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Sample GSM1409756 Query DataSets for GSM1409756
Status Public on Jun 11, 2014
Title tr_5h_446
Sample type RNA
 
Source name cyclic mechanical stretched primary human dermal fibroblasts, 5h, subject 8
Organism Homo sapiens
Characteristics individual: subject 8
cell type: primary dermal fibroblasts
treatment: cyclic mechanical stretching
time: 5h
Treatment protocol Mechanical stretching was performed on flexible silicon membranes using FX-4000T™ Tension Plus™ System (Flexercell International Corporation, Hillsborough, USA). Cells were seeded on Bioflex culture plates and after 24 h subjected to stretching experiments or left untreated as control. Cyclic stretch was applied for 5 h and 24 h in the FX-4000T ™ Tension Plus™ System with 16% Elongation, 0.5 Hz in a half sinus regimen. Cell alignment was observed at the outer circular region of the well. Control cells were left static for 5 h and 24 h, as well.
Growth protocol Primary human dermal fibroblasts were isolated from skin biopsies obtained from plastic surgery by collagenase digestion and stored at -170°C in DMSO until usage. All donors provided written, informed consent. For experiments cells were cultured only until the third passage in Dulbecco’s modified Eagle’s Medium (DMEM, 4.5 g/l glucose) containing 10% fetal calf serum, 2 mM L-alanyl-L-glutamine and 0.1 mg/ml penicillin/streptomycin at 37°C in an atmosphere of 5% CO2 and 90% humidity.
Extracted molecule total RNA
Extraction protocol To separate the inhomogeneous stretching areas of the BioFlex culture plates the silicon membranes were punched with a 2 cm diameter punch. Isolation of RNA was done with Rneasy Mini kit according to manufacturer product information from the outer cicular region of the well. DNA and RNA were precipitated with 70 % ethanol and bound to a column. DNA was digested using DNAse I. RNA was eluted with 30 µl RNAse free water and subjected to Experion automated electrophoresis using the Experion RNA StdSens Analysis Kit (Bio-Rad, Hercules, USA) for quality control.
Label Cy3
Label protocol For the linear T7-based amplification step, 100ng of each total RNA sample was used. To produce Cy3-labeled cRNA, the RNA samples were amplified and labeled using the Agilent Low Input Quick Amp Labeling Kit (Agilent Technologies) following the manufacturer's protocol. Yields of cRNA and the dye-incorporation rate were measured with ND-1000 Spectrophotometer (NanoDrop Technologies)
 
Hybridization protocol The hybridization procedure was performed according to the Agilent 60-mer oligo microarray processing protocol using the Agilent Gene Expression Hybridization Kit (Agilent Technologies) (Design ID 028004). Briefly, 600 ng Cy3-labeled fragmented cRNA in hybridization buffer was hybridized 17 h at 65°C to Agilent whole genome oligo microarrays 8X60K using Agilent's recommended hybridization chamber and oven. Finally, the microarrays were washed once with the Agilent Gene Expression wash buffer 1 for 1 min at room temperature followed by a second wash with preheated Agilent Gene Expression wash buffer 2 (37 °C) for 1 min. The last washing step was performed with acetonitrile.
Scan protocol Fluorescence signals of the hybridized Agilent microarrays were detected using Agilent's Microarray Scanner System (G2505C, Agilent Technologies, Palo Alto, USA)..
Description Gene expression after 5h cyclic mechanical stretching
Reu_35
Data processing The Agilent Feature Extraction Software (FES 10.7.3.1 ) was used to read out and process the microarray image files. The preprocessing proper started with the conversion of the data after using Agilent Feature Extraction software in a format suitable for all subsequent analysis steps, which were mainly performed with the R statistical software and its Bioconductor packages. For the preprocessing the agi4x44kpreprocess package was used. To this end an annotation package for the Agilent Whole Genome 8x60K chip has (previously) been created. After reading the data files into R, all data were background-corrected. Data were then normalized between arrays using quantile-normalization and transformed to log2-scale, which enabled comparison of samples loaded on different arrays. After normalization, a set of quality control steps were performed to filter low-quality probes. Filtering of probes was based on quality flags set by the Agilent Feature Extraction Software. Most of the probes (~42 %) were filtered because of not being sufficiently above background. Finally, the processed data were stored in formats that allowed further downstream analyses and easy access.
 
Submission date Jun 11, 2014
Last update date Jun 11, 2014
Contact name Maria Reichenbach
Organization name Freie Universität Berlin
Department Institute for Chemistry and Biochemistry
Lab Signal transduction
Street address Thielallee 63
City Berlin
ZIP/Postal code 14195
Country Germany
 
Platform ID GPL13607
Series (1)
GSE58389 Cyclic mechanical stretch-induced gene expression

Data table header descriptions
ID_REF
VALUE normalized signal intensity

Data table
ID_REF VALUE
4 8.355887239
5 9.80314739
6 6.286429634
7 11.83191821
8 8.182554804
9 5.689520797
10 6.556742994
11 5.998819192
12 9.137805332
13 9.127555476
14 7.532067416
15 12.50321438
16 5.689520797
17 8.358957573
18 5.895268565
19 6.100452116
20 10.15777518
21 10.04358824
22 6.014839956
23 6.151749521

Total number of rows: 62973

Table truncated, full table size 1089 Kbytes.




Supplementary file Size Download File type/resource
GSM1409756_252800418237_S01_GE1_107_Sep09_1_3.txt.gz 12.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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