Researchers discover new mechanism which may stimulate blood vessels' inner liner

Blood vessels are the body's transportation system, carrying oxygen and nutrients to cells and whisking away waste. But this vital mission can also be co-opted by tumors or break down as a result of disease, and this process has been poorly understood. An international collaborative team led by a scientist at Tokyo University of Agriculture and Technology (TUAT) in Japan has discovered a mechanism by which the growth of these vessels' inner liner is stimulated, which may lead to therapeutics that could cut vessels off from tumors or help rebuild vessels in degenerative diseases.

The results were published on April 2 in Communications Biology, a Nature journal.

The researchers studied how the endothelial cells lining the inside of blood vessels respond to hydrostatic pressure, which is the pressure that forces blood through the vessels. The single layer of these cells forms a barrier between vessels and tissue, which controls fluid's flow in the blood vessel walls.

Blood vessels are constantly exposed to stimuli such as fluid shear stress, cyclic tensile force and hydrostatic pressure. Although the detailed mechanisms about cellular responses to shear stress and tensile force have been studied, we have not well understood how hydrostatic pressure affects vascular function."

Daisuke Yoshino, paper author and associate professor at the TUAT

Yoshino and his team applied the pressure to endothelial cells, equivalent of a person working out, to investigate how they sense hydrostatic pressure and convert it into biochemical signals, inducing vascular responses. They found that the increase in pressure triggered a water transfer through a channel called aquaporin 1, which activated a protein signaling channel called Ras-ERK. This process induced endothelial cell growth, indicating a clear connection between pressure stimulation and intracellular biochemical signals, according to Yoshino.

"Our ultimate goal is to comprehensively clarify how the mechanisms described in this study are altered by differences in the blood pressure conditions, such as local conditions, magnitude and mode by which it is exerted," Yoshino said. "We hope the clarified mechanisms will lead to the development of new treatments for diseases invoking abnormalities in vascular formation, such as venous malformations."