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Sample GSM6043357 Query DataSets for GSM6043357
Status Public on Apr 14, 2022
Title HepaRG cells treated with SM-VD2 and OA/PA 3
Sample type RNA
 
Source name Treated with William E complete medium with a mix of oleic acid [200 µM] and palmitic acid [200 µM]+vitamin D2-containing extract derived from Shitake mushroom [10 nM]
Organism Homo sapiens
Characteristics cell line: hepatic cell line
features: Immortalized hepatic cell line terminally differentiated
age: Adult
Treatment protocol At 70% confluence, HepaRG cells were incubated for 24 hrs with either the vehicle or the three different sources of Vitamin D at final concentration of α-Tocopherol in the colture medium of 10 nM. Subsequently HepaRG were incubated with OA/PA mix at the final concentration in the colture medium of 200 µM. Cell treatments with this OA/PA lasted for 48 hrs.
Growth protocol Cells were seeded at a density of 10,000 cells/well and kept at 37˚C in a humidified 5% CO2 cell culture incubator.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from cells lysates using an QIAsymphony RNA Kit (Qiagen,) with the QIAsymphony SP instrument (Qiagen) according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA was prepared according to the standard ThermoFisher Scientific protocol from 6 ug total RNA (GeneChip™ 3’ IVT Pico Kit Manual Workflow).
 
Hybridization protocol Fragmented and labeled cDNA was prepared according to the manufacturer's instructions and hybridized to a Human Clariom Go Screen 384-array plate for 17 h at 45°C on a GeneTitan MC Instrument (Applied Biosystems, ThermoFisher Scientific). Arrays were washed and stained on a GeneTitan MC Instrument (Applied Biosystems, ThermoFisher Scientific).
Scan protocol Arrays were scanned using the GeneTitan MC Instrument (Applied Biosystems, ThermoFisher Scientific). Affymetrix GeneChip Command Console Software (AGCC, ThermoFisher Scientific) was used for GeneTitan MC Instrument control.
Data processing Data analysis were performed using Transcriptomic Analysis Console Software (TAC, ThermoFisher Scientific) that provides quality control analysis, performs normalization and summarization, based on the Signal Space Transformation-Robust Multi-Chip Analysis (SST-RMA) analysis algorithm, and provides a list of differentially expressed genes (Limma Bioconductor package, pvalue<0,05) from the biological duplicates for WGO-VE_OA or triplicates of the other condition.
 
Submission date Apr 13, 2022
Last update date Apr 14, 2022
Contact name Jacopo Lucci
E-mail(s) jlucci@biostherapy.it
Phone +393428018168
Organization name Bios-Therapy, Physiological Systems For Health S.p.A
Lab Laboratory of system biology
Street address Loc. Aboca, 20
City Sansepolcro
State/province Arezzo
ZIP/Postal code 52037
Country Italy
 
Platform ID GPL31262
Series (1)
GSE200765 Vitamin D cytoprotection function in human liver cell lipotoxicity and its transcriptomic fingerprint: a comparison of natural and synthetic formulations.

Data table header descriptions
ID_REF
VALUE The data in the matrix table contains the Gene level SST-RMA.

Data table
ID_REF VALUE
Zika_virus__gi_226377833.vir.1 3.69
TCUn_GL000219v100006438.hg.2 11.15
TCUn_GL000218v100006433.hg.2 11.05
TCUn_GL000195v100006435.hg.2 6.61
TC6_GL000254v2_alt00006744.hg.2 10.85
TC6_GL000250v2_alt00006607.hg.2 6.68
TC2200009366.hg.2 4.86
TC2200009365.hg.2 10.49
TC2200009364.hg.2 5.73
TC2200009363.hg.2 5.7
TC2200009362.hg.2 10.51
TC2200009361.hg.2 7.42
TC2200009360.hg.2 8.91
TC2200009357.hg.2 12.67
TC2200009356.hg.2 12.83
TC2200009355.hg.2 7.92
TC2200009353.hg.2 10.61
TC2200009352.hg.2 11.39
TC2200009351.hg.2 13.1
TC2200009350.hg.2 12.08

Total number of rows: 19978

Table truncated, full table size 453 Kbytes.




Supplementary file Size Download File type/resource
GSM6043357_B24_SM-VD2_OAPA_3.CEL.gz 424.0 Kb (ftp)(http) CEL
Processed data included within Sample table

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