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[用于检测阿尔茨海默病转基因小鼠模型大脑中微小RNA差异表达的实时聚合酶链反应]

[Real-time PCR for detecting differential expressions of microRNAs in the brain of a transgenic mouse model of Alzheimer's disease].

作者信息

Tian Mi, Ding Yu, Hou Deren, Deng Yanyao, Li Wei, Feng Xialu

机构信息

Department of Neurology, Central South University, Changsha, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2013 Feb;33(2):262-6.

PMID:23443785
Abstract

OBJECTIVE

To detect the expression of miRNA-135a-5p, miRNA-135a-2-3p, miRNA-298-5p, miRNA-466b-3p and miR-669f-3p in the brain tissue of the APPswe/PS δE9 double transgenic mouse model of Alzheimer's disease using real-time PCR.

METHODS

Six-month-old APPswe/PS δE9 double transgenic mice and wild-type C57 mice of the same species were examined for the expressions of miRNA-135a-5p, miRNA-135a-2-3p, miRNA-298-5p, miRNA-466b-3p and miR-669f-3p in the brain tissue using real-time PCR.

RESULTS

The relative expression levels of the 5 miRNAs in the transgenic versus the wild-type mice were 0.73∓0.27 vs 1.08∓0.58, 2.47∓6.15 vs 1.65∓0.67, 0.72∓0.14 vs 1.31∓0.73, 0.57∓0.34 vs 1.06∓0.35, and 0.63∓0.26 vs 1.02∓0.18, respectively, showing significance differences in the expressions of miRNA-135a-5p, miRNA-298-5p, miRNA-466b-3p, and miR-669f-3p between the two groups (P<0.05).

CONCLUSIONS

miRNA-135a-5p, miRNA-298-5p, miRNA-466b-3p and miR-669f-3p are expressed differentially in APPswe/PS δE9 double transgenic mice, suggesting their important roles in the pathogenesis of Alzheimer disease.

摘要

目的

采用实时定量聚合酶链反应检测阿尔茨海默病APPswe/PSδE9双转基因小鼠模型脑组织中miRNA-135a-5p、miRNA-135a-2-3p、miRNA-298-5p、miRNA-466b-3p和miR-669f-3p的表达。

方法

运用实时定量聚合酶链反应检测6月龄APPswe/PSδE9双转基因小鼠和同品系野生型C57小鼠脑组织中miRNA-135a-5p、miRNA-135a-2-3p、miRNA-298-5p、miRNA-466b-3p和miR-669f-3p的表达。

结果

5种miRNA在转基因小鼠与野生型小鼠中的相对表达水平分别为0.73±0.27对1.08±0.58、2.47±6.15对1.65±0.67、0.72±0.14对1.31±0.73、0.57±0.34对1.06±0.35、0.63±0.26对1.02±0.18,两组间miRNA-135a-5p、miRNA-298-5p、miRNA-466b-3p和miR-669f-3p的表达存在显著差异(P<0.05)。

结论

miRNA-135a-5p、miRNA-298-5p、miRNA-466b-3p和miR-669f-3p在APPswe/PSδE9双转基因小鼠中表达存在差异,提示它们在阿尔茨海默病发病机制中发挥重要作用。

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