Malakauskas Sandra M, Kourany Wissam M, Zhang Xiao Yin, Lu Danhong, Stevens Robert D, Koves Timothy R, Hohmeier Hans E, Muoio Deborah M, Newgard Christopher B, Le Thu H
Department of Medicine, Duke University, Durham, North Carolina 27710, USA.
Mol Endocrinol. 2009 Jun;23(6):881-92. doi: 10.1210/me.2008-0274. Epub 2009 Feb 26.
Collectrin is a downstream target of the transcription factor hepatocyte nuclear factor-1alpha (HNF-1alpha), which is mutated in maturity-onset diabetes of the young subtype 3 (MODY3). Evidence from transgenic mouse models with collectrin overexpression in pancreatic islets suggests divergent roles for collectrin in influencing beta-cell mass and insulin exocytosis. To clarify the function of collectrin in the pancreas, we used a mouse line with targeted deletion of the gene. We examined pancreas morphology, glucose homeostasis by ip glucose tolerance testing (IPGTT) and insulin tolerance testing (IPITT), and pancreas function by in vivo acute-phase insulin response determination and glucose-stimulated insulin secretion from isolated islets. We find no difference in either pancreas morphology or function between wild-type and collectrin-deficient animals (Tmem27(-/y)). However, we note that by 6 months of age, Tmem27(-/y) mice exhibit increased insulin sensitivity by IPITT and decreased adiposity by dual-energy x-ray absorptiometry scanning compared with wild-type. We have previously reported that Tmem27(-/y) mice exhibit profound aminoaciduria due to failed renal recovery. We now demonstrate that Tmem27(-/y) animals also display inappropriate excretion of some short-chain acylcarnitines derived from amino acid and fatty acid oxidation. We provide further evidence for compensatory up-regulation of oxidative metabolism in Tmem27(-/y) mice, along with enhanced protein turnover associated with preserved lean mass even out to 1.5 yr of age. Our studies suggest that collectrin-deficient mice activate a number of adaptive mechanisms to defend energy homeostasis in the setting of ongoing nutrient losses.
Collectrin是转录因子肝细胞核因子-1α(HNF-1α)的下游靶点,该转录因子在青年型3型成年发病型糖尿病(MODY3)中发生突变。胰岛中过表达Collectrin的转基因小鼠模型的证据表明,Collectrin在影响β细胞质量和胰岛素胞吐作用方面具有不同的作用。为了阐明Collectrin在胰腺中的功能,我们使用了一个基因靶向缺失的小鼠品系。我们通过腹腔内葡萄糖耐量试验(IPGTT)和胰岛素耐量试验(IPITT)检测胰腺形态、葡萄糖稳态,并通过体内急性期胰岛素反应测定和分离胰岛的葡萄糖刺激胰岛素分泌检测胰腺功能。我们发现野生型和Collectrin缺陷型动物(Tmem27(-/y))在胰腺形态或功能上均无差异。然而,我们注意到,与野生型相比,到6个月大时,Tmem27(-/y)小鼠通过IPITT表现出胰岛素敏感性增加,通过双能X射线吸收法扫描显示肥胖程度降低。我们之前报道过,Tmem27(-/y)小鼠由于肾脏重吸收功能障碍而出现严重的氨基酸尿。我们现在证明,Tmem27(-/y)动物还表现出一些源自氨基酸和脂肪酸氧化的短链酰基肉碱排泄异常。我们为Tmem27(-/y)小鼠氧化代谢的代偿性上调提供了进一步证据,同时还证明了与维持瘦体重相关的蛋白质周转率增强,甚至在1.5岁时也是如此。我们的研究表明,Collectrin缺陷型小鼠在持续营养流失的情况下会激活多种适应性机制来维持能量稳态。