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New findings on glucagon synthesis

Per-Olof Berggren Photo: Ulf Sirborn

While insulin is a hormone that lowers the level of glucose in the blood, glucagon is a hormone that increases it. Associate Professors Barbara and Ingo Leibiger and Professor Per-Olof Berggren at Karolinska Institutet have already published results showing that the insulin-producing cells are activated by the very hormone they release. Whether this process applies only to insulin or whether it reflects a general biological principle for all hormone-secreting cells has, however, remained unclear.

Now, the same team have shown that glucagon can also stimulate its own synthesis. This it does by binding to a specific binding site on the glucagon-secreting cells in the pancreas, where it subsequently influences a number of signalling pathways that lead to the activation of the gene that produces glucagon. It thus seems that the positive-feedback process, whereby secreted hormones affect their own production, has general biological significance.

“Learning about how the hormones regulate their own production will eventually enable us to study defects in this process, and if these defects are implicated in diabetes, then an important piece of the puzzle might well be in place,” says Per-Olof Berggren.

The study was financed by grants from the Swedish Research Council, the Novo Nordisk Foundation, the Swedish Diabetes Association, the Knut and Alice Wallenberg Foundation, the European Foundation for the Study of Diabetes (EFSD), the Diabetes Research and Wellness Foundation, the Berth von Kantzow Foundation, Skandia, the National Research Foundation of Korea, the Strategic Research Programme in Diabetes at Karolinska Institutet, the Stichting af Jochnick Foundation, and the Erling-Persson Family Foundation.


Barbara Leibiger, Tilo Moede, Thusitha P. Muhandiramlage, Daniel Kaiser, Pilar Vaca Sanchez, Ingo B. Leibiger, and Per-Olof Berggren

Glucagon regulates its own synthesis by autocrine signaling

Proceedings of the National Academy of Sciences (PNAS), Early Edition 3-7 December 2012

For further information, please contact:

Professor of experimental endocrinology Per-Olof Berggren

+46 (0)70-729 57 31

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