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Home › Dataset Library › Integrative transcriptomic and proteomic analysis of osteocytic cells exposed to fluid flow reveals novel mechano-sensitive signaling...

Dataset: Integrative transcriptomic and proteomic analysis of osteocytic cells exposed to fluid flow reveals novel mechano-sensitive signaling pathways

Osteocytes, positioned within bone’s interstitial space, are subject to fluid flow upon whole bone loading. Such fluid flow is widely...

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Osteocytes, positioned within bone’s interstitial space, are subject to fluid flow upon whole bone loading. Such fluid flow is widely theorized to be a mechanical signal transduced by osteocytes, initiating a poorly understood cascade of signaling events mediating bone metabolism. The objective of this study was to utilize high-throughput approaches to examine the time course of flow-induced changes in osteocyte gene transcript and protein levels. Microarray analysis demonstrated fluid flow regulation of genes consistent with known anabolic loading responses, including Ptgs2, NF-κB inhibitors, MAP3 kinases, and Wnt/β-catenin pathway signaling molecules. However, two of the most highly up-regulated gene products—Cxcl1 and Cxcl2, confirmed by qPCR—have not previously been reported to be responsive to fluid flow. Gene ontology analysis suggested a highly significant inflammatory and immune response, with cellular functions including trafficking, cell-to-cell signaling, and tissue development. Proteomic analysis of the same samples demonstrated greatest up-regulation of the ATP-producing enzyme NDK, calcium-binding Calcyclin, and G protein-coupled receptor kinase 6. An integrative pathway analysis merging fold changes in transcript and protein levels predicted signaling nodes not directly detected at the sampled time points, including STAT3 and c-Myc. These results extend our knowledge of the osteocytic response to fluid flow, most notably up-regulation of Cxcl1 and Cxcl2 as a possible paracrine agent for osteoblastic and osteoclastic recruitment. Osteocyte-like MLO-Y4 cells were subjected to 2 hours of 10 dyn/cm2 oscillating fluid flow in parallel-plate fluid flow chambers and harvested for analysis at 0, 2, 8, and 24 hours post-flow incubation. Parallel control samples from sham treated cells were also collected at each time point.

Species:
mouse

Samples:
24

Source:
E-GEOD-42874

Updated:
Dec.12, 2014

Registered:
Nov.24, 2014


Factors: (via ArrayExpress)
Sample TREATMENT TIME
GSM1052653 sham 0hr
GSM1052653 sham 0hr
GSM1052653 sham 0hr
GSM1052656 flow 0hr
GSM1052656 flow 0hr
GSM1052656 flow 0hr
GSM1052659 sham 2hr
GSM1052659 sham 2hr
GSM1052659 sham 2hr
GSM1052662 flow 2hr
GSM1052662 flow 2hr
GSM1052662 flow 2hr
GSM1052665 sham 8hr
GSM1052665 sham 8hr
GSM1052665 sham 8hr
GSM1052668 flow 8hr
GSM1052668 flow 8hr
GSM1052668 flow 8hr
GSM105267 sham 24hr
GSM105267 sham 24hr
GSM105267 sham 24hr
GSM1052674 flow 24hr
GSM1052674 flow 24hr
GSM1052674 flow 24hr

Tags

  • bone
  • cell
  • interstitial space
  • osteocyte
  • point
  • protein

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