Jazi Marie Saghaeian, Najafi Seyed Mahmoud Arab
Department of Molecular Medicine, Golestan University of Medial Sciences, Gorgan, Iran.
Department of Cell and Molecular Biology, School of Biology, Tehran University, Tehran, Iran.
Iran J Med Sci. 2017 Jan;42(1):66-72.
The canonical Wnt signal transduction (or the Wnt/β-catenin pathway) plays a crucial role in the development of animals and in carcinogenesis. Beta-catenin is the central component of this signaling pathway. The activation of Wnt/β-catenin signaling results in the cytoplasmic and nuclear accumulation of β-catenin. In the nucleus, β-catenin interacts with the TCF/LEF transcription factors and, therefore, participates in the upregulation or downregulation of some important genes involved in diverse cellular activities. In addition, β-catenin is a critical component of the cadherin-mediated cell adherens junction. We had previously noticed that very high cellular concentrations of β-catenin had a negative effect on the transcriptional activity of this protein and, therefore, the aim of this study was to find a mechanism for this negative interaction.
Cell fractionation, western blotting, and immunofluorescence microscopy experiments were performed to measure β-catenin protein levels and β-catenin cellular localization in HEK293Tcells transfected with various amounts of a β-catenin-encoding plasmid. Also, total RNA was extracted from the cells and used for reverse transcriptase-PCR experiments to measure the expression of the β-catenin target genes. SPSS, version 16, was used to analyze the results statistically.
We demonstrated that overexpression of β-catenin led to the formation of rod-shaped protein aggregates. The aggregate structures were mainly formed in the cell nucleus and were heavy enough to be isolated by centrifugation. Beta-catenin aggregate formation was accompanied by a decrease in the expression of the β-catenin target genes used in this study.
Since deregulation of β-catenin function occurs in several human diseases, including cancer and neurological disorders, the results of this paper further support the possible biological and clinical significance of β-catenin aggregate formation.
经典Wnt信号转导(即Wnt/β-连环蛋白途径)在动物发育和致癌过程中起着至关重要的作用。β-连环蛋白是该信号通路的核心成分。Wnt/β-连环蛋白信号的激活导致β-连环蛋白在细胞质和细胞核中积累。在细胞核中,β-连环蛋白与TCF/LEF转录因子相互作用,从而参与一些参与多种细胞活动的重要基因的上调或下调。此外,β-连环蛋白是钙黏蛋白介导的细胞黏附连接的关键成分。我们之前注意到细胞内β-连环蛋白浓度过高会对该蛋白的转录活性产生负面影响,因此,本研究的目的是找到这种负性相互作用的机制。
进行细胞分级分离、蛋白质免疫印迹和免疫荧光显微镜实验,以测量转染不同量β-连环蛋白编码质粒的HEK293T细胞中β-连环蛋白的蛋白水平和细胞定位。此外,从细胞中提取总RNA,用于逆转录聚合酶链反应实验,以测量β-连环蛋白靶基因的表达。使用SPSS 16版对结果进行统计学分析。
我们证明β-连环蛋白的过表达导致杆状蛋白聚集体的形成。聚集体结构主要在细胞核中形成,其重量足以通过离心分离。β-连环蛋白聚集体的形成伴随着本研究中使用的β-连环蛋白靶基因表达的降低。
由于β-连环蛋白功能失调发生在包括癌症和神经疾病在内的多种人类疾病中,本文的结果进一步支持了β-连环蛋白聚集体形成可能具有的生物学和临床意义。