Lieberman Richard, Kranzler Henry R, Levine Eric S, Covault Jonathan
Alcohol Research Center, Department of Psychiatry, University of Connecticut School of Medicine, Farmington 06030-1410, CT, USA.
Center for Studies of Addiction, Department of Psychiatry, Perelman School of Medicine of the University of Pennsylvania, Philadelphia 19104, PA, USA; VISN4 MIRECC, Crescenz Philadelphia VAMC, Philadelphia 19104, PA, USA.
Psychiatry Res. 2017 Jan;247:172-181. doi: 10.1016/j.psychres.2016.11.027. Epub 2016 Nov 24.
In peripheral blood leukocytes, FKBP5 mRNA expression is upregulated following glucocorticoid receptor activation. The single nucleotide polymorphism rs1360780 in FKBP5 is associated with psychiatric illness and has functional molecular effects. However, examination of FKBP5 regulation has largely been limited to peripheral cells, which may not reflect regulation in neural cells. We used 27 human induced pluripotent stem cell lines (iPSCs) derived from 20 subjects to examine FKBP5 mRNA expression following GR activation. Following differentiation into forebrain-lineage neural cultures, cells were exposed to 1μM dexamethasone and mRNA expression of FKBP5 and NR3C1 analyzed. Results from the iPSC-derived neural cells were compared with those from 15 donor matched fibroblast lines. Following dexamethasone treatment, there was a 670% increase in FKBP5 expression in fibroblasts, mimicking findings in peripheral blood-derived cells, but only a 23% increase in iPSC-derived neural cultures. FKBP5 rs1360780 genotype did not affect the induction of FKBP5 mRNA in either fibroblasts or neural cells. These results suggest that iPSC-derived forebrain-lineage neurons may not be an optimal neural cell type in which to examine relationships between GR activation, FKBP5 expression, and genetic variation in human subjects. Further, FKBP5 induction following GR activation may differ between cell types derived from the same individual.
在外周血白细胞中,糖皮质激素受体激活后FKBP5信使核糖核酸(mRNA)表达上调。FKBP5中的单核苷酸多态性rs1360780与精神疾病相关,且具有功能性分子效应。然而,对FKBP5调控的研究主要局限于外周细胞,这可能无法反映神经细胞中的调控情况。我们使用了来自20名受试者的27个人诱导多能干细胞系(iPSC)来检测糖皮质激素受体(GR)激活后FKBP5 mRNA的表达。在分化为前脑谱系神经培养物后,将细胞暴露于1μM地塞米松,并分析FKBP5和NR3C1的mRNA表达。将iPSC来源的神经细胞的结果与15个供体匹配的成纤维细胞系的结果进行比较。地塞米松处理后,成纤维细胞中FKBP5的表达增加了670%,这与外周血来源细胞中的发现相似,但iPSC来源的神经培养物中仅增加了23%。FKBP5 rs1360780基因型在成纤维细胞或神经细胞中均不影响FKBP5 mRNA的诱导。这些结果表明,iPSC来源的前脑谱系神经元可能不是研究人类受试者中GR激活、FKBP5表达和基因变异之间关系的最佳神经细胞类型。此外,GR激活后FKBP5的诱导在来自同一个体的不同细胞类型之间可能存在差异。