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Sample GSM3580451 Query DataSets for GSM3580451
Status Public on Dec 31, 2019
Title THP-1_E_Control HDE
Sample type RNA
 
Source name THP-1 monocytes
Organism Homo sapiens
Characteristics cell line: THP-1
hepatocyte donor id: E
treatment: Control HDE
Treatment protocol Exposures were conducted in 96-well round-bottom plates (Corning) at a density of 1 x 10^5 cells per well. THP-1 monocytes were exposed to 200 µg/ml HDE or the matched volume of mock in separate experiments for each hepatocyte donor.
Growth protocol THP-1 human monocytes (TIB-202, ATCC) were cultured in suspension in RPMI-1640 (ATCC) supplemented with 10% (v/v) Exosome-Depleted FBS (Gibco), penicillin-streptomycin (Gibco), and 0.05 mM β-mercaptoethanol (Sigma).
Extracted molecule total RNA
Extraction protocol Cells were lysed in QIAzol (Qiagen) and isolated using the miRNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions.
Label biotin
Label protocol Following purification, 5.5 µg of ss-cDNA were fragmented and end labeled with biotin before hybridizing to the array plate
 
Hybridization protocol GeneTitan robotic instrumentation was used to perform the hybridization, washing, and scanning of the peg array using the Affymetrix GeneTitan Hybridization, Wash, and Stain Kit for WT Arrays.
Scan protocol GeneTitan robotic instrumentation was used to perform the hybridization, washing, and scanning of the peg array using the Affymetrix GeneTitan Hybridization, Wash, and Stain Kit for WT Arrays.
Description THP-1 RNA
Data processing Affymetrix CEL files were normalized using Robust Multi-array Average (RMA) method with a log base 2 (log2) transformation (Irizarry et al., 2003). Principal component analysis (PCA) was used to evaluate the overall performance of the arrays and identify outliers. A filtering step was performed to remove low expression probe sets. Gene expression differences were identified using ANOVA models with linear contrasts.
 
Submission date Jan 25, 2019
Last update date Jan 01, 2020
Contact name Merrie Mosedale
Organization name UNC Eshelman School of Pharmacy
Department Division of Pharmacotherapy and Experimental Therapeutics
Lab Institute for Drug Safety Sciences
Street address 301 Pharmacy Lane, Kerr Hall CB#7569
City Chapel Hill
State/province North Carolina
ZIP/Postal code 27599
Country USA
 
Platform ID GPL24324
Series (1)
GSE125690 Gene expression data from THP-1 cells exposed to exosomes from acetaminophen-treated or vehicle-treated hepatocytes or corresponding mock- or medium-controls

Data table header descriptions
ID_REF
VALUE RMA transformed data processed as described above.

Data table
ID_REF VALUE
TC0100006479.hg.1 6.7829
TC0100006480.hg.1 4.88931
TC0100006483.hg.1 5.0618
TC0100006486.hg.1 6.18206
TC0100006494.hg.1 7.49161
TC0100006497.hg.1 3.83743
TC0100006499.hg.1 6.7157
TC0100006501.hg.1 6.52452
TC0100006524.hg.1 6.08956
TC0100006550.hg.1 5.76178
TC0100006565.hg.1 7.52827
TC0100006571.hg.1 4.89985
TC0100006577.hg.1 9.50358
TC0100006587.hg.1 5.9291
TC0100006613.hg.1 4.05573
TC0100006619.hg.1 7.53493
TC0100006620.hg.1 6.68627
TC0100006623.hg.1 4.26852
TC0100006624.hg.1 5.2503
TC0100006627.hg.1 6.45613

Total number of rows: 13739

Table truncated, full table size 347 Kbytes.




Supplementary file Size Download File type/resource
GSM3580451_906_C-ex.CEL.gz 1.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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