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在体光学成像检测短暂性脑缺血后早期脑内细胞凋亡

In vivo optical imaging of early-stage apoptosis in mouse brain after transient cerebral ischemia.

机构信息

Department of Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

出版信息

J Neurosci Res. 2010 Dec;88(16):3488-97. doi: 10.1002/jnr.22489. Epub 2010 Oct 8.

DOI:10.1002/jnr.22489
PMID:20936709
Abstract

Apoptosis is one of the mechanisms contributing to neuronal degeneration in ischemic stroke. In vivo imaging of annexin V (A5) was performed at 12 hr, 24 hr, 48 hr, and 4 days after 90-min transient middle cerebral artery occlusion (tMCAO) in mice with a fluorescent protein Cy5.5. Immunohistochemistry for heat shock protein 70 (HSP70), A5, and TUNEL were also performed with brain sections after the tMCAO. In vivo fluorescence was strongly observed at 48 hr over the head, especially with removal of both head skin and skull bone. Zonal ex vivo fluorescent signals were surrounding the ischemic core, and double-positive cells with Cy5.5/exogenous A5 antibody were found in this area. HSP70 was observed at the peak time of 24 hr; A5 became detectable at 12 hr, with increasing numbers until 48 hr. The number of TUNEL-positive cells increased at 24 hr and retained the high level until 4 days, showing a dissociating temporal pattern with A5. Double-positive cells for A5/TUNEL reached their peak at 48 hr. All the data suggest that some cells still have a chance to be rescued for a long period after acute cerebral ischemia. The in vivo Cy5.5 fluorescence representing A5 signal spatially surrounding the ischemic core temporally detects an early-stage apoptosis after cerebral ischemia.

摘要

细胞凋亡是导致缺血性脑卒中神经元变性的机制之一。使用荧光蛋白 Cy5.5 在经过 90 分钟短暂性大脑中动脉闭塞(tMCAO)后的 12 小时、24 小时、48 小时和 4 天对小鼠进行了膜联蛋白 V(A5)的体内成像。在 tMCAO 后,还对脑切片进行了热休克蛋白 70(HSP70)、A5 和 TUNEL 的免疫组织化学染色。在头部的 48 小时可以强烈观察到体内荧光,尤其是在去除头部皮肤和颅骨后。体外荧光信号在缺血核心周围呈带状分布,在该区域发现了 Cy5.5/外源性 A5 抗体的双阳性细胞。HSP70 在 24 小时达到峰值;A5 在 12 小时可检测到,直到 48 小时数量不断增加。TUNEL 阳性细胞的数量在 24 小时增加,并在 4 天内保持高水平,与 A5 呈分离的时间模式。A5/TUNEL 的双阳性细胞在 48 小时达到峰值。所有数据表明,在急性脑缺血后很长一段时间内,仍有一些细胞有机会得到挽救。体内 Cy5.5 荧光代表 A5 信号在缺血核心周围的时空分布,可在脑缺血后早期检测到细胞凋亡。

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