News Release

New cellular player involved in obesity discover

Researchers have discovered that blocking a protein called 'iRhom2' in mice increases energy consumption in fat depots called adipose tissue

Peer-Reviewed Publication

Instituto Gulbenkian de Ciencia

Marina Badenes, Instituto Gulbenkian de Ciencia

image: Researcher and paper author. view more 

Credit: Ana Morais

The prevalence of obesity, a disease considered a serious public health problem, is increasing globally. In Portugal, almost half of the population is overweight and close to one million adults suffer from obesity. Known as a risk factor for the development of cardiovascular disease and diabetes, obesity is associated with chronic inflammation in fat tissues. New strategies to fight this disease are needed. Therefore, a deeper understanding of the mechanisms involved in metabolic deregulation are critical to approach the obesity problem.

To Colin Adrain, principal investigator of the research group, "it is important to understand the fundamental mechanisms underlying how metabolic dysregulation occurs." Adrain added that during the research they found that "iRhom2 protein is strongly present in metabolic tissues and organs, which made us decide to study the role of iRhom2 in obesity in more detail."

The paper, now published in the Molecular Metabolism journal, demonstrates how the researchers reached these results: they used an animal model, comparing groups with iRhom2 deletion to controls, and feeding them with normal diet versus a high fat diet.

Surprisingly, they found that during obesity, iRhom2 protein levels increase specifically in brown adipose tissue in obese animals compared to controls. Following up on this, they found that, on a high fat diet, the animals lacking iRhom2 protein were metabolically more healthy than their wild type counterparts.

Marina Badenes, a researcher and the main author of the paper, explains that "the deletion of iRhom2 led to enhanced energy consumption in adipose tissue, which protected animals from fat accumulation and inflammation, fatty liver and insulin resistance when the animals were placed on a diet that predisposed them to obesity". Furthermore, the researchers found that "at the cellular level deletion of iRhom2 leads to an increase in thermogenesis (heat production) in brown adipose tissue. Thermogenesis in brown adipose tissue is an important physiological mechanism to consume excess body energy".

Interestingly no deleterious side effects were found in the animals with iRhom2 deletion, indicating that blocking iRhom2 may potentially be beneficial in the treatment of obesity and associated complications. Researchers intend to continue the project to further understand the mechanisms and cell types involved in the iRhom2 control of obesity. They also want to find out the specific targets involved in the protection against obesity associated with loss of iRhom2.


This research project involved several Labs of the IGC (Membrane Traffic, Obesity, and Innate Immunity and Inflammation) and International Institutes: NeurObesity Group from the Center for Research in Molecular Medicine and Chronic Diseases (CiMUS) and CIBER (Spain), the Girona Biomedical Research Institute (Spain) and the Institute of Metabolic Science (UK).

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