Suppr超能文献

转录因子渗透压反应增强子结合蛋白(TonEBP)可反式激活渗透保护基因,在脑部神经元急性全身性高渗状态后表达并上调。

Transcription factor tonicity-responsive enhancer-binding protein (TonEBP) which transactivates osmoprotective genes is expressed and upregulated following acute systemic hypertonicity in neurons in brain.

作者信息

Loyher M L, Mutin M, Woo S K, Kwon H M, Tappaz M L

机构信息

Unité INSERM 433, Neurobiologie Experimentale et Physiopathologie, Faculté de Médecine RTH Laennec, Rue Guillaume Paradin, F 69372 Lyon, Cedex 08, France.

出版信息

Neuroscience. 2004;124(1):89-104. doi: 10.1016/j.neuroscience.2003.10.025.

Abstract

Tonicity-responsive enhancer-binding protein (TonEBP) was initially identified as a transcription factor involved in adaptation of renal cells to hypertonicity by activation of osmoprotective genes encoding proteins for accumulation of compatible osmolytes. Since brain osmoadaptation is observed in relationship to neurological disorders resulting from pathological osmotic disbalances of blood plasma we have investigated through immunocytochemistry TonEBP expression in cerebral cortex and hippocampus of normal rat and rats submitted to an acute systemic hypertonicity or to a prolonged systemic hypotonicity. TonEBP-expressing cells were identified using double immunofluorescence and appropriate cell type markers. Their relative proportion was determined by quantitative image analysis. In normal rats TonEBP expressed primarily in neurons where it was strictly located in the cell nucleus but heterogeneously distributed into a nucleoplasmic pool and a granular pool. In animals made acutely hypertonic TonEBP labeling increased dramatically exclusively in the nuclei of neurons and reached a maximum within 1 h. In hypertonic animals TonEBP labeling covered the whole cell nucleus of virtually all neurons, appeared finely punctuated but was no more granular. Optical density of the labeling as determined by image analysis correlated linearly with the increased plasma osmolality. In animals made hypotonic for several days no conspicuous decrease of TonEBP labeling was observed. In normal animals a very minor proportion of non-neuronal cells showed a faint TonEBP nuclear labeling. This proportion increased slightly in hypertonic animals. Nevertheless these non-neuronal TonEBP-positive nuclei which belonged to oligodendrocytes and to a small subpopulation of astrocytes remained always very weakly labeled when compared with neuron nuclei. Brain capillary endothelial cells as well as microglial cells showed no TonEBP-labeling even in hypertonic animals. Our data demonstrate that in brain TonEBP is significantly expressed and tonicity-overexpressed in neurons and accordingly suggest that neurons only among brain cells accumulate compatible osmolytes through TonEBP-mediated activation of osmoprotective genes to adapt to acute systemic hypertonicity.

摘要

张力反应增强子结合蛋白(TonEBP)最初被鉴定为一种转录因子,它通过激活编码相容性渗透溶质积累相关蛋白质的渗透保护基因,参与肾细胞对高渗环境的适应。由于在因血浆病理性渗透压失衡导致的神经疾病中观察到脑渗透压适应现象,我们通过免疫细胞化学方法研究了正常大鼠以及经历急性全身性高渗或长期全身性低渗的大鼠大脑皮层和海马中TonEBP的表达情况。使用双重免疫荧光和适当的细胞类型标记物来鉴定表达TonEBP的细胞。通过定量图像分析确定它们的相对比例。在正常大鼠中,TonEBP主要在神经元中表达,且严格定位于细胞核内,但不均匀地分布在核质池和颗粒池中。在急性高渗动物中,TonEBP标记仅在神经元核中急剧增加,并在1小时内达到最大值。在高渗动物中,TonEBP标记几乎覆盖了所有神经元的整个细胞核,呈细点状,但不再呈颗粒状。通过图像分析确定的标记光密度与血浆渗透压的升高呈线性相关。在低渗处理数天的动物中,未观察到TonEBP标记的明显减少。在正常动物中,非常小比例的非神经元细胞显示出微弱的TonEBP核标记。在高渗动物中,这一比例略有增加。然而,与神经元核相比,这些属于少突胶质细胞和一小部分星形胶质细胞的非神经元TonEBP阳性核的标记始终非常微弱。即使在高渗动物中,脑毛细血管内皮细胞和小胶质细胞也未显示出TonEBP标记。我们的数据表明,在大脑中,TonEBP在神经元中显著表达且对张力过度表达,因此表明在脑细胞中只有神经元通过TonEBP介导的渗透保护基因激活来积累相容性渗透溶质,以适应急性全身性高渗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验