Secret Ingredient to Growing Blood Vessels Found

“Most of the studies of angiogenesis [blood vessel formation] have focused on the inner lining of the pipes themselves,” researcher Daniel L. Hess said. “That’s fairly well understood. But it’s really not well understood how you get a complete functional blood vessel that can withstand the mechanical force exerted by blood pressure.”

UVA’s new discovery helps answer that – and, in so doing, saves scientists from the time, effort and cost of pursuing treatment strategies that will ultimately bear no fruit.

Innovation and Collaboration

The discovery was made possible by the fortuitous convergence of research in two different labs at UVA. Hess was working on a model of peripheral artery disease in the labs of Owens and UVA’s Brian Annex, MD, in the Robert M. Berne Cardiovascular Research Center, while another researcher, Molly R. Kelly-Goss, was working with a model of blood vessel growth she developed in the lab of Shayn M. Peirce, PhD, of UVA’s Department of Biomedical Engineering.

By bringing those two models together, the researchers were able to determine the vital role of the perivascular cells in blood vessel formation and to identify a gene, Oct4, that is required for this process. Previously, Oct4 had been thought to be active only in embryonic stem cells during early development and to be permanently inactivated in adult organisms. This belief persisted until two years ago, when the Owens lab showed it was reactivated within smooth muscle cells during formation of atherosclerotic plaques inside blood vessels and required for formation of a protective fibrous cap on those lesions that prevents them from rupturing and setting off a heart attack or stroke – analogous to a patch on a tire. Now the lab has shown that Oct4 has an important role in the formation of the vessels themselves – ironically, being required for forming the protective outer wall of blood vessels.

Using Kelly-Goss’ model, the researchers were able to examine blood vessel formation in real time. They found that vessels that lacked perivascular cell coverage formed incompletely and leaked blood. “Multiple failed trials assumed the perivascular cells were just passive followers,” Owens explained. But without them, he said, “the whole process comes to a halt.” Importantly, they found that endothelial cells and perivascular cells communicate with one another via Oct4-dependent processes and, without it, functional non-leaky blood vessels or blood vessel networks cannot form.

Ultimately, that means that scientists must take a more sophisticated approach to growing new vessels, a process important in normal growth and reproduction as well as wound repair.

The researchers have published their findings in the scientific journal Nature Communications. The research team consisted of Hess, Kelly-Goss, Olga A. Cherepanova, Anh T. Nguyen, Richard A. Baylis, Svyatoslav Tkachenko, Annex, Peirce and Owens.

Contacts and sources:
Josh Barney
University of Virginia School of Medicine