Journal of Molecular Medicine

, Volume 90, Issue 4, pp 435–445

Intermittent hypoxia activates temporally coordinated transcriptional programs in visceral adipose tissue

  • Sina A. Gharib
  • Abdelnaby Khalyfa
  • Amal Abdelkarim
  • Vijay Ramesh
  • Mohamed Buazza
  • Navita Kaushal
  • Bharat Bhushan
  • David Gozal
Original Article

DOI: 10.1007/s00109-011-0830-7

Cite this article as:
Gharib, S.A., Khalyfa, A., Abdelkarim, A. et al. J Mol Med (2012) 90: 435. doi:10.1007/s00109-011-0830-7

Abstract

Obstructive sleep apnea (OSA) is a prevalent disorder characterized by intermittent hypoxia (IH) during sleep. OSA is strongly associated with obesity and dysregulation of metabolism—yet the molecular pathways linking the effects of IH on adipocyte biology remain unknown. We hypothesized that exposure to IH would activate distinct, time-dependent transcriptional programs in visceral adipose tissue of mice. We exposed 36 mice to IH or normoxia for up to 13 days. We transcriptionally profiled visceral fat tissue harvested from the animals and performed functional enrichment and network analysis on differentially expressed genes. We identified over 3,000 genes with significant expression patterns during the time course of IH exposure. The most enriched pathways mapped to metabolic processes, mitochondrion, and oxidative stress responses. We confirmed the pathophysiological relevance of these findings by demonstrating that mice exposed to chronic IH developed dyslipidemia and underwent significant lipid and protein oxidation within their visceral adipose depots. We applied gene–gene interaction network analysis to identify critical controllers of IH-induced transcriptional programs in adipocytes—these network hubs represent putative targets to modulate the effects of chronic IH on adipose tissue. Our approach to integrate computational methods with gene expression profiling of visceral fat tissue during IH exposure shows promise in helping unravel the mechanistic links between OSA and adipocyte biology.

Keywords

Sleep apneaAdipocyteMicroarrayNetwork analysisMetabolismOxidative stress

Supplementary material

109_2011_830_MOESM1_ESM.pdf (750 kb)
Supplementary Fig. 1(PDF 750 kb)
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Supplementary Fig. 2(PDF 776 kb)
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Supplementary Table 1(PDF 598 kb)
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Supplementary Table 2(PDF 57 kb)
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Supplementary Table 3(PDF 34 kb)
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Supplementary Table 4(PDF 56 kb)
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Supplementary Table 5(PDF 32 kb)

Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Sina A. Gharib
    • 1
    • 2
  • Abdelnaby Khalyfa
    • 3
  • Amal Abdelkarim
    • 3
  • Vijay Ramesh
    • 3
  • Mohamed Buazza
    • 4
  • Navita Kaushal
    • 3
  • Bharat Bhushan
    • 3
  • David Gozal
    • 3
  1. 1.Center for Lung Biology, Department of MedicineUniversity of WashingtonSeattleUSA
  2. 2.Division of Pulmonary and Critical Care Medicine, Department of MedicineUniversity of WashingtonSeattleUSA
  3. 3.Department of PediatricsUniversity of ChicagoChicagoUSA
  4. 4.University of LouisvilleLouisvilleUSA