Das Eashita, Jana Nihar Ranjan, Bhattacharyya Nitai Pada
Director, BioMedical Genomics Centre, PG Polyclinic (3rd Floor), 5 Suburban Hospital Road, Kolkata 700 020, India.
Microrna. 2015;4(2):86-100. doi: 10.2174/2211536604666150713105606.
Several indirect evidences are available to indicate that abnormalities in cell cycle may contribute to pathogenesis of Huntington's disease (HD). Here, we show that the cell cycle progression in STsdh(Q111)/Hdh(Q111)cells, a cell model of HD, is delayed in S and G2-M phases compared to control STHdhQ7/HdhQ7cells. Expression of 17 genes, like PCNA and CHEK1, was increased in STHdh(Q111)/Hdh(Q111)cells. Increased expressions of PCNA, CHEK1 and CCNA2, and an enhanced phosphorylation of Rb1 were observed in primary cortical neurons expressing mutant N-terminal huntingtin (HTT), R6/2 mice and STHdh(Q111)/Hdh(Q111) cells. This increase in the expressions of PCNA, CHEK1 and CCNA2 was found to be the result of decreased expressions of miR-432, miR-146a, and (miR-19a and miR-146a), respectively. Enhanced apoptosis was observed at late S phase and G2-M phase in STHdh(Q111)/Hdh(Q111)cells. Exogenous expressions of these miRNAs in STHdh(Q111)/Hdh(Q111) cells rescued the abnormalities in cell cycle and apoptosis. We also observed that inhibitors of cell cycle could decrease cell death in a cell model of HD. Based on these results obtained in cell and animal model of HD, we propose that inhibition of cell cycle either by miRNA expressions or by using inhibitors could be a potential approach for the treatment of HD.
有几个间接证据表明细胞周期异常可能与亨廷顿舞蹈症(HD)的发病机制有关。在此,我们发现HD细胞模型STsdh(Q111)/Hdh(Q111)细胞的细胞周期进程在S期和G2-M期比对照STHdhQ7/HdhQ7细胞延迟。PCNA和CHEK1等17个基因在STHdh(Q111)/Hdh(Q111)细胞中的表达增加。在表达突变型N端亨廷顿蛋白(HTT)的原代皮质神经元、R6/2小鼠和STHdh(Q111)/Hdh(Q111)细胞中,观察到PCNA、CHEK1和CCNA2的表达增加以及Rb1磷酸化增强。发现PCNA、CHEK1和CCNA2表达的增加分别是miR-432、miR-146a以及(miR-19a和miR-146a)表达降低的结果。在STHdh(Q111)/Hdh(Q111)细胞的S期晚期和G2-M期观察到凋亡增强。这些miRNA在STHdh(Q111)/Hdh(Q111)细胞中的外源性表达挽救了细胞周期和凋亡异常。我们还观察到细胞周期抑制剂可以减少HD细胞模型中的细胞死亡。基于在HD细胞和动物模型中获得的这些结果,我们提出通过miRNA表达或使用抑制剂抑制细胞周期可能是治疗HD的一种潜在方法。