News

Mouse study provides new clue to staying skinny on a high-fat diet


1 May 2013

Dr Kim Bell-Anderson: "To our surprise we found that mice without the protein KLF3 remained lean on a high-fat diet."
Dr Kim Bell-Anderson: "To our surprise we found that mice without the protein KLF3 remained lean on a high-fat diet."

The mystery of why some people get fat eating high-fat foods while others can stay skinny on a diet of burgers and chips is closer to being solved.

Research led by the University of Sydney in collaboration with the University of NSW investigated a genetically modified strain of mice. The researchers unexpectedly found that the mice remained thin on a high-fat diet.

The findings are published today in the journal Diabetes.

The researchers already knew that a protein called KLF3 turns off genes involved in blood production.

"We were trying to work out the function of the protein KLF3 by making a mouse that didn't have any KLF3. To our surprise we found that these mice remained lean on a high-fat diet. They also showed signs of improved glucose metabolism and insulin action," said Dr Kim Bell-Anderson, from the University of Sydney's School of Molecular Bioscience, and the lead author of the study.

"We knew KLF3 was important for turning off gene expression, but we didn't know which genes it targeted, so we looked at the gene expression of about 20,000 genes to see which ones were abnormally expressed in our mutant mice."

Researchers from Professor Merlin Crossley's laboratory in the University of NSW's School of Biotechnology and Biomolecular Sciences used the Ramaciotti Centre facility to carry out the genome analysis.

"One of our investigators, Dr Alister Funnell, noticed that the expression of a gene, recently discovered to encode a hormone called adipolin, was increased in the mutant mice," said Professor Crossley.

Adipolin is a type of hormone, produced by fat cells, that enters the blood and modulates responses to food.

If mice have a lot of adipolin they can better maintain a stable blood glucose level and remain thin even on a high fat diet. If mice have less adipolin they can't lower their blood glucose levels after a meal and are fatter.

"The amount of adipolin circulating in the blood of our mutant mice was more than doubled," said Dr Bell-Anderson.

"The roles of KLF3 and adipolin in humans and their beneficial or harmful effects are yet to be determined, but therapies aimed at increasing adipolin levels may be a promising target for treatment of type 2 diabetes and obesity."


Follow University of Sydney Media on Twitter

Media enquiries: Verity Leatherdale, 02 9351 4312, 0403 067 342, verity.leatherdale@sydney.edu.au