Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/132191
Title: GENETIC AND FUNCTIONAL CHARACTERIZATION OF HEREDITARY INTRAOSSEOUS VASCULAR MALFORMATION
Authors: XIONG JINGWEI
Keywords: Vascular malformation, intraosseous, angiogenesis, ELMO2, DOCK1, RAC1
Issue Date: 18-Aug-2016
Citation: XIONG JINGWEI (2016-08-18). GENETIC AND FUNCTIONAL CHARACTERIZATION OF HEREDITARY INTRAOSSEOUS VASCULAR MALFORMATION. ScholarBank@NUS Repository.
Abstract: Vascular malformations are non-neoplastic expansions of blood vessels that arise due to errors in angiogenesis. Here we report loss-of-function mutations in ELMO2, which translates extracellular signals into cellular movements, as causative for autosomal recessive intraosseous vascular malformation (VMOS) in five different families. Individuals with VMOS suffer from life-threatening progressive expansion of the jaw, craniofacial and other intramembranous bones caused by malformed blood vessels that lack a mature vascular smooth muscle layer. Analysis of primary fibroblasts from an affected individual showed that absence of ELMO2 correlated with a significant down regulation of binding partner DOCK1, resulting in deficient RAC1-dependent cell migration. Unexpectedly, elmo2-knockout zebrafish appeared phenotypically normal, suggesting human-specific ELMO2 requirements in bone vasculature homeostasis or genetic compensation by related genes. The present findings highlight the necessity of ELMO2 for maintaining vascular integrity, specifically in intramembranous bones.
URI: http://scholarbank.nus.edu.sg/handle/10635/132191
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