Cell-Specific Dysregulation of MicroRNA Expression in Obese White Adipose Tissue

小RNA 基质血管部分 脂肪组织 生物 转录组 白色脂肪组织 间质细胞 细胞生物学 基因表达调控 基因表达 内分泌学 癌症研究 基因 遗传学
作者
Frédérik Oger,Céline Gheeraert,Denis A. Mogilenko,Yacir Benomar,Olivier Molendi‐Coste,Emmanuel Bouchaert,Sandrine Caron,David Dombrowicz,François Pattou,Hélène Duez,Jérôme Eeckhoute,Bart Staels,Philippe Lefèbvre
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [The Endocrine Society]
卷期号:99 (8): 2821-2833 被引量:61
标识
DOI:10.1210/jc.2013-4259
摘要

Obesity is characterized by the excessive accumulation of dysfunctional white adipose tissue (WAT), leading to a strong perturbation of metabolic regulations. However, the molecular events underlying this process are not fully understood.MicroRNAs (miRNAs) are small noncoding RNAs acting as posttranscriptional regulators of gene expression in multiple tissues and organs. However, their expression and roles in WAT cell subtypes, which include not only adipocytes but also immune, endothelial, and mesenchymal stem cells as well as preadipocytes, have not been characterized. Design/Results: By applying differential miRNome analysis, we demonstrate that the expression of several miRNAs is dysregulated in epididymal WAT from ob/ob and high-fat diet-fed mice. Adipose tissue-specific down-regulation of miR-200a and miR-200b and the up-regulation of miR-342-3p, miR-335-5p, and miR-335-3p were observed. Importantly, a similarly altered expression of miR-200a and miR-200b was observed in obese diabetic patients. Furthermore, cell fractionation of mouse adipose tissue revealed that miRNAs are differentially expressed in adipocytes and in subpopulations from the stromal vascular fraction. Finally, integration of transcriptomic data showed that bioinformatically predicted miRNA target genes rarely showed anticorrelated expression with that of targeting miRNA, in contrast to experimentally validated target genes.Taken together, our data indicate that the dysregulated expression of miRNAs occurs in distinct cell types and is likely to affect cell-specific function(s) of obese WAT.
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