| 共聚焦激光扫描显微镜研究大鼠脑缺血谷氨酸载体GLAST mRNA和EAAT1的表达与其细胞分布 |
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| 引用本文： | 黄娅林,晏义平,印克杰,孙凤艳. 共聚焦激光扫描显微镜研究大鼠脑缺血谷氨酸载体GLAST mRNA和EAAT1的表达与其细胞分布[J]. 中国临床神经科学, 2004, 12(2): 117-121 |
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| 作者姓名： | 黄娅林 晏义平 印克杰 孙凤艳 |
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| 作者单位： | 复旦大学上海医学院医学神经生物学国家重点实验室,200032 |
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| 基金项目： | 国家自然科学基金资助(No.30170301、30270479) |
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| 摘 要： | 目的通过应用共聚焦激光扫描显微镜技术(confocal laser scanning microscope, CLSM)观察脑缺血后谷氨酸载体GLAST mRNA和EAAT1蛋白表达的细胞定位,探讨CLSM技术中三维重建和三维显示在观察基因和蛋白在神经细胞上空间定位的应用.方法对脑缺血后采用原位杂交和免疫组织化学相结合的荧光双标技术标记的脑片进行双通道断层扫描以及三维数据重组.结果脑缺血后,荧光免疫组化双标显示大脑皮质缺血半暗区内的谷氨酸载体EAAT1蛋白与星形胶质细胞和神经元均有共表达;原位杂交结合免疫组化的荧光双标显示缺血周边区谷氨酸载体GLAST mRNA与星形胶质细胞和神经元有明显的共表达.结论共聚焦激光扫描显微镜观察脑缺血后谷氨酸载体GLAST mRNA和EAAT1蛋白在神经胶质细胞和神经元上的空间定位,为进一步研究脑缺血后谷氨酸载体系统作用机制提供了更为准确的形态依据.
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| 关 键 词： | 共聚焦激光扫描显微镜 双通道断层扫描和三维重建 荧光双标 原位杂交和免疫组织化学 谷氨酸载体GLAST mRNA EAAT1蛋白 脑缺血 |
| 文章编号： | 1008-0678(2004)02-0117-05 |
| 修稿时间： | 2004-03-12 |
Study on Cellular Localization of Glutamate Transporter GLAST mRNA and EAAT1 Protein Expression in Adult Rat after Cerebral Ischemia by Confocal Laser Scanning Microscopy |
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| HUANG Ya-Lin,YA Yi-Ping,YIN Ke-Jie,SUN Feng-Yan State Key Laboratory of Medical Neurobiology,Shanghai Medical College,Fudan University,Shanghai ,China. Study on Cellular Localization of Glutamate Transporter GLAST mRNA and EAAT1 Protein Expression in Adult Rat after Cerebral Ischemia by Confocal Laser Scanning Microscopy[J]. Chinese Journal of Clinical Neurosciences, 2004, 12(2): 117-121 |
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| Authors: | HUANG Ya-Lin YA Yi-Ping YIN Ke-Jie SUN Feng-Yan State Key Laboratory of Medical Neurobiology Shanghai Medical College Fudan University Shanghai China |
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| Affiliation: | HUANG Ya-Lin,YA Yi-Ping,YIN Ke-Jie,SUN Feng-Yan State Key Laboratory of Medical Neurobiology,Shanghai Medical College,Fudan University,Shanghai 200032,China |
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| Abstract: | Aim:Series and 3D image of confocal laser scanning microscopy(CLSM) combined with in situ hybridization and immuno-fluorescent double labeling techniques were used to study cellular localization of glutamate transporter GLAST mRNA and EAAT 1 protein expression in glial and neuronal cells of adult rat at 72 h following cerebral ischemia. Methods:After double labeling,expression of GLAST mRNA and EAAT 1 were detected in glial and neuronal cells of brain after ischemia injury by two channel scanning and 3D image of CLSM.Results:Double staining showed that glutamate transporter GLAST mRNA and EAAT 1 protein co-expressed with in some glial cells and neurons in the area penumbra of cerebral cortex.Conclusion:The results suggest that increase of GLAST mRNA and EAAT 1 protein expression in the area penumbra at 72 h postischemia possibly represent a protective mechanism for increasing extracelluar glutamate uptake and limiting glutamate neurotoxicity. Confocal laser scanning microscopy offered a real three-dimensional image for observing cellular localization of glutamate transporter GLAST mRNA and EAAT 1 protein expression in glial and neuronal cells of brain after ischemia injury. |
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| Keywords: | confocal laser scanning microscopy two channel and three-dimensional image in situ hybridization immunofluorescent double labeling glutamate transporter GLAST mRNA EAAT 1 protein cerebral ischemia |
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