Suppr超能文献

骨形态发生蛋白-6在大鼠创伤性脑损伤病灶中由活化的星形胶质细胞早期表达。

Bone morphogenetic protein-6 is expressed early by activated astrocytes in lesions of rat traumatic brain injury.

作者信息

Zhang Z, Trautmann K, Artelt M, Burnet M, Schluesener H J

机构信息

Institute of Brain Research, University of Tuebingen, Calwer Str. 3, D-72076 Tuebingen, Germany.

出版信息

Neuroscience. 2006;138(1):47-53. doi: 10.1016/j.neuroscience.2005.11.036. Epub 2006 Jan 4.

Abstract

We have analyzed early expression of bone morphogenetic protein-6 in rat brains subjected to traumatic brain injury. Bone morphogenetic protein-6 was expressed in neurons of the hippocampus and cortex in normal adult rat brains. A pronounced expression of bone morphogenetic protein-6 in astroglia located to the lesion became obvious 48 h postinjury. Bone morphogenetic protein-6(+) glia were distributed around the lesion, thus demarcating the injured tissue from normal brain. Double labeling by immunohistochemistry revealed that the major glial sources for bone morphogenetic protein-6 were reactive astrocytes and few ED1(+) or W3/13(+) cells co-expressed bone morphogenetic protein-6. Furthermore, bone morphogenetic protein-6 expression in neurons located to hippocampus and cortex of the lesioned hemisphere was up-regulated 3 days postinjury. In conclusion, this is the first description of bone morphogenetic protein-6 expression in traumatic brains. Our data suggest that bone morphogenetic protein-6 might be involved in astrogliosis and neuron protection following traumatic brain injury.

摘要

我们分析了创伤性脑损伤大鼠脑中骨形态发生蛋白-6的早期表达情况。在正常成年大鼠脑中,骨形态发生蛋白-6在海马体和皮质的神经元中表达。损伤后48小时,位于损伤部位的星形胶质细胞中骨形态发生蛋白-6出现明显表达。骨形态发生蛋白-6阳性胶质细胞分布在损伤部位周围,从而将损伤组织与正常脑组织区分开来。免疫组织化学双重标记显示,骨形态发生蛋白-6的主要胶质细胞来源是反应性星形胶质细胞,少数ED1阳性或W3/13阳性细胞也共表达骨形态发生蛋白-6。此外,损伤后3天,损伤半球海马体和皮质中的神经元中骨形态发生蛋白-6的表达上调。总之,这是首次对创伤性脑损伤中骨形态发生蛋白-6表达的描述。我们的数据表明,骨形态发生蛋白-6可能参与创伤性脑损伤后的星形胶质细胞增生和神经元保护。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验