Jewell Christine M, Katen Kevin S, Barber Lisa M, Cannon Crystal, Garantziotis Stavros, Cidlowski John A
Signal Transduction Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina; and.
SRA International Inc., Durham, North Carolina.
Am J Physiol Endocrinol Metab. 2016 Oct 1;311(4):E741-E748. doi: 10.1152/ajpendo.00105.2016. Epub 2016 Sep 6.
The glucocorticoid receptor single-nucleotide polymorphism (SNP) N363S has been reported to be associated with metabolic syndrome, type 2 diabetes, and cardiovascular disease. Our aim was to determine how the N363S SNP modifies glucocorticoid receptor signaling in a healthy population of individuals prior to the onset of disease. We examined the function of the N363S SNP in a cohort of subjects from the general population of North Carolina. Eighteen N363S heterozygous carriers and 36 noncarrier, control subjects were examined for clinical and biochemical parameters followed by a low-dose dexamethasone suppression test to evaluate glucocorticoid responsiveness. Serum insulin measurements revealed that N363S carriers have higher levels of insulin, although not statistically significant, compared with controls. Glucocorticoid receptor protein levels evaluated in peripheral blood mononuclear cells from each clinical subject showed no difference between N363S and control. However, investigation of gene expression profiles in macrophages isolated from controls and N363S carriers using microarray, quantitative RT-PCR, and NanoString analyses revealed that the N363S SNP had an altered profile compared with control. These changes in gene expression occurred in both the absence and the presence of glucocorticoids. Thus, our observed difference in gene regulation between normal N363S SNP carriers and noncarrier controls may underlie the emergence of metabolic syndrome, type 2 diabetes, and cardiovascular disease associated with the N363S polymorphism.
据报道,糖皮质激素受体单核苷酸多态性(SNP)N363S与代谢综合征、2型糖尿病和心血管疾病有关。我们的目的是确定N363S SNP如何在疾病发作前的健康人群中改变糖皮质激素受体信号传导。我们在北卡罗来纳州普通人群的一组受试者中研究了N363S SNP的功能。对18名N363S杂合子携带者和36名非携带者对照受试者进行了临床和生化参数检查,随后进行低剂量地塞米松抑制试验以评估糖皮质激素反应性。血清胰岛素测量结果显示,与对照组相比,N363S携带者的胰岛素水平较高,尽管无统计学意义。对每个临床受试者外周血单核细胞中评估的糖皮质激素受体蛋白水平显示,N363S与对照组之间无差异。然而,使用微阵列、定量RT-PCR和NanoString分析对从对照组和N363S携带者中分离的巨噬细胞中的基因表达谱进行研究发现,与对照组相比,N363S SNP的表达谱发生了改变。这些基因表达的变化在糖皮质激素存在和不存在的情况下均会发生。因此,我们观察到的正常N363S SNP携带者与非携带者对照之间基因调控的差异可能是与N363S多态性相关的代谢综合征、2型糖尿病和心血管疾病出现的基础。