Tan Paul, Pepin Émilie, Lavoie Julie L
Centre de Recherche du Centre Hospitalier, Université de Montréal; Department of Biochemistry and Molecular Medicine, Université de Montréal.
Centre de Recherche du Centre Hospitalier, Université de Montréal; Montreal Diabetes Research Center.
J Vis Exp. 2018 Jan 31(131):57026. doi: 10.3791/57026.
Compared to other tissues, white adipose tissue has a considerably less RNA and protein content for downstream applications such as real-time PCR and Western Blot, since it mostly contains lipids. RNA isolation from adipose tissue samples is also challenging as extra steps are required to avoid these lipids. Here, we present a procedure to collect three anatomically different white adipose tissues from mice, to process these samples and perform RNA isolation. We further describe the synthesis of cDNA and gene expression experiments using real-time PCR. The hereby described protocol allows the reduction of contamination from the animal's hair and blood on fat pads as well as cross-contamination between different fat pads during tissue collection. It has also been optimized to ensure adequate quantity and quality of the RNA extracted. This protocol can be widely applied to any mouse model where adipose tissue samples are required for routine experiments such as real-time PCR but is not intended for isolation from primary adipocytes cell culture.
与其他组织相比,白色脂肪组织的RNA和蛋白质含量要少得多,不利于进行实时PCR和蛋白质免疫印迹等下游应用,因为它主要含有脂质。从脂肪组织样本中分离RNA也具有挑战性,因为需要额外的步骤来避免这些脂质。在这里,我们展示了一种从小鼠身上收集三种解剖学上不同的白色脂肪组织、处理这些样本并进行RNA分离的方法。我们进一步描述了使用实时PCR进行cDNA合成和基因表达实验的过程。此处所述的方案可减少脂肪垫上动物毛发和血液的污染,以及组织收集过程中不同脂肪垫之间的交叉污染。它也经过优化,以确保提取的RNA有足够的量和质量。该方案可广泛应用于任何需要脂肪组织样本进行实时PCR等常规实验的小鼠模型,但不适用于从原代脂肪细胞培养物中分离。