University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, Level 4, Box 289, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK.
MRC Toxicology Unit, Hodgkin Building, PO Box 138, University of Leicester, Lancaster Road, Leicester LE1 9HN, UK.
Mol Metab. 2014 Jan 20;3(3):325-33. doi: 10.1016/j.molmet.2014.01.007. eCollection 2014 Jun.
We determined the effects of maternal diet-induced obesity on offspring adipose tissue insulin signalling and miRNA expression in the aetiology of insulin resistance in later life. Although body composition and glucose tolerance of 8-week-old male offspring of obese dams were not dysregulated, serum insulin was significantly (p<0.05) elevated. Key insulin signalling proteins in adipose tissue were down-regulated, including the insulin receptor, catalytic (p110β) and regulatory (p85α) subunits of PI3K as well as AKT1 and 2 (all p<0.05). The largest reduction observed was in IRS-1 protein (p<0.001), which was regulated post-transcriptionally. Concurrently, miR-126, which targets IRS-1, was up-regulated (p<0.05). These two features were maintained in isolated primary pre-adipocytes and differentiated adipocytes in-vitro. We have therefore established that maternal diet-induced obesity programs adipose tissue insulin resistance. We hypothesise that maintenance of the phenotype in-vitro strongly suggests that this mechanism is cell autonomous and may drive insulin resistance in later life.
我们确定了母体饮食诱导的肥胖对后代脂肪组织胰岛素信号和 miRNA 表达的影响,这些影响在胰岛素抵抗的发病机制中起着重要作用。尽管肥胖母鼠的 8 周龄雄性后代的身体成分和葡萄糖耐量没有失调,但血清胰岛素水平显著升高(p<0.05)。脂肪组织中关键的胰岛素信号蛋白下调,包括胰岛素受体、PI3K 的催化(p110β)和调节(p85α)亚基以及 AKT1 和 2(均 p<0.05)。观察到的最大减少是 IRS-1 蛋白(p<0.001),其受到转录后调控。同时,靶向 IRS-1 的 miR-126 也上调(p<0.05)。这两个特征在体外分离的原代前体脂肪细胞和分化的脂肪细胞中得以维持。因此,我们已经确定母体饮食诱导的肥胖会导致脂肪组织胰岛素抵抗。我们假设体外维持表型强烈表明这种机制是细胞自主的,可能导致后期生活中的胰岛素抵抗。