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磁共振成像引导下对局灶性脑缺血大鼠模型中区域信号转导和转录激活因子1激活的研究

MR image-guided investigation of regional signal transducers and activators of transcription-1 activation in a rat model of focal cerebral ischemia.

作者信息

West D A, Valentim L M, Lythgoe M F, Stephanou A, Proctor E, van der Weerd L, Ordidge R J, Latchman D S, Gadian D G

机构信息

Royal College of Surgeons Unit of Biophysics, Institute of Child Health, University College London, London WC1N 1EH, UK.

出版信息

Neuroscience. 2004;127(2):333-9. doi: 10.1016/j.neuroscience.2004.05.022.

Abstract

BACKGROUND AND PURPOSE

STAT-1 is a member of a family of proteins called signal transducers and activators of transcription (STATs), and recent studies have shown its involvement in the induction of apoptosis. There is limited information on the role of STAT-1 following stroke. In this study we use MRI measurements of cerebral perfusion and bioenergetic status to target measurements of regional STAT-1 activity.

METHODS

Rats were subjected to 60 or 90 min of middle cerebral artery occlusion with and without reperfusion. MRI maps of the apparent diffusion coefficient of water and cerebral blood flow were acquired throughout the study. After the ischemia or reperfusion period, the brain was excised and samples were analyzed by Western blots using anti-phospho-STAT1 and anti-Fas antibodies. Regions were selected for analysis according to their MRI characteristics.

RESULTS

Transcriptional factor STAT-1 was enhanced in the lesion core and, to a lesser extent, in the lesion periphery, following ischemia and reperfusion. This level of activity was greater than for ischemia alone. Western blots demonstrated STAT-1 phosphorylation on tyrosine 701 and not serine 727 after ischemia and 3 h of reperfusion. Enhanced expression of the apoptotic death receptor Fas was confirmed after ischemia followed by reperfusion.

CONCLUSIONS

This study demonstrates that focal ischemia of the rat brain can induce STAT-1 activation, particularly following a period of reperfusion. The activation occurs not only in the lesion core, but also in the lesion periphery, as identified using MRI. STAT-1 may play an important role in the induction of cell death following stroke.

摘要

背景与目的

信号转导与转录激活因子(STATs)家族蛋白中的STAT-1,近期研究表明其参与细胞凋亡的诱导过程。关于中风后STAT-1的作用,相关信息有限。在本研究中,我们运用磁共振成像(MRI)测量脑灌注和生物能量状态,以靶向测量局部STAT-1活性。

方法

对大鼠进行60或90分钟大脑中动脉闭塞,部分伴有再灌注。在整个研究过程中获取水的表观扩散系数和脑血流量的MRI图谱。在缺血或再灌注期后,切除大脑并使用抗磷酸化STAT1和抗Fas抗体通过蛋白质免疫印迹法分析样本。根据MRI特征选择区域进行分析。

结果

在缺血和再灌注后,转录因子STAT-1在病变核心增强,在病变周边增强程度较小。这种活性水平高于单纯缺血时。蛋白质免疫印迹显示,缺血及再灌注3小时后,STAT-1在酪氨酸701而非丝氨酸727位点发生磷酸化。缺血后再灌注可证实凋亡死亡受体Fas的表达增强。

结论

本研究表明,大鼠脑局灶性缺血可诱导STAT-1激活,尤其是在一段再灌注期后。如通过MRI所确定的,激活不仅发生在病变核心,也发生在病变周边。STAT-1可能在中风后的细胞死亡诱导中起重要作用。

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