中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
SILAC-based quantitative proteomic analysis of the livers of spontaneous obese and diabetic rhesus monkeys

文献类型:期刊论文

作者Wang, Junlong1,2,3; Xu, Shimeng4; Gao, Jing5,6; Zhang, Linqiang1,3; Zhang, Zhiguo1,3; Yang, Wenhui7; Li, Yunhai1,3; Liao, Shasha1,3; Zhou, Hu5,6; Liu, Pingsheng4
刊名AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
出版日期2018-08
卷号315期号:2页码:E294-E306
关键词liver rhesus monkey stable isotope labeling with amino acids in cell culture-based quantitative proteomics spontaneous Type 2 diabetes
ISSN号0193-1849
DOI10.1152/ajpendo.00016.2018
文献子类Article
英文摘要Type 2 diabetes mellitus (T2DM) is a severe metabolic disorder that affects more than 10% of the population worldwide. Obesity is a major cause of insulin resistance and contributes to the development of T2DM. Liver is an essential metabolic organ that plays crucial roles in the pathogenesis of obesity and diabetes. However, the underlying mechanisms of liver in the transition of obesity to diabetes are not fully understood. The nonhuman primate rhesus monkey is an appropriate animal for research of human diseases. Here, we first screened and selected three individuals of spontaneously diabetic rhesus monkeys. Interestingly, the diabetic monkeys were obese with a high body mass index at the beginning, but gradually lost their body weight during one year of observation. Furthermore, we performed stable isotope labeling with amino acids in cell culture-based quantitative proteomics to identify proteins and signaling pathways with altered expression in the liver of obese and diabetic monkeys. In total, 3,509 proteins were identified and quantified, of which 185 proteins displayed an altered expression level. Gene ontology analysis revealed that the expression of proteins involved in fatty acids beta-oxidation and galactose metabolism was increased in obese monkeys; while proteins involved in oxidative phosphorylation and branched chain amino acid (BCAA) degradation were upregulated in diabetic monkeys. In addition, we observed mild apoptosis in the liver of diabetic monkeys, suggesting liver injury at the late onset of diabetes. Taken together, our liver proteomics may reveal a distinct metabolic transition from fatty acids beta-oxidation in obese monkey to BCAA degradation in diabetic monkeys.
WOS关键词NONALCOHOLIC-FATTY-LIVER ; HEPATIC INSULIN-RESISTANCE ; OXIDATIVE-PHOSPHORYLATION ; PROTEIN-KINASE ; SUPER-SILAC ; MITOCHONDRIAL DYSFUNCTION ; FASTING HYPERGLYCEMIA ; MACACA-MULATTA ; DISEASE ; ASSOCIATION
资助项目National Natural Science Foundation of China[U1402225] ; National Natural Science Foundation of China[U1702288] ; National Natural Science Foundation of China[31671230] ; National Natural Science Foundation of China[31460268] ; National Natural Science Foundation of China[81700520] ; Chinese Academy of Sciences[XDB13030600] ; Yunnan Natural Science Foundation[2017FA007] ; Yunnan Provincial Science and Technology Department[2014HB022] ; Yunnan Oversea High-Level Talent Program[2015HA039] ; Yunnan Oversea High-Level Talent Program[2015HA040]
WOS研究方向Endocrinology & Metabolism ; Physiology
语种英语
WOS记录号WOS:000441173000017
出版者AMER PHYSIOLOGICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/279642]  
专题分析化学研究室
通讯作者Liang, Bin
作者单位1.Chinese Acad Sci, Ctr Excellence Anim Evolut & Genet, Kunming, Yunnan, Peoples R China;
2.Soochow Univ, Coll Pharmaceut Sci, Suzhou, Peoples R China;
3.Chinese Acad Sci, Chinese Acad Sci & Yunnan Prov, Key Lab Anim Models & Human Dis Mech, Kunming Inst Zool, Kunming, Yunnan, Peoples R China;
4.Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromolecules, Beijing, Peoples R China;
5.Chinese Acad Sci, Shanghai Inst Materia Med, Dept Analyt Chem, Shanghai, Peoples R China;
6.Chinese Acad Sci, Shanghai Inst Materia Med, CAS Key Lab Receptor Res, Shanghai, Peoples R China;
7.Kuruning Med Univ, Yanan Affiliated Hosp, Dept Geriatr, Key Lab Cardiovasc Dis Yunnan Prov, Kunming, Yunnan, Peoples R China
推荐引用方式
GB/T 7714
Wang, Junlong,Xu, Shimeng,Gao, Jing,et al. SILAC-based quantitative proteomic analysis of the livers of spontaneous obese and diabetic rhesus monkeys[J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM,2018,315(2):E294-E306.
APA Wang, Junlong.,Xu, Shimeng.,Gao, Jing.,Zhang, Linqiang.,Zhang, Zhiguo.,...&Liang, Bin.(2018).SILAC-based quantitative proteomic analysis of the livers of spontaneous obese and diabetic rhesus monkeys.AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM,315(2),E294-E306.
MLA Wang, Junlong,et al."SILAC-based quantitative proteomic analysis of the livers of spontaneous obese and diabetic rhesus monkeys".AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM 315.2(2018):E294-E306.

入库方式: OAI收割

来源:上海药物研究所

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