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>  News Releases >   2003 >   June

Missing link detected in insulin mechanism

Posted 06/27/03, by Hali Wickner


Professor of Biochemistry Gustav Lienhard
Findings could shed light on Type II diabetes and insulin resistance

Dartmouth Medical School biochemists have discovered a protein that appears to be a missing link in understanding how the hormone insulin regulates the movement of glucose into cells.

Professor of Biochemistry Gustav Lienhard presented the work on June 21 at the 85th Annual Meeting of The Endocrine Society in Philadelphia and in a recent issue of the Journal of Biological Chemistry. The findings by Lienhard and his fellow researchers at Dartmouth and Harvard could provide clues for understanding Type II diabetes, which is often characterized by insulin resistance. The findings could also shed light on how hormones regulate movement of membrane proteins in general, Lienhard said. "The protein is found in all the major tissues in the body - brain, liver, kidney - so it could function in other systems where a hormone treatment causes the rapid movement of proteins to the cell surface," Lienhard said.

Insulin acts to maintain the appropriate level of glucose in the blood. One way insulin does that is to accelerate the removal of glucose from blood and into muscle and fat cells. These muscle and fat cells have proteins known as "transporters" that can ferry glucose into the cells. However, the transporters are located deep within the cell in vesicles, and so are not immediately available for glucose movement. Insulin presses on the outside of the muscle or fat cell, prodding the vesicles within the cell to fuse with the surface membrane. This makes the transporters available to carry glucose into the cell more rapidly.

Lienhard likens the process to a room with too few doors. "You have a lot of people wanting to get into a room that only has two doors. But inside the room is a stack of doors. People are the glucose molecules and the doors are the transporters; in response to insulin, these doors get shoved into the walls of the room and more people can get into the room quickly.

"That was a missing link in this field. If we're right, this looks like a key protein that connects signaling to trafficking. At the end of the signal transduction pathway, we found a protein that's modified by phosphorylation - by putting phosphate groups on it - and this protein also acts on a key protein component in the machinery for vesicle movement and fusion," Lienhard said.

Insulin binding to its receptor on the outside of the cell membrane initiates a series of actions. That receptor extends through to the inner surface of the membrane and triggers signaling steps, or a signal transduction pathway, that eventually leads to the vesicle movement and fusion.

The protein seems to bridge the signaling and membrane movement, a span between the signal transduction pathway and the machinery that controls the fusion of the transporter-containing vesicles with the cell surface.

- Hali Wickner

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