NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo, and Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.
Division of Mental Health and Addiction, Møre and Romsdal Hospital Trust, Kristiansund, Norway.
Transl Psychiatry. 2018 Mar 6;8(1):55. doi: 10.1038/s41398-018-0102-1.
The Wnt signaling pathway plays a crucial role in neurodevelopment and in regulating the function and structure of the adult nervous system. Schizophrenia (SCZ) and bipolar disorder (BD) are severe mental disorders with evidence of subtle neurodevelopmental, structural and functional neuronal abnormalities. We aimed to elucidate the role of aberrant regulation of the Wnt system in these disorders by evaluating plasma levels of secreted Wnt modulators in patients (SCZ = 551 and BD = 246) and healthy controls (HCs = 639) using enzyme immune-assay. We also investigated the expression of 141 Wnt-related genes in whole blood in a subsample (SCZ = 338, BD = 241, and HCs = 263) using microarray analysis. Both SCZ and BD had dysregulated mRNA expression of Wnt-related genes favoring attenuated canonical (beta-catenin-dependent) signaling, and there were also indices of enhanced non-canonical Wnt signaling. In particular, FZD7, which may activate all Wnt pathways, but favors non-canonical signaling, and NFATc3, a downstream transcription factor and readout of the non-canonical Wnt/Ca pathway, were significantly increased in SCZ and BD (p < 3 × 10). Furthermore, patients had lower plasma levels of soluble dickkopf 1 and sclerostin (p < 0.01) compared with HC. Our findings suggest that SCZ and BD are characterized by abnormal Wnt gene expression and plasma protein levels, and we propose that drugs targeting the Wnt pathway may have a role in the treatment of severe mental disorders.
Wnt 信号通路在神经发育和调节成人神经系统的功能和结构中起着至关重要的作用。精神分裂症(SCZ)和双相情感障碍(BD)是严重的精神障碍,有证据表明存在微妙的神经发育、结构和功能神经元异常。我们旨在通过使用酶免疫测定法评估患者(SCZ=551 和 BD=246)和健康对照者(HCs=639)的血浆中分泌型 Wnt 调节剂水平,来阐明 Wnt 系统异常调节在这些疾病中的作用。我们还使用微阵列分析研究了全血中 141 个 Wnt 相关基因在亚样本中的表达(SCZ=338,BD=241 和 HCs=263)。SCZ 和 BD 均存在 Wnt 相关基因的 mRNA 表达失调,有利于减弱经典(β-连环蛋白依赖性)信号,并且还存在增强的非经典 Wnt 信号的指标。特别是 FZD7,它可能激活所有 Wnt 途径,但有利于非经典信号,以及 NFATc3,非经典 Wnt/Ca 途径的下游转录因子和读出物,在 SCZ 和 BD 中显著增加(p<3×10)。此外,与 HCs 相比,患者的可溶性 dickkopf 1 和 sclerostin 血浆水平较低(p<0.01)。我们的研究结果表明,SCZ 和 BD 的特征是异常的 Wnt 基因表达和血浆蛋白水平,我们提出靶向 Wnt 途径的药物可能在治疗严重精神障碍方面发挥作用。