Graduate School of Regional Innovation Studies, Mie University, 1577 Kurimamachiya-cho, Tsu 514-8507, Japan.
Diabetol Metab Syndr. 2014 Jan 27;6(1):8. doi: 10.1186/1758-5996-6-8.
The etiology of the metabolic syndrome is complex, and is determined by the interplay of both genetic and environmental factors. The present study was designed to identify genes and proteins in the adipose tissues with altered expression in the spontaneously hypertensive/NIH -corpulent rat, SHR/NDmcr-cp (CP) and to find possible molecular targets associated with the pathogenesis or progression of obesity related to the metabolic syndrome.
We extracted RNAs and proteins from the epididymal adipose tissues in CP, SHR/Lean (Lean), and Wistar Kyoto (WKY) rats and performed microarray analysis and two-dimensional difference in gel electrophoresis (2D-DIGE) linked to a matrix-assisted laser desorption ionization time-of-flight tandem mass spectrometry (MALDI-TOF/TOF MS).
The results showed different mRNA and protein expression levels in the adipose tissue: oligo DNA microarray identified 33 genes that were significantly (P < 0.01) up-regulated and 17 genes significantly down-regulated in CP compared with WKY and Lean rats at both 6 and 25 weeks of age. The affected genes-proteins were associated with lipolytic enzymes stimulated by peroxisome proliferator-activated receptor (PPAR) signaling. Further analysis using the 2D-DIGE connected with MALDI-TOF/TOF analysis, the expression of monoglyceride lipase (MGLL) was significantly up-regulated and that of carboxylesterase 3 (CES3) was significantly down-regulated in 6- and 25-week-old CP compared with age-matched control (WKY and Lean rats).
Our results suggest the possible involvement of proteins associated with adipocyte lipolysis in obesity related to the metabolic syndrome.
代谢综合征的病因复杂,是由遗传和环境因素相互作用决定的。本研究旨在鉴定自发性高血压/ NIH -肥胖大鼠(SHR / NDmcr-cp,CP)脂肪组织中表达改变的基因和蛋白质,并寻找与肥胖相关代谢综合征发病机制或进展相关的可能分子靶点。
我们从 CP、SHR / Lean(Lean)和 Wistar Kyoto(WKY)大鼠的附睾脂肪组织中提取 RNA 和蛋白质,进行微阵列分析和二维差异凝胶电泳(2D-DIGE),并结合基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF MS)。
结果显示脂肪组织中存在不同的 mRNA 和蛋白质表达水平:寡 DNA 微阵列鉴定出 33 个基因,在 6 周和 25 周时 CP 与 WKY 和 Lean 大鼠相比显著上调(P < 0.01),17 个基因显著下调。受影响的基因-蛋白质与过氧化物酶体增殖物激活受体(PPAR)信号刺激的脂肪酶有关。使用与 MALDI-TOF/TOF 分析连接的 2D-DIGE 进一步分析,与年龄匹配的对照组(WKY 和 Lean 大鼠)相比,6 周和 25 周 CP 中单甘油酯脂肪酶(MGLL)的表达显著上调,羧酸酯酶 3(CES3)的表达显著下调。
我们的结果表明,与肥胖相关代谢综合征相关的脂肪细胞脂肪分解相关蛋白可能参与其中。