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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
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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.
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Overall design |
Eximination of genes changes in VSMC dedifferentiation
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Contributor(s) |
Wang C, Xu W, Huang K |
Citation missing |
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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
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Organization name |
Massachusetts General Hospital
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Department |
Department of Radiation Oncology
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Lab |
Edwin L. Steele Laboratories
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Street address |
100 Blossom Street
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City |
Boston |
State/province |
Massachusetts |
ZIP/Postal code |
02114 |
Country |
USA |
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Platforms (1) |
GPL14844 |
Illumina HiSeq 2000 (Rattus norvegicus) |
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Samples (6)
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Relations |
BioProject |
PRJNA407927 |
SRA |
SRP118086 |