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Series GSE103995 Query DataSets for GSE103995
Status Public on Sep 20, 2018
Title PARP1 regulates VSMC phenotypic switch and neointima via Myocardin
Organism Rattus norvegicus
Experiment type Expression profiling by high throughput sequencing
Summary We applied the transcriptome profiling (RNA-seq) for high-throughput profiling of genes changes in VSMC dedifferentiation. Rat primary VSMCs were divided into 3 groups, control, PDGF-BB, PDGF-BB+PJ34,and mRNA sequence were performed. We found that PDGF-BB could upregualted the genes involved in cell proliferation and migration, and downregulated the VSMC contractile genes, all of which could be reversed by PARP inhibitor PJ34. Then we knockdowned the co-factor Myocardin in VSMCs, and found the above effects of PJ34 were nearly abolished.Our study first provided the transcription changes by RNA-seq in VSMC dedifferentiation, and demonstrated the key roles of PARP1 and the PARylation process in VSMC phenotypic switch.
 
Overall design Eximination of genes changes in VSMC dedifferentiation
 
Contributor(s) Wang C, Xu W, Huang K
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Submission date Sep 19, 2017
Last update date Jul 25, 2021
Contact name Pin-Ji Lei
E-mail(s) leipinji@gmail.com
Organization name Massachusetts General Hospital
Department Department of Radiation Oncology
Lab Edwin L. Steele Laboratories
Street address 100 Blossom Street
City Boston
State/province Massachusetts
ZIP/Postal code 02114
Country USA
 
Platforms (1)
GPL14844 Illumina HiSeq 2000 (Rattus norvegicus)
Samples (6)
GSM2787507 control
GSM2787508 BB
GSM2787509 BB+PJ34
Relations
BioProject PRJNA407927
SRA SRP118086

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
GSE103995_RAW.tar 610.0 Kb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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