant gene modules related to Aβ treatment. Many genes within these modules were associated with inflammatory signaling pathways
 
Overall design We examined the effects of Aβ monomers, dimers, higher-order oligomers, and fibrils on gene expression in primary rat hippocampal neurons. Novel scrambled Aβ peptides, as opposed to “reverse” Aβ or non-Aβ peptides, were used as controls.

Please note that the 'XL42_1' sample was excluded from data processing as an outlier (resulting total 23 sample records). However the 'XL42_1' raw data is provided in the 'non_normalized.txt' (total 24 data columns).
 
Contributor(s) Yamin G, Coppola G, Teplow DB
Citation(s) 27505174
NIH grant(s)
Grant ID Grant title Affiliation Name
P30 NS062691 Informatics Center for Neurogenetics and Neurogenomics: Integrative Center for Neurogenetics and Neurogenomics - Overall UNIVERSITY OF CALIFORNIA LOS ANGELES Nelson B Freimer
Submission date Aug 23, 2016
Last update date Nov 23, 2016
Contact name Giovanni Coppola
E-mail(s) gcoppola@ucla.edu
Phone 310-794-4172
Organization name UCLA
Department Psychiatry and Neurology
Lab Neurogenetics
Street address 1524 Gonda, 695 Charles Young Drive South
City Los Angeles
State/province CA
ZIP/Postal code 90095
Country USA
 
Platforms (1)
GPL6101 Illumina ratRef-12 v1.0 expression beadchip
Samples (23)
GSM2288385 cont_1
GSM2288386 cont_2
GSM2288387 cont_3
Relations
BioProject PRJNA339827

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE85952_RAW.tar 2.8 Mb (http)(custom) TAR
GSE85952_non_normalized.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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