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Series GSE95546 Query DataSets for GSE95546
Status Public on Mar 14, 2017
Title Integrated analysis of genetic, behavioral, and biochemical data implicates neural stem cell-induced changes in immunity, neurotransmission and mitochondrial function in Dementia with Lewy Body mice
Organism Mus musculus
Experiment type Expression profiling by array
Summary We previously demonstrated that transplantation of murine neural stem cells (NSCs) can improve motor and cognitive function in a transgenic model of Dementia with Lewy Bodies (DLB). The underlying neurobiology that mediates such restoration no doubt involves numerous genes acting in concert to modulate signaling within and between host brain cells and transplanted NSCs. In order to identify functionally connected gene networks and additional mechanisms that may contribute to stem cell-induced benefits, we performed weighted gene co-expression network analysis (WGCNA) on striatal tissue isolated from NSC- and vehicle-injected wild-type and DLB mice. WGCNA is proved to be a powerful approach; revealing significant alterations in immune response, neurotransmission, and mitochondria function in response to NSC treatment.
 
Overall design Age- and sex-matched transgenic mice over-expressing human wild-type alpha-synuclein (PDGF-β-ASO line D, ASO) and wild-type littermates maintained on a congenic C57B6/J background were examined. Hippocampal/cortical GFP-expressing mouse neural stem cells (NSCs) were microdissected from syngeneic GFP-transgenic mice at postnatal day 1 and transplanted at passage 15. Wild-type (WT) and transgenic littermates (ASO) were randomly divided into groups and received intrastriatal injections of either saline (Veh) or haplotype-matched NSCs. The combination of genotype and treatment resulted in four experimental groups: WT-Veh, WT-NSC, ASO-Veh, ASO-NSC. After one month of treatment, all animals were sacrificed and total RNA extracted from microdissected striatum.Then, RNA was processed and subjected to WGCNA analysis.
 
Contributor(s) Lakatos A, Goldberg NR, Blurton-Jones M
Citation(s) 28283027
Submission date Mar 01, 2017
Last update date Feb 21, 2018
Contact name Mathew Blurton-Jones
E-mail(s) mblurton@uci.edu
Phone (949) 824-5243
Organization name University of California, Irvine
Department Department of Neurobiology & Behavior
Street address 3014 Gross Hall
City Irvine
State/province CA
ZIP/Postal code 92627
Country USA
 
Platforms (1)
GPL16570 [MoGene-2_0-st] Affymetrix Mouse Gene 2.0 ST Array [transcript (gene) version]
Samples (20)
GSM2516136 ASO-Veh [1112F-03_CPu_a42]
GSM2516137 ASO-Veh [1112F-03_CPu_a45]
GSM2516138 ASO-Veh [1112F-03_CPu_a46]
Relations
BioProject PRJNA377424

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
GSE95546_RAW.tar 186.2 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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