Hypoxia Downregulates the Angiogenesis in Human Placenta via Notch1Signaling Pathway
10.1007/s11596-017-1770-4
- Author:
LI YU-QI
1
;
LIU HAI-YI
;
CAO LAN-LAN
;
WU YUAN-YUAN
;
SHI XIN-WEI
;
QIAO FU-YUAN
;
FENG LING
;
DENG DONG-RUI
;
GONG XUN
Author Information
1. Department of Obstetrics and Gynecology
- Keywords:
hypoxia;
Notch 1;
Dell4;
Jaggedl;
angiogenesis;
human umbilical vein endothelial cells;
placenta
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2017;37(4):541-546
- CountryChina
- Language:Chinese
-
Abstract:
Placentation,which is critical for maternal-fetal exchange of nutrients and gases,is a complicated process comprising stepwise vasculogenesis and angiogenesis.Hypoxia caused by impairedtrophoblast invasion may cause various angiogenic abnormalities in human placenta.The Notchl signaling pathway plays an important role in the regulation of angiogenesis.The angiogenesis of human umbilical vein endothelial cells (HUVECs) under normal/hypoxic conditions and the mRNA/protein level of Notchl/Dell4/Jaggedl were investigated in this study.The effects of DAPT/JAG-1 on the migration of HUVECs were also assessed by cell wound healing assay,so as to discover the possible role of notchl signaling pathway in the angiogenesis of human placenta.The results showed that angiogenic ability of HUVECs was seriously reduced under hypoxic conditions.The mRNA and protein levels of Notchl/Dell4/Jaggedl were decreased in the hypoxic group compared to the control one.In addition,the migration capability of HUVECs was significantly obstructed when treated with DAPT and under hopoxic condition,but promoted when treated with JAG-1.The above results demonstrate that hypoxia downregulates the angiogenesis in human placenta via Notch 1 signaling pathway.
