Literature DB >> 27113042

Folic Acid Protected Neural Cells Against Aluminum-Maltolate-Induced Apoptosis by Preventing miR-19 Downregulation.

Mingming Zhu1, Bingfei Li2, Xiao Ma1, Cong Huang1, Rui Wu1, Weiwei Zhu1, Xiaoting Li1, Zhaofeng Liang1, Feifei Deng1, Jianyun Zhu1, Wei Xie1, Xue Yang1, Ye Jiang1, Shijia Wang1, Jieshu Wu1, Shanshan Geng1, Chunfeng Xie1, Caiyun Zhong3, Haiyan Liu4.   

Abstract

Aluminum (Al)-induced apoptosis is considered as the major cause of its neurotoxicity. Folic acid possesses neuroprotective function by preventing neural cell apoptosis. microRNAs (miRNAs) are important regulators of gene expression participating in cellular processes. As a key component of the miR-17-92 cluster, miR-19 is implicated in regulating apoptotic process, while its role in the neuroprotective effect of folic acid has not been investigated. The present study aimed to investigate the potential involvement and function of miR-19 in the protective action of folic acid against Al-induced neural cell apoptosis. Human SH-SY5Y cells were treated with Al-maltolate (Al-malt) in the presence or absence of folic acid. Results showed that Al-malt-induced apoptosis of SH-SY5Y cells was effectively prevented by folic acid. Al-malt suppressed the expression of miR-19a/19b, along with alterations of miR-19 related apoptotic proteins including PTEN, p-AKT, p53, Bax, Bcl-2, caspase 9 and caspase 3; and these effects were ameliorated by folic acid. miR-19 inhibitor alone induced apoptosis of SH-SY5Y cells. Combination treatment of folic acid and miR-19 inhibitor diminished the neuroprotective effect of folic acid. These findings demonstrated that folic acid protected neuronal cells against Al-malt-induced apoptosis by preventing the downregulation of miR-19 and modulation of miR-19 related downstream PTEN/AKT/p53 pathway.

Entities:  

Keywords:  Aluminum; Apoptosis; Folic acid; Modulation; Neurodegenerative diseases; miR-19

Mesh:

Substances:

Year:  2016        PMID: 27113042     DOI: 10.1007/s11064-016-1926-9

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  45 in total

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