Expression of microRNA during bovine adipogenesis

S. L. Pratt, T. Burns, E. Curry, S. Duckett
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引用次数: 15

Abstract

Studies have recently indicated that the adipogenic process and the expression of genes involved in lipid metabolism may be regulated in part at the post-transcriptional level by a class of small RNA called microRNA (miRNA). The objectives of this study were to i) determine if miRNAs are differentially expressed, and ii) evaluate expression of known miRNA targets in bovine adipocytes. Bovine adipose samples were collected from castrated males fattened on a high concentrate diet (C) or pasture (PA) and were frozen in liquid nitrogen and stored at -80°C, or used to generate primary stromal-vascular cells (SV). SV cells were cultured to confluence (Control) or differentiated at confluence and harvested 2 (D2), 6 (D6), or 12 (D12) days post-confluence. A 3x3 microarray analysis was performed comparing Control and differentiated samples. miR-21, -221, and -222 (P less than 0.05) were differentially expressed. qRT-PCR was conducted using the in vitro samples, and all three miRNAs were down regulated on D2 (P less than 0.05). miR-221 and -222 were decreased on D6 compared to Control (P less than 0.05), but only miR-222 expression was decreased at D12 (P less than 0.05) compared to Control. miR-21 increased in expression compared to Control on D12 (P less than 0.05). In vivo , only miR-21 expression was affected and it was reduced in PA compared to C fat samples (P less than 0.05). Two targets of miR-21 are Programmed Cell Death Protein 4 (PDCD4) and Phosphatase and Tensin Homolog (PTEN), and neither messenger RNA was differentially expressed in vitro (P greater than 0.05), but both messenger RNAs were elevated for PA compared to C (P less than 0.05). These data show that miRNAs are differentially expressed in adipose cells and tissue, and that miR-21 may be involved in adipocyte function by regulating the translation of PDCD4 and PTEN.
牛脂肪形成过程中microRNA的表达
最近的研究表明,脂肪的形成过程和脂质代谢相关基因的表达可能在转录后水平部分受到一类被称为microRNA (miRNA)的小RNA的调控。本研究的目的是i)确定miRNA是否存在差异表达,ii)评估牛脂肪细胞中已知miRNA靶点的表达。从饲喂高精料日粮(C)或牧场(PA)的去势公牛中收集脂肪样本,在液氮中冷冻并在-80°C保存,或用于生成初级基质血管细胞(SV)。将SV细胞培养到融合(对照组)或在融合中分化,并在融合后2 (D2)、6 (D6)或12 (D12)天收获。对照和分化样品进行3x3微阵列分析。miR-21、-221、-222表达差异(P < 0.05)。体外样本进行qRT-PCR检测,3种mirna在D2上均下调(P < 0.05)。与对照组相比,D6时miR-221和-222表达降低(P < 0.05),而D12时仅miR-222表达降低(P < 0.05)。D12时miR-21表达较对照组升高(P < 0.05)。在体内,只有miR-21的表达受到影响,与C脂肪样品相比,PA中的miR-21表达降低(P < 0.05)。miR-21的两个靶点是程序性细胞死亡蛋白4 (PDCD4)和磷酸酶与紧张素同源物(PTEN),两种信使RNA在体外均无差异表达(P > 0.05),但两种信使RNA在PA中的表达均高于C (P < 0.05)。这些数据表明,mirna在脂肪细胞和组织中存在差异表达,miR-21可能通过调节PDCD4和PTEN的翻译参与脂肪细胞功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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