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病态肥胖中国女性皮下脂肪组织中的微小RNA表达谱

MicroRNA Expression Profiles in the Subcutaneous Adipose Tissues of Morbidly Obese Chinese Women.

作者信息

Wang Linjie, Shang Chen, Pan Hui, Yang Hongbo, Zhu Huijuan, Gong Fengying

机构信息

Key Laboratory of Endocrinology of National Health Commission, Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

Key Laboratory of Endocrinology of National Health Commission, Department of Endocrinology, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China,

出版信息

Obes Facts. 2021 Feb 5;14(1):1-15. doi: 10.1159/000511772.

Abstract

INTRODUCTION

Obesity is a main global health issue and an outstanding cause of morbidity and mortality. Exploring miRNA profiling may help further studies on obesity.

METHODS

Three morbidly obese and 5 normal-weight Chinese women were enrolled in the microarray testing group. Abdominal subcutaneous adipose tissue (SAT) samples were excised. Total RNAs including miRNAs were extracted. Affymetrix GeneChip miRNA 4.0 Array was used to compare the expression profiles of miRNAs between the 2 groups. Two algorithms, miRanda and TargetScan, were used to predict target messenger RNAs (mRNAs). Bioinformatics analysis was then done based on the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. The sample sizes were further expanded to 8 morbidly obese and 9 normal-weight subjects, and quantitative real-time PCR (qRT-PCR) was utilized to verify the expression of differential miRNAs and target genes.

RESULTS

As per the microarray assay, 58 miRNAs were differentially expressed in the SAT from the morbidly obese and normal-weight groups (Fold >4, p < 0.01, FDR <0.05); 54 of these were downregulated and 4 were upregulated in morbidly obese subjects. A total of 1,333 target genes were jointly predicted by miRanda and TargetScan. Further bioinformatics analysis showed that the differential miRNAs were involved in 269 significant biological functions and 89 significant signaling pathways. The validation experiment by qRT-PCR showed that the expression levels of miRNA-143-5p, miRNA-143-3p, miRNA-145-5p, and let-7a-5p were downregulated in morbidly obese subjects, consistent with the microarray detection. High-mobility group A2 (HMGA2), a target gene of the downregulated miRNA let-7a-5p, was first found to be upregulated 3.19-fold in the SAT of morbidly obese Chinese women when compared to normal-weight controls.

CONCLUSIONS

MiRNA downregulation is a hallmark of intact SAT in a morbidly obese state. Transcription (DNA-dependent), small-molecule metabolic processes, the MAPK signaling pathway, and cancer-related pathways may play important roles in the occurrence and development of obesity. For the first time, we proved that HMGA2, a target gene of let-7a-5p, is upregulated in the SAT of morbidly obese Chinese women.

摘要

引言

肥胖是一个主要的全球健康问题,也是发病和死亡的一个突出原因。探索微小RNA(miRNA)谱可能有助于肥胖症的进一步研究。

方法

选取3名病态肥胖和5名体重正常的中国女性纳入微阵列检测组。切除腹部皮下脂肪组织(SAT)样本。提取包括miRNA在内的总RNA。使用Affymetrix GeneChip miRNA 4.0阵列比较两组之间miRNA的表达谱。使用miRanda和TargetScan两种算法预测靶信使核糖核酸(mRNA)。然后基于基因本体论(GO)和京都基因与基因组百科全书(KEGG)数据库进行生物信息学分析。样本量进一步扩大至8名病态肥胖和9名体重正常的受试者,并利用定量实时聚合酶链反应(qRT-PCR)验证差异miRNA和靶基因的表达。

结果

根据微阵列分析,58种miRNA在病态肥胖组和体重正常组的SAT中差异表达(倍数变化>4,p<0.01,错误发现率<0.05);其中54种在病态肥胖受试者中下调,4种上调。miRanda和TargetScan共同预测了总共1333个靶基因。进一步的生物信息学分析表明,差异miRNA参与了269种重要生物学功能和89条重要信号通路。qRT-PCR验证实验表明,miRNA-143-5p、miRNA-143-3p、miRNA-145-5p和let-7a-5p在病态肥胖受试者中的表达水平下调,与微阵列检测结果一致。首次发现,与体重正常的对照组相比,下调的miRNA let-7a-5p的靶基因高迁移率族蛋白A2(HMGA2)在病态肥胖中国女性的SAT中上调3.19倍。

结论

miRNA下调是病态肥胖状态下完整SAT的一个标志。转录(DNA依赖性)、小分子代谢过程、丝裂原活化蛋白激酶(MAPK)信号通路和癌症相关通路可能在肥胖的发生和发展中起重要作用。我们首次证明,let-7a-5p的靶基因HMGA2在病态肥胖中国女性的SAT中上调。

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