Transcription profiling of mouse chondrocytes treated with MEK/ERK pathway inhibitors
Ontology highlight
ABSTRACT: Objectives: To identify similarities and differences in gene expression data in the MEK/ERK and PI3K pathways and to determine how histone modification affects these same pathways. Goal: To identify and functionally characterize novel targets of these signaling pathways in the context of chondrocyte differentiation. Experiment Overall Design: Cartilage derived from the hind limbs of CD1 mice staged at 15.5 days of embryonic development were dissected and plated in primary chondrocyte monolayer cultures. Cells were treated with MEK/ERK pathway inhibitors (SB202190 and UO126), a PI3K inhibitor (LY294002), a histone deacetylase inhibitor (Trichostatin A) and the vehicle control (DMSO) for 24 hours. Total RNA was isolated from these samples and hybridized to Affymetrix MOE 430 2.0 chips at the
ORGANISM(S): Mus musculus
SUBMITTER: veronica ulici
PROVIDER: E-GEOD-15069 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
ACCESS DATA