Characterization of Micro-RNA Changes during the Progression of Type 2 Diabetes in Zucker Diabetic Fatty Rats

被引:53
作者
Delic, Denis [1 ]
Eisele, Claudia [1 ]
Schmid, Ramona [1 ]
Luippold, Gerd [2 ]
Mayoux, Eric [2 ]
Grempler, Rolf [1 ]
机构
[1] Boehringer Ingelheim Pharma GmbH & Co KG, Dept Translat Med & Clin Pharmacol, D-88397 Biberach, Germany
[2] Boehringer Ingelheim Pharma GmbH & Co KG, Dept CardioMetab Dis Res, D-88397 Biberach, Germany
关键词
ZDF rats; hyperinsulinemia; diabetes; micro-RNA; biomarker; disease progression; miR-122; miR-133a; miR-375; ACUTE MYOCARDIAL-INFARCTION; CIRCULATING MICRORNA; SKELETAL-MUSCLE; PCR DATA; NONCODING RNAS; CELL FUNCTION; BETA-CELLS; EXPRESSION; MIR-375; LIVER;
D O I
10.3390/ijms17050665
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the present pilot study was the identification of micro-RNA changes over time during the development and progression of type 2 diabetes (T2D) in Zucker diabetic fatty rats (ZDF rats). T2D is a complex metabolic disorder that is characterized, inter alia, by progressive failure of pancreatic beta cells to produce insulin, but also by functional or morphological modifications of others organ, such as liver, adipose tissue and the cardiovascular system. Micro-RNAs are a novel class of biomarkers that have the potential to represent biomarkers of disease progression. In this study, the onset and progression of diabetes was followed in ZDF rats from six weeks until 17 weeks of age. After an initial phase of hyperinsulinemia, the animals developed T2D and lost the capacity to produce sufficient insulin. Circulating miRNAs were measured from plasma samples at four time points: pre-diabetes (six weeks of age), hyperinsulinemia (eight weeks), beta cell failure (11 weeks) and late-stage diabetes (17 weeks) using TaqMan miRNA arrays. Bioinformatic analysis revealed distinct changes of circulating miRNAs over time. Several miRNAs were found to be increased over the course of the disease progression, such as miR-122, miR-133, miR-210 and miR-375. The most significantly decreased miRNAs were miR-140, miR-151-3p, miR-185, miR-203, miR-434-3p and miR-450a. Some of the miRNAs have also been identified in type 2 diabetic patients recently and, therefore, may have the potential to be useful biomarkers for the disease progression of T2D and/or the treatment response for anti-diabetic medications.
引用
收藏
页数:16
相关论文
共 69 条
  • [1] Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets
    Andersen, CL
    Jensen, JL
    Orntoft, TF
    [J]. CANCER RESEARCH, 2004, 64 (15) : 5245 - 5250
  • [2] [Anonymous], UK PROSP DIAB STUD 1
  • [3] Molecular Interplay between microRNA-34a and Sirtuin1 in Hyperglycemia-Mediated Impaired Angiogenesis in Endothelial Cells: Effects of Metformin
    Arunachalam, Gnanapragasam
    Lakshmanan, Arun Prasath
    Samuel, Samson Mathews
    Triggle, Chris R.
    Ding, Hong
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2016, 356 (02) : 314 - 323
  • [4] MicroRNA-29a is up-regulated in beta-cells by glucose and decreases glucose-stimulated insulin secretion
    Bagge, Annika
    Clausen, Trine R.
    Larsen, Sylvester
    Ladefoged, Mette
    Rosenstierne, Maiken W.
    Larsen, Louise
    Vang, Ole
    Nielsen, Jens H.
    Dalgaard, Louise T.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 426 (02) : 266 - 272
  • [5] MicroRNA-185 Targets SOCS3 to Inhibit Beta-Cell Dysfunction in Diabetes
    Bao, Lidao
    Fu, Xudong
    Si, Mingwen
    Wang, Yi
    Ma, Ruilian
    Ren, Xianhua
    Lv, Haijun
    [J]. PLOS ONE, 2015, 10 (02):
  • [6] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [7] Cardiac and renal function are progressively impaired with aging in Zucker diabetic fatty type II diabetic rats
    Baynes, John
    Murray, David B.
    [J]. OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2009, 2 (05) : 328 - 334
  • [8] Controlling the false discovery rate in behavior genetics research
    Benjamini, Y
    Drai, D
    Elmer, G
    Kafkafi, N
    Golani, I
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) : 279 - 284
  • [9] Influence of miRNA in insulin signaling pathway and insulin resistance: micro-molecules with a major role in type-2 diabetes
    Chakraborty, Chiranjib
    Doss, C. George Priya
    Bandyopadhyay, Sanghamitra
    Agoramoorthy, Govindasamy
    [J]. WILEY INTERDISCIPLINARY REVIEWS-RNA, 2014, 5 (05) : 697 - 712
  • [10] The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation
    Chen, JF
    Mandel, EM
    Thomson, JM
    Wu, QL
    Callis, TE
    Hammond, SM
    Conlon, FL
    Wang, DZ
    [J]. NATURE GENETICS, 2006, 38 (02) : 228 - 233