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Status |
Public on Dec 08, 2021 |
Title |
hiPSC-CM control A1 |
Sample type |
SRA |
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Source name |
Induced Pluripotent Stem Cell derived cardiomyocytes
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Organism |
Homo sapiens |
Characteristics |
cell line: iCell cardiomyocytes (Cellular Dynamics) treatment: EtOH 0.01% for 24 hours
|
Treatment protocol |
The day before treatment, the cells were fed with serum-free (BMCC) medium. The specific culture media were completely replaced with fresh media prior to compound addition and after four hours of stabilization at 5% CO2 and at 37 °C, cells were treated by adding a 1:10 dilution of each 10x compound working solutions. The final compound concentrations used were 0.01% EtOH and 1 nM T3. Total RNA was extracted 24h after treatments.
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Growth protocol |
The cardiomyocytes were thawed in iCell Cardiomyocytes Plating Medium and directly plated onto fibronectin-coated CytoView MEA 48 wells white plates (Axion Biosystem, Atlanta, GA, USA) at 3x104 plated viable cells per well, based on lot specific plating efficiency. The hiPSC-CMs were incubated at 37 °C with 5% CO2 and allowed to attach for 2 h in moisturized conditions, prior filling each well with 0.3 mL of Plating medium. On day 2 post-plating, the spent medium was replaced with iCell Maintenance (iCM) medium and thereafter 50% of the medium was replaced every 2-3 days, up to cells treatment. Before the experiments, hiPSC-CMs were cultured for four weeks after plating to improve their functional maturation.
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was isolated using total RNA mini kit (Norgen Biotech Corp.) following manufacturer’s instructions. RNA libraries were prepared Ion AmpliSeq™ Transcriptome Human Gene Expression Kit (following Ion Torrent user guide, Publication Number MAN0010742 ); for sequencing was usde Ion 540™ Kit – Chef (following Ion Torrent user guide, Publication Number MAN0010851)
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Ion Torrent S5 |
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Description |
Sample A1 Data_Matrix_AvsB.xlsx Filtered_Normalized_Data_AvsB.xlsx Differential_Expression_AvsB.xlsx GO_BP_Functional_Analysis_AvsB.xlsx
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Data processing |
The reads were mapped and analyzed with the Torrent Suite (version 5.12.1). AmpliseqRNA plugin (version 5.12.0.1) was used to map the sequencing reads on Target Regions. Reference Library: hg19_ampliseq_transcriptome_ercc_v1(hg19 AmpliSeq Transcriptome ERCC v1) Target Regions: hg19_AmpliSeq_Transcriptome_21K_v1.bed Genome_build: hg19 AmpliSeq Transcriptome ERCC v1 Normalization method CPM (counts per million): counts scaled by total number of reads The differential analysis was carried out with the R package edgeR Supplementary_files_format_and_content: Data matrix Supplementary_files_format_and_content: Filtered Normalized Data Supplementary_files_format_and_content: Differential Expression Supplementary_files_format_and_content: GO.BP functional analysis
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Submission date |
Apr 19, 2021 |
Last update date |
Dec 08, 2021 |
Contact name |
Alessandra Ulivieri |
Organization name |
Niccolò Cusano University Foundation
|
Department |
Laboratory of Biomedical Research
|
Street address |
Via Don Carlo Gnocchi 3
|
City |
Rome |
ZIP/Postal code |
00166 |
Country |
Italy |
|
|
Platform ID |
GPL23934 |
Series (1) |
GSE172348 |
Thyroid Hormone effects on hiPSC-derived cardiomyocytes (hiPSC-CM). Identification of target genes and pathways by RNA-Seq analysis |
|
Relations |
BioSample |
SAMN18796895 |
SRA |
SRX10636230 |