OKLAHOMA CITY – A new study from the University of Oklahoma reveals how a little-understood protein, CD82, contributes to blood vessel leakage, a process that initiates inflammation but becomes dangerous when it occurs during severe inflammatory diseases such as sepsis, acute respiratory distress syndrome and COVID-19. The findings , published in Nature Cardiovascular Research, could open the door to new therapies aimed at protecting patients from multi-organ failure and death in severe and systemic inflammation.
Blood vessel (vascular) leakage happens when blood vessels lose their ability to act as tight barriers, allowing fluid and proteins to escape into surrounding tissues. This condition, when it becomes dysregulated, is a hallmark of severe inflammation and contributes to life-threatening complications.
"CD82 is a type of protein called a tetraspanin, and while tetraspanins are known to regulate the formation of new blood vessels and the progression of cancer, their role in inflammation is less clear. This study found that CD82 makes blood vessels more prone to leak during inflammation. In our animal models, when we eliminated CD82 from blood vessels, the vascular leakage was substantially reduced during inflammation," said the paper's senior author, Xin Zhang, Ph.D., a professor of biochemistry and physiology at the University of Oklahoma College of Medicine and a member of OU Health Stephenson Cancer Center.
Zhang and his team also discovered that a small, active portion of cholesterol on the surface of the blood vessel cells is important in this process. CD82 interacts with this "accessible cholesterol," setting off signals inside the cells that make the blood vessels leakier. However, they also found that lowering this pool of cholesterol with a statin can strengthen vessel walls and reduce leakage.
"This research points to new strategies, including possibly repurposing drugs like statins, to stabilize blood vessels when the body is overwhelmed by inflammation," Zhang said. "However, these findings are based on preclinical research and will require further studies before being applied in human patients."
Zhang and his team have been continually funded by the National Institutes of Health and recently received a new NIH grant to continue this work.
