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在体局部缺血小鼠模型中脑血管壁的无标记二次谐波产生成像。

Label-free second harmonic generation imaging of cerebral vascular wall in local ischemia mouse model in vivo.

机构信息

School of Life Sciences, State Key Laboratory of Medical Neurobiology, Collaborative Innovation Center for Brain Science, Fudan University, 2005 Songhu Road, Shanghai 200438, China.

Key Laboratory of OptoElectronic Science and Technology for Medicine of Ministry of Education, Fujian Provincial Key Laboratory of Photonics Technology, Fujian Normal University, Fuzhou 350007, China.

出版信息

Neuroscience. 2022 Oct 15;502:10-24. doi: 10.1016/j.neuroscience.2022.08.003. Epub 2022 Aug 30.

Abstract

Second harmonic generation (SHG) imaging is label-free and non-invasive, and it has been extensively applied in multiple biological and medical studies, but not in the brain in vivo. In this study, we modified classical two photon excited fluorescence (TPEF) system to perform in vivo simultaneous TPEF and SHG imaging in the local ischemia mouse model. In cerebral vascular walls, we found strong SHG signal, which co-localized with collagen. In the continuous 2 days' in vivo imaging, this SHG signal remained stable in the local ischemic blood vessel in the initial 4 h, then its signal abruptly increased and got spatially thickened 5 h after thrombosis, and this tendency continued in the following 48 h. This study provides direct and precise timeline of rapid collagen change in cerebral vascular walls in vivo, and reveals the subtle but significant temporal-spatial dynamics of this structural signal during local ischemia. Thus, this cerebral in vivo SHG imaging provides a powerful tool to identify the early and subtle pathological change of collagen around clinical key therapeutic time window.

摘要

二次谐波产生(SHG)成像无标记且非侵入性,已广泛应用于多项生物学和医学研究,但尚未应用于活体大脑。在这项研究中,我们对经典的双光子激发荧光(TPEF)系统进行了修改,以在局部缺血小鼠模型中进行体内同时 TPEF 和 SHG 成像。在脑血管壁中,我们发现了强烈的 SHG 信号,该信号与胶原蛋白共定位。在连续 2 天的体内成像中,在最初的 4 小时内,局部缺血血管中的 SHG 信号保持稳定,然后在血栓形成后 5 小时信号突然增加且空间变厚,并且这种趋势在接下来的 48 小时内持续。这项研究提供了活体脑血管壁中胶原蛋白快速变化的直接而精确的时间轴,并揭示了局部缺血过程中这种结构信号的微妙但显著的时空动力学。因此,这种脑内 SHG 成像为识别临床关键治疗时间窗周围胶原蛋白的早期和细微病理变化提供了有力工具。

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