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局灶性脑缺血后脑血管表达白细胞介素1β。

Cerebral vessels express interleukin 1beta after focal cerebral ischemia.

作者信息

Zhang Z, Chopp M, Goussev A, Powers C

机构信息

Henry Ford Health Sciences Center, Department of Neurology, Detroit, MI 48202, USA.

出版信息

Brain Res. 1998 Feb 16;784(1-2):210-7. doi: 10.1016/s0006-8993(97)01317-6.

Abstract

Rapid and marked increased levels of expression of interleukin 1beta (IL-1beta) mRNA have been detected in animal models of cerebral ischemia. However, the protein production of IL-1beta and the cellular sources of IL-1beta are largely undefined after cerebral ischemia. In the present study, we have measured the cellular localization of IL-1beta protein in brain tissue from non-ischemic and ischemic mice using immunohistochemistry. Male C57B/6J (n=45) mice were subjected to middle cerebral artery (MCA) occlusion by a clot or a suture. The mice were sacrificed at time points spanning the period from 15 min to 24 h after onset of the MCA occlusion. Non-operated and sham-operated mice were used as control groups. A monoclonal anti-IL-1beta antibody was used to detect IL-1beta. In the non-operated and sham-operated mice, a few IL-1beta immunoreactive cells were detected scattered throughout both hemispheres. IL-1beta immunoreactive cells increased in the ischemic lesion as early as 15 min and peaked at 1 h to 2 h after MCA occlusion. IL-1beta immunoreactivity was detected in the cortex of the contralateral hemisphere 1 h after ischemia. By 24 h after onset of ischemia, IL-1beta immunoreactivity was mainly present adjacent to the ischemic lesion and in the non-ischemic cortex. IL-1beta immunoreactivity was found on endothelial cells and microglia. This study demonstrates an early bilateral expression of IL-1beta on endothelium after MCA occlusion in mice.

摘要

在脑缺血动物模型中已检测到白细胞介素1β(IL-1β)mRNA的表达水平迅速且显著增加。然而,脑缺血后IL-1β的蛋白质产生及其细胞来源在很大程度上尚不清楚。在本研究中,我们使用免疫组织化学方法测量了非缺血和缺血小鼠脑组织中IL-1β蛋白的细胞定位。雄性C57B/6J(n = 45)小鼠通过血栓或缝线进行大脑中动脉(MCA)闭塞。在MCA闭塞开始后15分钟至24小时的时间点处死小鼠。未手术和假手术小鼠用作对照组。使用单克隆抗IL-1β抗体检测IL-1β。在未手术和假手术小鼠中,在整个两个半球中均检测到少数散在的IL-1β免疫反应性细胞。早在MCA闭塞后15分钟,缺血性病变中的IL-1β免疫反应性细胞就增加,并在1至2小时达到峰值。缺血后1小时在对侧半球的皮质中检测到IL-1β免疫反应性。到缺血开始后24小时,IL-1β免疫反应性主要存在于缺血性病变附近和非缺血性皮质中。在内皮细胞和小胶质细胞上发现了IL-1β免疫反应性。本研究证明了小鼠MCA闭塞后内皮上IL-1β的早期双侧表达。

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