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Höchstauflösendes Fluoreszenzmikroskop

Höchstauflösendes Fluoreszenzmikroskop
高分辨率荧光显微镜
批准号:
260348792
负责人:
金额:
$0.0万
依托单位国家:
德国
项目类别:
Major Research Instrumentation
财政年份:
2014
资助国家:
德国
项目状态:
未结题
起止时间:
2013-12-31 至 --

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中文摘要
翻译
为了确定治疗疾病的新策略,具有纳米级分辨率的先进成像策略对于揭示生理环境中健康和患病细胞和组织的细胞内和细胞外过程以及过程的形态是必不可少的。目前可用的光学显微镜技术和基础科学的其他成像模式要么不适用于研究可行的样品,要么不提供获得疾病过程的细胞内环境(< 100 nm)的分辨率。因此,我们的目标是获得和采用最先进的“三维受激发射耗尽”(STED X3)显微镜。STED将使我们能够获得与疾病相关的结构和功能过程的超详细信息,特别是心血管发病机制。STED在活细胞或组织中的适用性及其纳米级分辨率将揭示致病背景下的新机制和迄今为止不可见的结构。这将有助于更好地了解和治疗疾病。
英文摘要
To identify new strategies for the treatment of disease, advanced imaging strategies with nanoscale resolution are essential to reveal intra- and extracellular processes and the morphology of processes of healthy and diseased cells and tissues in a physiological environment. The currently available optical microscopic techniques and other imaging modalities for basic science are either not applicable to study viable samples or do not offer the resolution for gaining access to the intracellular environment (< 100 nm) of disease processes. We therefore aim to obtain and employ the state-of-the-art "three dimensional stimulated emission depletion" (STED X3) microscopy. STED will enable us to acquire ultra-detailed information on structural and functional processes relevant to disease, in particular cardiovascular pathogenesis. The applicability of STED in live cells or tissues combined with its nanoscale resolution will unravel new mechanisms and hitherto invisible structures in a pathogenic context. This will contribute to a better understanding and treatment of disease.
期刊论文(8)
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会议论文
DOI: 10.1160/th17-04-0302
发表时间: 2018-02-01
期刊: THROMBOSIS AND HAEMOSTASIS
影响因子: 6.7
作者: [Ebrahim, Mariam, Jamasbi, Janina, Siess, Wolfgang]
通讯作者: Siess, Wolfgang
CD27 co-stimulation increases the abundance of regulatory T cells and reduces atherosclerosis in hyperlipidaemic mice
CD27 共刺激可增加高脂血症小鼠调节性 T 细胞的丰度并减少动脉粥样硬化
DOI: 10.1093/eurheartj/ehx517
发表时间: 2017
期刊: European Heart Journal
影响因子: 39.3
作者: [Winkels H, Meiler S, Lievens D, Engel D, Spitz C, Bürger C, Beckers L, Dandl A, Reim S, Ahmadsei M, Hartwig H, Holdt LM, Hristov M, Megens RTA, Schmitt MM, Biessen EA, Borst J, Faussner A, Weber C, Lutgens E, Gerdes N]
通讯作者: Gerdes N
Optical imaging innovations for atherosclerosis research: multiphoton microscopy and optical nanoscopy.
动脉粥样硬化研究的光学成像创新:多光子显微镜和光学纳米显微镜
DOI: 10.1161/atvbaha.115.304875
发表时间: 2015
期刊: Arteriosclerosis, Thrombosis, & Vascular Biology
影响因子: --
作者: [Megens RTA, Bianchini M, Schmitt MNN, Weber C]
通讯作者: Weber C
DOI: 10.1160/th16-04-0318
发表时间: 2016-10
期刊: Thrombosis and Haemostasis
影响因子: 6.7
作者: [H. Winkels;Svenja Meiler;E. Smeets;D. Lievens;D. Engel;Charlotte Spitz;C. Bürger;P. Rinne;Linda Beckers;Angelika Dandl;S. Reim;M. Ahmadsei;J. van den Bossche;L. Holdt;R. Megens;Martin M. N. Schmitt;M. D. de Winther;E. Biessen;J. Borst;A. Faussner;C. Weber;E. Lutgens;N. Gerdes]
通讯作者: H. Winkels;Svenja Meiler;E. Smeets;D. Lievens;D. Engel;Charlotte Spitz;C. Bürger;P. Rinne;Linda Beckers;Angelika Dandl;S. Reim;M. Ahmadsei;J. van den Bossche;L. Holdt;R. Megens;Martin M. N. Schmitt;M. D. de Winther;E. Biessen;J. Borst;A. Faussner;C. Weber;E. Lutgens;N. Gerdes
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