Their study appears in the April 29 issue of Developmental Cell.
Arteries form in utero and during development, but can also form in adults when organs become deprived of oxygen — for example, after a heart attack. The organs release a molecular signal called VEGF. Working with mice, the Yale-UCL team discovered that in order for VEGF-driven artery formation to occur, VEGF must bind with two molecules known as VEGFR2 and NRP1, and all three must work as a team.
The researchers examined mice that were lacking a particular part of the NRP1 molecule that transports VEGF and VEGFR2 to a signaling center inside blood vessel walls. They observed that the internal organs of these mice contained poorly constructed arterial branches. Further, the mice where unable to efficiently repair blood vessel blockage through the formation of new arteries.
“We have identified an important new mechanism that regulates VEGFR2 transport in vascular cells,” said corresponding author Michael Simons, professor of medicine and cell biology, and director of the cardiovascular research center at Yale School of Medicine. “This opens new therapeutic opportunities for developing drugs that would either stimulate or inhibit blood vessel formation — important goals in cardiovascular and anti-cancer therapies, respectively.” Simons also has an appointment as honorary professor of medicine at UCL.
The Yale-UCL collaboration began more than three years ago, as an intensive global effort to improve the human condition through biomedical research and translational medicine. The Yale-UCL alliance has provided many opportunities to date for high-level scientific research, and clinical and educational collaboration.
Co-senior author is Christiana Ruhrberg, professor of neuronal and vascular development at the Institute of Ophthalmology at University College London. Ruhrberg also has an appointment as adjunct professor of medicine at Yale School of Medicine.
Other authors are A. Lanahan, X. Zhang, Z.W. Zhuang, F. Rivera-Molina, C. Prahst, J. Zhang, Y. Wang, D. Toomre of Yale; A. Fantin of University College London, and K.R. Speichinger and G.E. Davis of the University of Missouri.
The study was supported by grants from the National Institutes of Health (HL62289) and a Wellcome Trust Junior Investigator award.
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