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Series GSE37676 Query DataSets for GSE37676
Status Public on May 02, 2012
Title Expression data from control and Ascorbic Acid (AA) stimulated Mc-3T3-E1 osteoblasts
Organism Mus musculus
Experiment type Expression profiling by array
Summary Despite advances in investigating functional aspects of osteoblast (OB) differentiation, especially studies on how bone proteins are deposited and mineralized, there has been little research on the intracellular trafficking of bone proteins during OB differentiation. Collagen synthesis and secretion is markedly upregulated upon Ascorbic Acid (AA) stimulation. Understanding the mechanism by which collagen is mobilized in specialized OB cells is important for both basic cell biology and diseases involving defects in bone secretion and deposition. RabGTPases are major regulators on protein trafficking throughout the cell. In this study, we identified the Rab GTPases that are upregulated during 5-day AA differentiation of OBs using microarray analysis, namely Rab1, Rab3d and Rab27b.
We used microarrays to detail the global programme of gene expression underlying procollagen production and trafficking and identified up-regulated genes during this process.
 
Overall design Control Mc3T3-E1 cells and 5 day Ascorbic Acid stimulated cells were processed for RNA extraction and hybridization on Affymetrix microarrays.
 
Contributor(s) Nabavi N, Harrison RE
Citation(s) 23050002, 23740245
Submission date Apr 30, 2012
Last update date Sep 17, 2020
Contact name Noushin Nabavi
E-mail(s) [email protected]
Organization name University of Toronto
Street address 1265 Military Trail
City Toronto
ZIP/Postal code M1C 1A4
Country Canada
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (6)
GSM925429 Mc3T3 control_ 5day_rep1
GSM925430 Mc3T3 control_ 5day_rep2
GSM925431 Mc3T3 control_ 5day_rep3
Relations
BioProject PRJNA162555

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Supplementary file Size Download File type/resource
GSE37676_RAW.tar 22.4 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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