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Protein identified that modulates metabolic dysfunction in obesity

Date:
June 21, 2010
Source:
Boston University Medical Center
Summary:
Researchers have discovered that Sfrp5, which refers to secreted frizzled-related protein 5, is an anti-inflammatory adipokine whose expression is disrupted in animal models of obesity and type 2 diabetes. The findings may provide a new way of targeting metabolic disease, specifically obesity.

Researchers from Boston University School of Medicine (BUSM) have discovered that Sfrp5, which refers to secreted frizzled-related protein 5, is an anti-inflammatory adipokine whose expression is disrupted in animal models of obesity and type 2 diabetes. The findings, which currently appear online in Science, may provide a new way of targeting metabolic disease, specifically obesity.

Obesity is a predisposing factor for metabolic disorders such as type 2 diabetes, which is often associated with a low-grade inflammatory state in adipose tissue. Adipose tissue secretes a variety of cytokines, referred to as adipokines. Most adipokines, such as tumor necrosis factor (TNF) α, interleukin (IL)-6 and leptin, are pro-inflammatory. One prominent exception is adiponectin, an anti-inflammatory adipokine that promotes insulin sensitization and protects cardiovascular tissue from ischemic injury.

According to the researchers, because adipokine dysregulation can contribute to the pathogenesis of obesity-linked disorders, they sought to identify new adipokines by comparing the gene expression profile of adipose tissue from lean mice with that from obese mice on a high calorie diet.

"Our study shows that Sfrp5 is secreted by adipocytes and that it controls the microenvironment of white adipose tissue under conditions of obesity-induced metabolic stress. Whereas Sfrp5 deficient mice do not express a detectable phenotype when fed a normal diet, these animals displayed aggravated fat pad inflammation and systemic metabolic dysfunction when fed a high calorie diet," explained senior author Kenneth Walsh, PhD, director of the Whitaker Cardiovascular Institute at BUSM. Conversely, the BUSM researchers found the administration of Sfrp5 to models of obese and diabetic mice improved metabolic function and reduced adipose tissue inflammation.

The researchers propose that Sfrp5 neutralizes noncanonical JNK activation by Wnt5a in macrophages and adipocytes via paracrine and autocrine mechanisms, respectively. "The JNK signaling pathway in adipocytes and macrophages has emerged as an important mediator of adipose tissue inflammation that affects systemic metabolism. Thus, the Sfrp5-JNK1 regulatory axis in fat represents a potential target for the control of obesity-linked abnormalities in glucose homeostasis," added Walsh.

Funding for this study was provided by the National Institutes of Health.


Story Source:

The above story is based on materials provided by Boston University Medical Center. Note: Materials may be edited for content and length.


Journal Reference:

  1. Noriyuki Ouchi, Akiko Higuchi, Koji Ohashi, Yuichi Oshima, Noyan Gokce, Rei Shibata, Yuichi Akasaki, Akihiko Shimono, and Kenneth Walsh. Sfrp5 Is an Anti-Inflammatory Adipokine That Modulates Metabolic Dysfunction in Obesity. Science, June 17, 2010 DOI: 10.1126/science.1188280

Cite This Page:

Boston University Medical Center. "Protein identified that modulates metabolic dysfunction in obesity." ScienceDaily. ScienceDaily, 21 June 2010. <www.sciencedaily.com/releases/2010/06/100617143940.htm>.
Boston University Medical Center. (2010, June 21). Protein identified that modulates metabolic dysfunction in obesity. ScienceDaily. Retrieved October 20, 2014 from www.sciencedaily.com/releases/2010/06/100617143940.htm
Boston University Medical Center. "Protein identified that modulates metabolic dysfunction in obesity." ScienceDaily. www.sciencedaily.com/releases/2010/06/100617143940.htm (accessed October 20, 2014).

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