Adipose proteome analysis: Focus on mediators of insulin resistance

Xiaoli Chen, Sonja Hess

Research output: Contribution to journalReview articlepeer-review

24 Scopus citations


As is well known, adipose tissue is an important site for lipid metabolism and insulin-responsive glucose uptake. The recent discovery of the endocrine function of adipose tissue and the association of obesity with chronic low-grade inflammation in adipose tissue has reinforced the concept of the central role of adipose tissue in mediating obesity-linked insulin resistance and metabolic dysregulation. The study of adipose cells has provided new insights into the mechanism underlying insulin resistance as well as the therapeutic strategies for diabetes. Numerous efforts have been made in identifying key molecular regulators of insulin action and metabolism, including the utilization of advanced proteomics technology. Various proteomic approaches have been applied to identify the adipose secretome, protein-expression profiling and post-translational modifications in adipose cells in the pathological state. In this review, we summarize the recent advances in the proteomics of adipose tissue, and discuss the identified proteins that potentially play important roles in insulin resistance and diabetes.

Original languageEnglish (US)
Pages (from-to)827-839
Number of pages13
JournalExpert Review of Proteomics
Issue number6
StatePublished - Dec 2008

Bibliographical note

Funding Information:
Sonja Hess has received NIH grant number Z01 DK070004-04. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.


  • Adipocyte
  • Adipokine
  • Diabetes
  • Insulin resistance
  • Insulin signaling pathway
  • Phosphoproteome
  • Phosphorylation
  • Proteomics
  • Secretome


Dive into the research topics of 'Adipose proteome analysis: Focus on mediators of insulin resistance'. Together they form a unique fingerprint.

Cite this