Ordelheide Anna-Maria, Heni Martin, Gommer Nadja, Gasse Lisa, Haas Carina, Guirguis Alke, Machicao Fausto, Häring Hans-Ulrich, Staiger Harald
Division of Endocrinology, Department of Internal Medicine, Eberhard Karls University Tübingen and German Center for Diabetes Research (DZD eV), Tübingen, Germany.
Exp Diabetes Res. 2011;2011:692536. doi: 10.1155/2011/692536. Epub 2011 Jan 27.
Muscle lipid oxidation is stimulated by peroxisome proliferator-activated receptor (PPAR) δ or adiponectin receptor signalling. We studied human myocyte expression of the PPARδ and adiponectin receptor genes and their relationship to lipid parameters of the donors. The mRNA levels of the three adiponectin receptors, AdipoR1, AdipoR2, and T-cadherin, were highly interrelated (r ≥ 0.91). However, they were not associated with GPBAR1, an unrelated membrane receptor. In addition, the adiponectin receptors were positively associated with PPARδ expression (r ≥ 0.75). However, they were not associated with PPARα. Using stepwise multiple linear regression analysis, PPARδ was a significant determinant of T-cadherin (P = .0002). However, pharmacological PPARδ activation did not increase T-cadherin expression. The myocyte expression levels of AdipoR1 and T-cadherin were inversely associated with the donors' fasting plasma triglycerides (P < .03). In conclusion, myocyte expression of PPARδ and the adiponectin receptors are highly coordinated, and this might be of relevance for human lipid metabolism in vivo.
肌肉脂质氧化受过氧化物酶体增殖物激活受体(PPAR)δ或脂联素受体信号传导的刺激。我们研究了人肌细胞中PPARδ和脂联素受体基因的表达及其与供体脂质参数的关系。三种脂联素受体AdipoR1、AdipoR2和T-钙黏蛋白的mRNA水平高度相关(r≥0.91)。然而,它们与不相关的膜受体GPBAR1无关。此外,脂联素受体与PPARδ表达呈正相关(r≥0.75)。然而,它们与PPARα无关。使用逐步多元线性回归分析,PPARδ是T-钙黏蛋白的重要决定因素(P = 0.0002)。然而,PPARδ的药理学激活并未增加T-钙黏蛋白的表达。AdipoR1和T-钙黏蛋白的肌细胞表达水平与供体的空腹血浆甘油三酯呈负相关(P < 0.03)。总之,PPARδ和脂联素受体的肌细胞表达高度协调,这可能与体内人类脂质代谢相关。