New stem cell lines developed from the skin of adults living with bipolar disorder are providing researchers at the U-M Health System an unprecedented opportunity to delve into the genetic and biological underpinnings of the devastating mood disorder. Scientists will be able to link new findings — such as how gene expression is affected by different medications — to extensive clinical and demographic data from the cell donors, who also are participants in an ongoing long-term study of hundreds of individuals with bipolar disorder.
The new research comes as the Heinz C. Prechter Bipolar Research Fund, based at the U-M Depression Center, prepares to mark the 10th anniversary of its establishment by Waltraud “Wally” Prechter following the July 2001 death of her husband, Heinz. Before he took his life, few people knew that the well-known automotive entrepreneur wrestled with bipolar disorder.
“Currently the best treatments for bipolar disorder are only effective for 30 percent to 50 percent of patients,” says Dr. Melvin McInnis, the Thomas B. and Nancy Upjohn Woodworth Professor of Bipolar Disorder and Depression at the Medical School and associate director the Depression Center. “New discoveries have been limited, in part due to the lack of access to tissue and cells from individuals with bipolar disorder. But that is now changing because of the Prechter research program and advances in stem cell research.”
The new stem cell lines — among the first to be created by the A. Alfred Taubman Medical Research Institute Consortium for Stem Cell Therapies — were made from fibroblasts from skin samples donated by adult research volunteers both with and without bipolar disorder.
In the lab, scientists can coax these skin cells into behaving like embryonic stem cells. Known as induced pluripotent stem cells, or iPSC, these, in turn, can be manipulated to develop into different types of body cells, including brain cells.
“We will be able to see if there are differences in how the neurons of a person with bipolar disorder make connections, determine how they respond to different medications and explore potential deficiencies in signaling pathways,” says Sue O’Shea, a professor of cell and developmental biology at the Medical School who leads the stem cell lab with Gary Smith, professor of obstetrics and gynecology.
So far, five lines have been created. The goal, O’Shea says, is to develop 30 cell lines — 20 from people with bipolar disorder and 10 control subjects. Creating each line is a painstaking and expensive process.
“We often think of stem cells being used in therapies to treat disease, but this is a great example of stem cells’ usefulness for studying the mechanisms of disease,” O’Shea says. “The iPS cells renew themselves, so they’re an unlimited source of material and offer hope to individuals with bipolar disorder.”
Still, the researchers caution, new treatments spurred by this work could be a decade or more away.
Bipolar disorder, formerly known as manic depression, affects 5.7 million adults in the United States. It is caused by chemical imbalances in the brain and marked by significant changes in mood, thoughts, energy and behavior. Because bipolar disorder runs in families, research at U-M has focused on studying disease genes. There is no single gene that “causes” someone to become bipolar, but the disease has its roots in genetic vulnerabilities.
The Prechter longitudinal study has already collected more than five years’ worth of data.
“I’m really proud that over the last 10 years my husband’s legacy has grown to include the strides we’re making to understand bipolar disorder and find new treatments,” Wally Prechter says. “Bipolar is like any other illness — cancer, diabetes, heart disease — and deserves the same urgency.”
