Amyloid Beta Alters the Expression of microRNAs Regulating HMGCR and ABCA1 Genes in Astrocytes of C57BL/6J Mice.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Hossein Azizi Dariuni, Mehrnaz Karimi Darabi, Zahra Nazeri, Shirin Azizidoost, Alireza Kheiroallah, Azam Khedri, Maryam Cheraghzadeh
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引用次数: 0

Abstract

Dysregulation of brain cholesterol homeostasis causes the accumulation of extracellular protein deposits called amyloid plaques in the hippocampus which eventually leads to neuronal death, memory and learning deficits. The aim of the present study was to investigate the effect of beta amyloid on miRNAs regulating HMGCR and ABCA1 as cholesterol synthesis and homeostasis genes. Primary astrocytes were isolated from C57BL/6J mice, and were treated with 0.5 μM amyloid beta (Aβ). Expression levels of genes and miRNAs were measured by real-time PCR. In comparison to control, Aβ treatment resulted in a significant decrease in miR-96-5p expression as a positive and negative regulator of HMGCR and ABCA1, respectively. There was no significant increase in miR-27a-3p expression as a negative regulator of HMGCR. miR- 106b- 5p and miR-143-3p expressions were also dramatically decreased as ABCA1 negative regulators. Amyloid beta can alter the expression of major genes in the cholesterol homeostasis pathway via their regulatory miRNAs.

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β改变C57BL/6J小鼠星形胶质细胞中调节HMGCR和ABCA1基因的微小RNA的表达。
大脑胆固醇稳态的失调会导致海马体中被称为淀粉样蛋白斑块的细胞外蛋白质沉积的积累,最终导致神经元死亡、记忆和学习缺陷。本研究的目的是研究β淀粉样蛋白对作为胆固醇合成和稳态基因的调节HMGCR和ABCA1的miRNA的影响。从C57BL/6J小鼠中分离原代星形胶质细胞,并用0.5μM淀粉样蛋白β(Aβ)处理。通过实时PCR测量基因和miRNA的表达水平。与对照组相比,Aβ处理分别导致作为HMGCR和ABCA1的阳性和阴性调节因子的miR-96-5p表达显著降低。作为HMGCR的负调控因子,miR-27a-3p的表达没有显著增加。作为ABCA1负调控因子,miR-106b-5p和miR-143-3p的表达也显著降低。淀粉样蛋白β可以通过调节miRNA改变胆固醇稳态途径中主要基因的表达。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
0
期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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