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多器官样本代谢组学分析:MODY5/RCAD 突变小鼠的评估。

Metabolic Profiling of Multiorgan Samples: Evaluation of MODY5/RCAD Mutant Mice.

机构信息

Computational Life Science Cluster (CLiC), Department of Chemistry , Umeå University , Umeå 90187 , Sweden.

Accelerator Lab (ACL) , Karlsruhe Institute of Technology , Karlsruhe 76344 , Germany.

出版信息

J Proteome Res. 2018 Jul 6;17(7):2293-2306. doi: 10.1021/acs.jproteome.7b00821. Epub 2018 Jun 15.

Abstract

In the present study, we performed a metabolomics analysis to evaluate a MODY5/RCAD mouse mutant line as a potential model for HNF1B-associated diseases. Gas chromatography time-of-flight mass spectrometry (GC-TOF-MS) of gut, kidney, liver, muscle, pancreas, and plasma samples uncovered the tissue specific metabolite distribution. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) was used to identify the differences between MODY5/RCAD and wild-type mice in each of the tissues. The differences included, for example, increased levels of amino acids in the kidneys and reduced levels of fatty acids in the muscles of the MODY5/RCAD mice. Interestingly, campesterol was found in higher concentrations in the MODY5/RCAD mice, with a four-fold and three-fold increase in kidneys and pancreas, respectively. As expected, the MODY5/RCAD mice displayed signs of impaired renal function in addition to disturbed liver lipid metabolism, with increased lipid and fatty acid accumulation in the liver. From a metabolomics perspective, the MODY5/RCAD model was proven to display a metabolic pattern similar to what would be suspected in HNF1B-associated diseases. These findings were in line with the presumed outcome of the mutation based on the different anatomy and function of the tissues as well as the effect of the mutation on development.

摘要

在本研究中,我们进行了代谢组学分析,以评估 MODY5/RCAD 小鼠突变体作为 HNF1B 相关疾病潜在模型的适用性。对肠道、肾脏、肝脏、肌肉、胰腺和血浆样本进行气相色谱飞行时间质谱 (GC-TOF-MS) 分析,揭示了组织特异性代谢物分布。正交投影判别分析 (OPLS-DA) 用于鉴定 MODY5/RCAD 和野生型小鼠在每个组织中的差异。这些差异包括,例如,MODY5/RCAD 小鼠肾脏中的氨基酸水平升高,肌肉中的脂肪酸水平降低。有趣的是,MODY5/RCAD 小鼠中的菜油甾醇浓度更高,在肾脏和胰腺中分别增加了四倍和三倍。正如预期的那样,MODY5/RCAD 小鼠除了肝脏脂质代谢紊乱外,还出现了肾功能受损的迹象,肝脏中的脂质和脂肪酸积累增加。从代谢组学的角度来看,MODY5/RCAD 模型被证明显示出与 HNF1B 相关疾病中疑似的代谢模式相似。这些发现与基于组织不同的解剖结构和功能以及突变对发育的影响对突变的预期结果一致。

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