Research Interests
Many vascular diseases are results of inappropriate reactivation of the same mechanisms that are essential for the development of blood vessels during embryogenesis. Accordingly, our main interest is to understand how the development of the vascular system is controlled in mouse embryos.
In general, blood vessel growth is triggered by hypoxic conditions in tissues. Lack of oxygen results in the accumulation of hypoxia inducible factor-1α and -2α (HIF-1α and -2α), both of which can upregulate the expression of the vascular endothelial growth factor-A (VEGF-A). VEGF-A regulates vascular development by interactions with a number of receptors, two of which are transmembrane tyrosine kinases Flt-1 (VEGFR-1) and Flk-1/KDR (VEGFR-2). We are investigating how VEGF-A receptors regulate vascular development in mouse embryos, with an extended interest in how these receptors coordinate with each other during both embryonic development and tumor angiogenesis.
Besides activating the expression of VEGF-A, HIF-1α and -2α may also have other functions in supporting the growth of blood vessels. Therefore, we are also studying how HIF-2α might control the development and maturation of the vascular system in mouse embryos by a mechanism that may be complementary to the induction of VEGF-A expression.
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