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内皮糖蛋白抑制通过激活与COUP-TFII信号通路相关的因子导致套叠式血管生成。

Endoglin inhibition leads to intussusceptive angiogenesis via activation of factors related to COUP-TFII signaling pathway.

作者信息

Hlushchuk Ruslan, Styp-Rekowska Beata, Dzambazi Jehona, Wnuk Monika, Huynh-Do Uyen, Makanya Andrew, Djonov Valentin

机构信息

Institute of Anatomy, University of Bern, Bern, Switzerland.

Department of Nephrology and Hypertension, Inselspital Bern, Bern, Switzerland.

出版信息

PLoS One. 2017 Aug 31;12(8):e0182813. doi: 10.1371/journal.pone.0182813. eCollection 2017.

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.

摘要

血管生成是一个由多种信号分子和血流状况精心调控的高度协调且极其复杂的过程。虽然血管生成的芽生模式已得到充分研究,但作为血管生成的第二种模式的套叠式血管生成的分子机制仍 largely 不清楚。在当前研究中,对参与血管生长和分化的两个分子,即内皮糖蛋白(ENG/CD105)和鸡卵清蛋白上游启动子转录因子 II(COUP-TFII)进行了研究,以阐明它们在血管生成中的具体作用。这两个分子的下调和上调分别与套叠式微血管生长紧密相关。在鸡胚模型中抑制 ENG 后,可以观察到不规则毛细血管网的形成,同时伴有 COUP-TFII 表达增加。ENG 和 COUP-TFII 在血管发育和重塑过程中的这种动态表达模式与柱的形成和套叠式血管生成的进展相关。在急性大鼠 Thy1.1 肾小球肾炎的哺乳动物模型中也观察到了类似的结果,该模型通过静脉注射抗 Thy1 抗体诱导,在套叠式血管生成的初始阶段显示 COUP-TFII 上调,而与对照组相比,ENG 表达未受干扰,但在柱形成过程中随时间下降。在本研究中,我们表明抑制 ENG 并同时上调 COUP-TFII 表达可促进套叠式血管生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c70c/5578572/c5103902fa80/pone.0182813.g001.jpg

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