Suppr超能文献

核因子κB在胚胎血管重塑和内皮-间充质转化过程中的潜在作用。

Possible role of NFkappaB in the embryonic vascular remodeling and the endothelial mesenchymal transition process.

作者信息

Arciniegas Enrique, Carrillo Luz M, De Sanctis Juan B, Candelle Daniel

机构信息

Facultad de Medicina, Servicio Autónomo Instituto de Biomedicina, Universidad Central de Venezuela, Caracas, Venezuela.

出版信息

Cell Adh Migr. 2008 Jan-Mar;2(1):17-29. doi: 10.4161/cam.2.1.5789. Epub 2008 Jan 23.

Abstract

The NFkappaB family of transcription factors, particularly the activated p50/p65 heterodimer, is expressed in vascular cells during intimal thickening formation when hemodynamic conditions are altered. Here, we report that p50, p65, IkappaBalpha and IKKalpha display different spatial and temporal patterns of expression and distribution during both chicken embryo aortic wall remodeling and intimal thickening development. Additionally, we show that both p50 and p65 were located in the nucleus of some mesenchymal cells expressing alpha-smooth muscle actin which are present in the spontaneous intimal thickening observed at embryonic days 12-14 of development. We also demonstrated that both NFkappaB subunits are present in monolayers of primary embryonic aortic endothelial cells attached to fibronectin and stimulated with complete medium. This study demonstrates for the first time the presence of activated NFkappaB during the remodeling of the embryonic aortic wall and the formation of intimal thickening, providing evidence that suggest a possible role for this transcription factor in the EndoMT process.

摘要

转录因子NFκB家族,尤其是活化的p50/p65异二聚体,在血流动力学条件改变时内膜增厚形成过程中在血管细胞中表达。在此,我们报道在鸡胚主动脉壁重塑和内膜增厚发育过程中,p50、p65、IκBα和IKKα呈现出不同的表达和分布时空模式。此外,我们发现p50和p65都位于一些表达α-平滑肌肌动蛋白的间充质细胞核内,这些间充质细胞存在于发育第12至14天观察到的自发性内膜增厚中。我们还证明,NFκB两个亚基都存在于附着于纤连蛋白并用完全培养基刺激的原代胚胎主动脉内皮细胞单层中。本研究首次证明在胚胎主动脉壁重塑和内膜增厚形成过程中存在活化的NFκB,为该转录因子在内皮-间充质转化过程中可能发挥的作用提供了证据。

相似文献

3
Intimal thickening involves transdifferentiation of embryonic endothelial cells.内膜增厚涉及胚胎内皮细胞的转分化。
Anat Rec. 2000 Jan 1;258(1):47-57. doi: 10.1002/(SICI)1097-0185(20000101)258:1<47::AID-AR6>3.0.CO;2-W.

引用本文的文献

8
"Venopathy" at work: recasting neointimal hyperplasia in a new light.静脉病变的作用:为内膜增生提供新视角。
Transl Res. 2010 Oct;156(4):216-25. doi: 10.1016/j.trsl.2010.07.004. Epub 2010 Aug 13.

本文引用的文献

2
3
Proinflammatory profile within the grossly normal aged human aortic wall.大体正常的老年人类主动脉壁内的促炎特征。
Hypertension. 2007 Jul;50(1):219-27. doi: 10.1161/HYPERTENSIONAHA.107.089409. Epub 2007 Apr 23.
5
Developmental basis of vascular smooth muscle diversity.血管平滑肌多样性的发育基础。
Arterioscler Thromb Vasc Biol. 2007 Jun;27(6):1248-58. doi: 10.1161/ATVBAHA.107.141069. Epub 2007 Mar 22.
8
Origin of neointimal smooth muscle: we've come full circle.新生内膜平滑肌的起源:我们又回到了原点。
Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2579-81. doi: 10.1161/01.ATV.0000249623.79871.bc.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验