eurekalert.org
A novel discovery sheds light on the role of the adapter protein PICALM in white adipose tissue and its potential as a target for improving insulin sensitivity and glucose transport. This breakthrough, led by researchers from the German Institute of Human Nutrition Potsdam-Rehbruecke (DIfE), German Center for Diabetes Research (DZD), and collaborators, opens new avenues for treating type 2 diabetes (T2D) and obesity.
PICALM: More Than a Link to Alzheimer's Disease
PICALM has been widely studied for its connection to Alzheimer’s disease, but its role in metabolic health was previously unexplored. In this study, researchers discovered that reduced expression of PICALM in white adipose tissue enhances insulin sensitivity and glucose uptake in fat cells, pointing to a critical function in regulating glucose homeostasis. The findings, recently published in Molecular Metabolism, suggest that targeting PICALM could pave the way for innovative therapies to combat T2D and obesity.
What’s New?
This research marks the first time PICALM has been shown to regulate glucose transport in white adipose tissue. Using combined methods involving animal models, human subjects, and cell cultures, the research team found that lowering PICALM expression boosts the insulin-stimulated translocation of the GLUT4 glucose transporter to the cell surface, improving glucose uptake. Additionally, dietary interventions like intermittent fasting in mice and bariatric surgery in humans were shown to influence PICALM expression, offering potential non-pharmacological strategies for managing metabolic disorders.
Why It Matters
Obesity-related dysfunction in white adipose tissue is a major driver of type 2 diabetes, and insulin resistance is a hallmark of the disease. PICALM's role in regulating GLUT4 trafficking and insulin signaling directly affects glucose homeostasis, a critical factor in maintaining metabolic health. By modulating PICALM expression, there is potential to restore healthy glucose uptake in adipose tissue, reducing fatty acid release into the bloodstream and preventing fat accumulation in organs like the liver and muscles. These findings not only advance our understanding of adipose tissue function but also identify PICALM as a promising target for developing new treatments for T2D and obesity.
In the long term, targeting PICALM with medication or lifestyle interventions could significantly improve outcomes for patients with metabolic disorders. Future research aims to explore PICALM's role in skeletal muscles and its broader implications for glucose regulation across different tissues.