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PLoS One ; 12(8): e0182813, 2017.
Article in English | MEDLINE | ID: mdl-28859090

ABSTRACT

Angiogenesis is a highly coordinated, extremely complex process orchestrated by multiple signaling molecules and blood flow conditions. While sprouting mode of angiogenesis is very well investigated, the molecular mechanisms underlying intussusception, the second mode of angiogenesis, remain largely unclear. In the current study two molecules involved in vascular growth and differentiation, namely endoglin (ENG/CD105) and chicken ovalbumin upstream promoter transcription factor II (COUP-TFII) were examined to unravel their specific roles in angiogenesis. Down- respectively up-regulation of both molecules tightly correlates with intussusceptive microvascular growth. Upon ENG inhibition in chicken embryo model, formation of irregular capillary meshwork accompanied by increased expression of COUP-TFII could be observed. This dynamic expression pattern of ENG and COUP-TFII during vascular development and remodeling correlated with formation of pillars and progression of intussusceptive angiogenesis. Similar findings could be observed in mammalian model of acute rat Thy1.1 glomerulonephritis, which was induced by intravenous injection of anti-Thy1 antibody and has shown upregulation of COUP-TFII in initial phase of intussusception, while ENG expression was not disturbed compared to the controls but decreased over the time of pillar formation. In this study, we have shown that ENG inhibition and at the same time up-regulation of COUP-TFII expression promotes intussusceptive angiogenesis.


Subject(s)
COUP Transcription Factor II/genetics , Endoglin/genetics , Intussusception/genetics , Neovascularization, Pathologic/genetics , Animals , Blood Vessels/growth & development , Blood Vessels/metabolism , Cell Differentiation/genetics , Chick Embryo , Endoglin/antagonists & inhibitors , Gene Expression Regulation, Developmental , Glomerulonephritis/genetics , Glomerulonephritis/metabolism , Glomerulonephritis/pathology , Humans , Intussusception/pathology , Neovascularization, Pathologic/pathology , Protein Binding , Rats , Receptors, Notch/genetics , Signal Transduction/genetics , Smad Proteins/genetics
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