29. April 2024

Breakthrough in brown fat research Breakthrough in brown fat research

Researchers from Denmark and Germany have found brown fat’s “off-switch”

Researchers from the University of Southern Denmark, the Novo Nordisk Center for Adipocyte Signaling (SDU), the University of Bonn and the University Hospital Bonn (UKB) have found a protein that is responsible for turning off brown fat activity. This new discovery could lead to a promising strategy for safely activating brown fat and tackling obesity and related health problems. The results of the study have now been published in the journal „Nature Metabolism“.

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Brown fat, also known as brown adipose tissue (BAT), is a type of fat in our bodies that's different from the white fat around our belly and thighs that we are more familiar with. Brown fat has a special job—it helps to burn calories from the foods that we eat into heat, which can be helpful, especially when we're exposed to cold temperatures like during winter swimming or cryotherapy. For a long time, scientists thought that only small animals like mice and newborns had brown fat. But new research shows that a certain number of adults maintain their brown fat throughout life. Because brown fat is so good at burning calories, scientists are trying to find ways to activate it safely using drugs that boost its heat-producing abilities.

A new study from the research groups of Prof. Jan-Wilhelm Kornfeld from the University of Southern Denmark and the Novo Nordisk Center for Adipocyte Signaling and Dagmar Wachten from the University Hospital Bonn and the University of Bonn (Germany) has found that brown fat has a previously unknown built-in mechanism that switches it off shortly after being activated. This limits its effectiveness as treatment against obesity. According to first author of the study, Hande Topel, who is a Senior Postdoc at the University of Southern Denmark and the Novo Nordisk Center for Adipocyte Signaling (Adiposign), the team has now discovered a protein responsible for this switching-off process. It is called ‘AC3-AT’.

Blocking the "off switch" opens up a new strategy

“Looking ahead, we think that finding ways to block AC3-AT could be a promising strategy for safely activating brown fat and tackling obesity and related health problems”, Hande Topel says. The research team found the switch-off protein using advanced technology predicting unknown proteins. Hande Topel explains: “When we investigated mice that genetically didn't have AC3-AT, we found that ...

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The authors  thank the Microscopy Core Facility of the Medical Faculty at the University of Bonn for providing help, services, and devices

Sajjad Khani, Hande Topel, Ronja Kardinal et al; Cold-induced expression of a truncated Adenylyl Cyclase 3 acts as rheostat to brown fat function; Nature Metabolism;
DOI: 10.1038/s42255-024-01033-8
https://www.nature.com/articles/s42255-024-01033-8

Prof. Dagmar Wachten
Institute for Innate Immunity at the University Hospital Bonn (UKB)
Cluster of Excellence ImmunoSensation2, TRA "Modeling" & "Life & Health", University of Bonn
Phone: (+49) 228/ 287-51978
E-Mail: Dagmar.Wachten@ukbonn.de

Prof. Jan-Wilhelm Kornfeld
Center for Adipocyte Signaling (ADIPOSIGN)
Department of Biochemistry and Molecular Biology, University of Southern Denmark.
Phone: +45 9350 7481
E-Mail: janwilhelmkornfeld@bmb.sdu.dk

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