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转录因子Sp1在阿尔茨海默病中的失调

Transcription factor Sp1 dysregulation in Alzheimer's disease.

作者信息

Citron Bruce A, Dennis John S, Zeitlin Ross S, Echeverria Valentina

机构信息

Laboratory of Molecular Biology, Research and Development 151, Bay Pines VA Healthcare System, Bay Pines, Florida 33744-4125, USA.

出版信息

J Neurosci Res. 2008 Aug 15;86(11):2499-504. doi: 10.1002/jnr.21695.

Abstract

Altered gene expression occurs in central nervous system disorders, including Alzheimer's disease (AD). Transcription factor Sp1 may be involved insofar as it can regulate the expression of several AD-related proteins, including amyloid precursor protein (APP) and tau. Sp1 could itself be regulated by inflammatory and other factors associated with AD, such as interleukin-1beta. We measured an almost threefold elevation in the number of mRNA molecules of this cytokine in the AD frontal cortex. Sp1 mRNA was found to be up-regulated in these AD brains (along with Sp1-regulated COX-2), and the Sp1 increase was also seen at the protein level by Western immunoblotting. To determine whether this would also occur in transgenic mice developing AD pathology, we examined the expression of Sp1 in the cortex and hippocampus and observed higher levels of Sp1 mRNA and protein. These results indicate that elements of regulatory pathways involving transcription factor Sp1 may be useful targets for therapeutic intervention to prevent or reverse AD.

摘要

基因表达改变发生在包括阿尔茨海默病(AD)在内的中枢神经系统疾病中。转录因子Sp1可能参与其中,因为它可以调节几种与AD相关蛋白质的表达,包括淀粉样前体蛋白(APP)和tau蛋白。Sp1本身可能受与AD相关的炎症及其他因素调控,如白细胞介素-1β。我们检测到在AD额叶皮质中这种细胞因子的mRNA分子数量几乎增加了两倍。在这些AD大脑中发现Sp1 mRNA上调(连同Sp1调节的COX-2),并且通过蛋白质免疫印迹在蛋白质水平上也观察到Sp1增加。为了确定这是否也会在发生AD病理变化的转基因小鼠中出现,我们检测了皮质和海马中Sp1的表达,观察到Sp1 mRNA和蛋白质水平较高。这些结果表明,涉及转录因子Sp1的调控途径元件可能是预防或逆转AD治疗干预的有用靶点。

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