...
首页> 外文期刊>Brain research. Molecular brain research >Accumulation of the amyloid precursor-like protein APLP2 and reduction of APLP1 in retinoic acid-differentiated human neuroblastoma cells upon curcumin-induced neurite retraction.
【24h】

Accumulation of the amyloid precursor-like protein APLP2 and reduction of APLP1 in retinoic acid-differentiated human neuroblastoma cells upon curcumin-induced neurite retraction.

机译:姜黄素诱导的神经突收缩后,视黄酸分化的人神经母细胞瘤细胞中淀粉样前体样蛋白APLP2的积累和APLP1的减少。

获取原文
获取原文并翻译 | 示例
           

摘要

Amyloid precursor protein (APP) belongs to a conserved gene family, also including the amyloid precursor-like proteins, APLP1 and APLP2. The function of these three proteins is not yet fully understood. One of the proposed roles of APP is to promote neurite outgrowth. The aim of this study was to investigate the regulation of the expression levels of APP family members during neurite outgrowth. We observed that retinoic acid (RA)-induced neuronal differentiation of human SH-SY5Y cells resulted in increased expression of APP, APLP1 and APLP2. We also examined the effect of the NFkappaB, AP-1 and c-Jun N-terminal kinase inhibitor curcumin (diferuloylmethane) on the RA-induced expression levels of these proteins. We found that treatment with curcumin counteracted the RA-induced mRNA expression of all APP family members. In addition, we observed that curcumin treatment resulted in neurite retraction without any effect on cell viability. Surprisingly, curcumin had differential effects on the APLP protein levels in RA-differentiated cells. RA-induced APLP1 protein expression was blocked by curcumin, while the APLP2 protein levels were further increased. APP protein levels were not affected by curcumin treatment. We propose that the sustained levels of APP and the elevated levels of APLP2, in spite of the reduced mRNA expression, are due to altered proteolytic processing of these proteins. Furthermore, our results suggest that APLP1 does not undergo the same type of regulated processing as APP and APLP2.
机译:淀粉样前体蛋白(APP)属于保守的基因家族,也包括淀粉样前体样蛋白APLP1和APLP2。这三种蛋白质的功能尚未完全了解。 APP的拟议作用之一是促进神经突增生。这项研究的目的是调查神经突生长过程中APP家族成员表达水平的调节。我们观察到视黄酸(RA)诱导人SH-SY5Y细胞的神经元分化导致APP,APLP1和APLP2的表达增加。我们还检查了NFkappaB,AP-1和c-Jun N端激酶抑制剂姜黄素(二氟甲酰甲烷)对RA诱导的这些蛋白表达水平的影响。我们发现用姜黄素治疗可以抵消RA诱导的所有APP家族成员的mRNA表达。此外,我们观察到姜黄素治疗可导致神经突回缩,而对细胞活力没有任何影响。出乎意料的是,姜黄素对RA分化细胞中APLP蛋白水平具有不同的影响。姜黄素可阻断RA诱导的APLP1蛋白表达,而APLP2蛋白水平则进一步升高。姜黄素治疗不影响APP蛋白水平。我们建议,尽管mRNA的表达降低,但APP的持续水平和APLP2的水平升高是由于这些蛋白的蛋白水解过程改变所致。此外,我们的结果表明,APLP1与APP和APLP2不会经历相同类型的调节处理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号