“We have shown in animal studies that removing the ALK7 receptor improves insulin release by beta-cells in the pancreas, and at the same time decreases fat deposition in situations of high caloric intake”, says Professor Carlos Ibáñez, who lead the two studies that are now published as back-to-back papers in the PNAS. “The well-known connections between diabetes and obesity make our combined findings quite exciting.”

Up to 6 per cent of the world population is estimated to suffer from some form of diabetes, either due to a reduced ability to produce insulin, or to insulin resistance. Insulin is a hormone required by cells in the body to absorb glucose from the blood, thereby providing them with energy. Obesity has been shown to increase the risk of developing diabetes, and as overweight becomes more prevalent in the human population, so do the cases of diabetes.

The research group led by Carlos Ibáñez studies how signaling by growth factors and their receptors regulate different physiological functions in the body. They have recently investigated the functions of one of these receptors, called ALK7, using mutant mice (knock-out mice) lacking this receptor. They found that in the absence of ALK7, mice developed abnormally high levels of insulin in the blood, which with age led to insulin resistance and liver steatosis, a pathological condition in which the liver enlarges and accumulates abnormally high levels of fat.

In collaboration with another research group at Karolinska Institutet, led by Professor Per-Olof Berggren, they also found that Calcium signaling in pancreatic beta-cells was reduced by the actions of the growth factor Activin B through the ALK7 receptor, and that blood glucose levels regulates the expression of both Activin B and ALK7. In agreement with these results, mice lacking Activin B also developed hyperinsulinemia to a similar extent as ALK7 mutants.

“In other words, our data revealed an unexpected negative feedback loop in the control of glucose-dependent insulin release, mediated the actions of Activin B on the ALK7 receptor”, says Carlos Ibáñez.

In the second study, the scientists found that mice lacking ALK7 accumulated less fat and gained less weight than their normal counterparts when fed on a high-fat diet. They discovered that another growth factor called GDF3 could also signal via the ALK7 receptor, and that mice lacking GDF3 showed similar defects in fat deposition and weight gain as the ALK7 mutants. Intriguingly, however, mutant mice consumed equal amounts of food as their normal counterparts during the experiment.

“These results show that lack of ALK7 or GDF3 improves energy balance in the body under regimes of high caloric intake”, says Carlos Ibáñez.

Publications:

‘Activin B receptor ALK7 is a negative regulator of pancreatic ß-cell function’, Philippe Bertolino, Rebecka Nilsson, Eva Reissmann, Olov Andersson, Per-Olof Berggren and Carlos F. Ibáñez, PNAS, online early edition, 12-16 May 2008.

‘Growth/Differentiation Factor 3 signals through ALK7 and regulates accumulation of adipose tissue and diet-induced obesity’, Olov Andersson, Marion Korach-Andre, Eva Reissmann, Carlos F. Ibáñez och Philippe Bertolino, PNAS, online early edition, 12-16 May 2008.

For further information, please contact:

Professor Carlos Ibáñez
Phone +46 (0)8-524 87660
Email: carlos.ibanez@ki.se

Press Officer Katarina Sternudd
Phone: +46 (0)8-524 838 95
Mobile: +46 (0)70-224 38 95
Email: katarina.sternudd@ki.se

Karolinska Institutet is one of the leading medical universities in Europe. Through research, education and information, Karolinska Institutet contributes to improving human health. Each year, the Nobel Assembly at Karolinska Institutet awards the Nobel Prize in Physiology or Medicine. For more information, visit ki.se