Intestinal microcirculation and necrotizing enterocolitis: The vascular endothelial growth factor system

被引:66
作者
Bowker, Rakhee M. [1 ]
Yan, Xiaocai [2 ]
De Plaen, Isabelle G. [2 ,3 ]
机构
[1] Rush Univ, Med Ctr, Dept Pediat, Sect Neonatol, Chicago, IL 60612 USA
[2] Northwestern Univ, Dept Pediat, Ann & Robert H Lurie Childrens Hosp Chicago, Div Neonatol,Feinberg Sch Med, Chicago, IL 60611 USA
[3] Northwestern Univ, Ann & Robert H Lurie Childrens Hosp Chicago, Stanley Manne Childrens Res Inst, Ctr Intestinal & Liver Inflammat Res, Chicago, IL 60611 USA
关键词
Angiogenesis; Intestinal ischemia; Intestinal microvasculature; Intrauterine infection; intrauterine inflammation; Necrotizing enterocolitis; Vascular endothelial growth factor; Vascular endothelial growth factor receptor 2; VEGF; FETAL; MICROVASCULATURE; PATHOPHYSIOLOGY; RETINOPATHY; MICROBIOTA; DOPPLER;
D O I
10.1016/j.siny.2018.08.008
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Necrotizing enterocolitis (NEC), a leading cause of morbidity and mortality in preterm neonates, is a devastating disease characterized by intestinal tissue inflammation and necrosis. NEC pathogenesis is multifactorial but remains unclear. Translocation of bacteria and/or bacterial products across a weak intestinal barrier in the setting of impaired mucosal immunity leads to an exaggerated inflammatory response and secondary mucosal epithelial injury. In addition to prematurity, other risk factors for NEC include congenital heart disease, maternal pre-eclampsia with placental vascular insufficiency, severe anemia and blood transfusion all conditions that predispose the intestine to ischemia. We recently found that maldevelopment of the intestinal microvasculature plays an important role in NEC pathogenesis. Here we review the evidence supporting a role for defective development of the intestinal mucosal microvasculature and perturbations of intestinal blood flow in NEC, emphasizing the importance of vascular endothelial growth factor (VEGF) and the VEGF receptor-2 signaling pathway.
引用
收藏
页码:411 / 415
页数:5
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