Huang Joanne H, Park Hyoungjun, Iaconelli Jonathan, Berkovitch Shaunna S, Watmuff Bradley, McPhie Donna, Öngür Dost, Cohen Bruce M, Clish Clary B, Karmacharya Rakesh
Center for Experimental Drugs and Diagnostics, Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Harvard Medical School and Massachusetts General Hospital , Boston, Massachusetts 02114, United States.
Chemical Biology Program, Broad Institute of Harvard and MIT , Cambridge, Massachusetts 02142, United States.
J Proteome Res. 2017 Feb 3;16(2):481-493. doi: 10.1021/acs.jproteome.6b00628. Epub 2016 Nov 28.
We undertook an unbiased metabolite profiling of fibroblasts from schizophrenia patients and healthy controls to identify metabolites and pathways that are dysregulated in disease, seeking to gain new insights into the disease biology of schizophrenia and to discover potential disease-related biomarkers. We measured polar and nonpolar metabolites in the fibroblasts under normal conditions and under two stressful physiological perturbations: growth in low-glucose media and exposure to the steroid hormone dexamethasone. We found that metabolites that were significantly different between schizophrenia and control subjects showed separation of the two groups by partial least-squares discriminant analysis methods. This separation between schizophrenia and healthy controls was more robust with metabolites identified under the perturbation conditions. The most significant individual metabolite differences were also found in the perturbation experiments. Metabolites that were significantly different between schizophrenia and healthy controls included a number of plasmalogens and phosphatidylcholines. We present these results in the context of previous reports of metabolic profiling of brain tissue and plasma in schizophrenia. These results show the applicability of metabolite profiling under stressful perturbations to reveal cellular pathways that may be involved in disease biology.
我们对精神分裂症患者和健康对照者的成纤维细胞进行了无偏代谢物谱分析,以鉴定疾病中失调的代谢物和途径,旨在深入了解精神分裂症的疾病生物学并发现潜在的疾病相关生物标志物。我们在正常条件下以及两种应激生理扰动下测量了成纤维细胞中的极性和非极性代谢物:在低葡萄糖培养基中生长以及暴露于类固醇激素地塞米松。我们发现,精神分裂症患者和对照受试者之间存在显著差异的代谢物通过偏最小二乘判别分析方法显示出两组的分离。在扰动条件下鉴定出的代谢物使精神分裂症患者和健康对照者之间的这种分离更为明显。在扰动实验中也发现了最显著的个体代谢物差异。精神分裂症患者和健康对照者之间存在显著差异的代谢物包括多种缩醛磷脂和磷脂酰胆碱。我们在先前关于精神分裂症脑组织和血浆代谢物谱分析报告的背景下展示了这些结果。这些结果表明,在应激扰动下进行代谢物谱分析可用于揭示可能参与疾病生物学的细胞途径。