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Sample GSM2224488 Query DataSets for GSM2224488
Status Public on Dec 06, 2016
Title ConDMSO_day8_rep3
Sample type RNA
Source name PHH_conDMSO_day8
Organism Homo sapiens
Characteristics cell type, study type, assay type, strain, compound, dose, dose unit, dose duration, duration unit, dose frequency: primary human hepatocytes
assay type: in vitro
study type: single dose toxicity
strain: Hu8119+Hu1591+Hu1540
dose: DMSO 0.5 %
dose duration: 8 days
Treatment protocol After quick thawing in a water bath at 37°C, viability of the cells was checked by a Trypan blue (CAS no. 72-57-1, Sigma–Aldrich) exclusion test as instructed in the supplier’s protocol (Invitrogen, 2012). All viability scores after thawing were in agreement with those listed by the supplier. Before CsA treatment, cells were allowed to acclimatize for 48 hours. This is needed for the hepatocytes to restore an in vivo like cellular configuration and enzyme expression levels as optimally as possible. PHH were treated with 30 µM CsA for 5 days daily followed by a washout-period (terminating CsA-treatment) of 3 days.
Growth protocol Cryopreserved primary human hepatocytes (PHH) were purchased from Life Technologies. Cells were cultured in pre-coated 24-well plates (2,100,000 cells/sample) in a 2-layer collagen sandwich (A11428-02, Gibco), according to the supplier’s protocol (Invitrogen, 2012). The following culture media were used: Hepatocyte Thawing Medium (HTM) for thawing (CM7500, Gibco), Williams’ Medium E (1x, no phenol red) (A1217601, Gibco) + Cell Maintenance supplement B kit (CM4000, Gibco) for plating and incubation.
Extracted molecule total RNA
Extraction protocol Cells were cultured in triplicate in 24 wells in a collagen sandwich layer. Following 5 days of repetitive daily exposureand thereupon a washout of 3 days, cells lysates were harvested for total RNA isolation after 3, 5 and 8 days. Therefore, medium was removed and PHH were harvested in Qiazol (Qiagen). Total RNA was isolated using a miRNeasy Mini Kit (Qiagen) according to the manufacturer’s protocol and followed by DNase I (Qiagen) treatment. Upon purification, RNA concentrations were measured by means of a NanoDrop® ND-1000 spectrophotometer (Thermo Scientific) at 260 and 280 nm. RNA quality and integrity were assessed by using automated gel electrophoresis on an Agilent 2100 Bioanalyzer system (Agilent Technologies). Only RNA samples which showed clear 18S and 28S peaks and with an RNA integrity number (RIN) higher than 6, were used. Samples were stored at -80ºC until RNA hybridization.
Label biotin
Label protocol High-density oligonucleotide GeneChips from Affymetrix were used to measure gene expression levels (Human Genome U133 Plus 2.0 array (604,258 probes)). Targets for these arrays were prepared, hybridized and scanned according to the Affymetrix protocol (Affymetrix).Normalization quality controls appeared to be within acceptable limits for almost all chips.
Hybridization protocol Amplified, biotinylated and fragmented targets were then hybridized on to the BrainArray custom CDF v15.1.0 array.
Scan protocol After hybridization, arrays were washed and stained using an Affymetrix fluidics station and scanned by use of an Affymetrix GeneArray scanner. A total of 60 RNA samples was prepared and analyzed on GeneChip arrays (treated and control samples from each time point were at least in triplicate). Normalization quality controls, including scaling factors, average intensities, present calls, background intensities, noise, and raw Q values, appeared to be within acceptable limits for all chips. Hybridization controls BioB, BioC, BioD, and CreX were called present on all chips and yielded the expected increases in intensities.
Data processing The web service was used for quality control (27) and all microarrays were of high quality. CEL files were imported into R v2.15.3 ( using the “affy” library (28) within BioConductor (v2.9) (29). Probe re-annotation, normalization and data filtering was performed as previously described (30).
Submission date Jul 01, 2016
Last update date Dec 06, 2016
Contact name Jarno Wolters
Organization name Maastricht University
Department Toxicogenomics
Street address Universiteitssingel 40
City Maastricht
ZIP/Postal code PO BOX 616/ 6200MD
Country Netherlands
Platform ID GPL17996
Series (2)
GSE83958 Integrative "-omics" analysis in primary human hepatocytes unravels persistent mechanisms of cyclosporine A-induced cholestasis (RNA)
GSE84281 Integrative "-omics" analysis in primary human hepatocytes unravels persistent mechanisms of cyclosporine A-induced cholestasis

Data table header descriptions
VALUE RMA normalized intensity signals

Data table
1_at 6.992353622
10_at 10.92736732
100_at 6.964740049
1000_at 11.56765578
100009676_at 6.042465897
10001_at 9.249364343
100049716_at 7.29359193
10005_at 8.930673526
10006_at 10.67173214
10007_at 10.51565831
10009_at 10.66590005
100093630_at 11.03436117
1001_at 6.393559404
10010_at 9.633026579
100101467_at 7.660441982
10011_at 10.08649516
100113407_at 7.777055215
100125288_at 6.976562552
100126784_at 6.288195836

Total number of rows: 12738

Table truncated, full table size 253 Kbytes.

Supplementary file Size Download File type/resource
GSM2224488_Sample_15_DNA-3co-8d_HG-U133_Plus_2_.CEL.gz 4.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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