Low-dose mifepristone increased angiogenesis in a manner involving AQP1
Low-dose mifepristone increased angiogenesis in a manner involving AQP1
复制标题
低剂量米非司酮通过涉及 AQP1 的方式增加血管生成
DOI:
10.1007/s00404-018-4989-9
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发表时间:
2018-12
影响因子:
2.6
通讯作者:
Huang Lili
中科院分区:
文献类型:
--
作者:
Zhou Feng;Qian Zhida;Huang Lili
PurposeTo investigate the molecular mechanisms governing aquaporin-1 (AQP1)-mediated, mifepristone-induced angiogenesis and improve the understanding of low-dose mifepristone serving as an anti-implantation contraceptive drug.MethodsHuman umbilical vein endothelial cells (HUVECs) were used to explore the effects of different concentrations of mifepristone (0, 65, and 200 nmol/L) on the activity of angiogenesis. Forty-five pregnant mice during the “window of implantation” were treated with different concentrations of mifepristone. HUVECs’ proliferation was examined using a methyl thiazolyl tetrazolium (MTT) assay. The microvessel density (MVD) and the expression of AQP1 in endometrium were determined with immunohistochemical methods.ResultsThe MVD and the expression of AQP1 were significantly higher than controls. Mifepristone at 200 nmol/L significantly affected HUVECs’ proliferation during culture over 12 h, and pretreatment with AQP1-specific siRNA significantly inhibited the mifepristone-enhanced cell proliferation.ConclusionsLow-dose mifepristone increased angiogenesis in a manner involving AQP1. This affords a new insight into the molecular mechanism underpinning the angiogenic effects of low-dose mifepristone.
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DOI:
--
发表时间:
1991
期刊:
Allergie und Immunologie
影响因子:
--
作者:
H. Weichert;I. Blechschmidt;S. Schröder;H. Ambrosius
通讯作者:
H. Weichert;I. Blechschmidt;S. Schröder;H. Ambrosius
DOI:
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1976-10
期刊:
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影响因子:
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作者:
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158.5
作者:
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通讯作者:
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DOI:
10.1097/01.gco.0000175362.12470.e0
发表时间:
2005-08
影响因子:
2.1
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DOI:
10.1097/gme.0b013e31816086ef
发表时间:
2008-07-01
影响因子:
2.7
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通讯作者:
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