Polymorphisms in the hypoxia inducible factor binding site of the macrophage migration inhibitory factor gene promoter in schizophrenia

• Published in: PloS one 2022-03, Vol.17 (3), p.e0265738-e0265738
• Main Authors: Okazaki, Satoshi, Boku, Shuken, Watanabe, Yuichiro, Otsuka, Ikuo, Horai, Tadasu, Morikawa, Ryo, Kimura, Atsushi, Shimmyo, Naofumi, Tanifuji, Takaki, Someya, Toshiyuki, Hishimoto, Akitoyo
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Astrocytes; Binding Sites; Biology and Life Sciences; Biomarkers; Cytokines; Diagnosis; Environmental risk; Forebrain; Gene deletion; Gene expression; Genetic aspects; Genetic testing; Humans; Hypoxia; Hypoxia - genetics; Hypoxia-Inducible Factor 1, alpha Subunit - genetics; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism; Identification and classification; Leukocyte migration; Macrophage migration inhibitory factor; Macrophage Migration-Inhibitory Factors - genetics; Macrophage Migration-Inhibitory Factors - metabolism; Medicine; Medicine and Health Sciences; Mental disorders; Mice; Microsatellites; Migration; Migration inhibitory factor; Mutation; Neonates; Neurogenesis; Neuroprotection; Nucleotides; Pathophysiology; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Promoters (Genetics); Psychiatry; Psychotropic drugs; Regulatory sequences; Research and Analysis Methods; Risk analysis; Risk factors; Schizophrenia; Schizophrenia - genetics; Single nucleotide polymorphisms; Single-nucleotide polymorphism; University graduates
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0265738

Macrophage migration inhibitory factor (MIF) is a multifunctional cytokine that promotes neurogenesis and neuroprotection. MIF is predominantly expressed in astrocytes in the brain. The serum MIF level and microsatellites/single nucleotide polymorphisms (SNPs) in the MIF gene promoter region are known to be associated with schizophrenia (SCZ). Interestingly, previous studies reported that hypoxia, an environmental risk factor for SCZ, induced MIF expression through binding of the hypoxia inducible factor (HIF)-1 to the hypoxia response element (HRE) in the MIF promoter. We investigated the involvement of MIF in SCZ while focusing on the HIF pathway. First, we conducted an association study of the SNP rs17004038 (C>A) in the HRE of the MIF promoter between 1758 patients with SCZ and 1507 controls. Next, we investigated the effect of hypoxia on MIF expression in primary cultured astrocytes derived from neonatal mice forebrain. SNP rs17004038 was significantly associated with SCZ (p = 0.0424, odds ratio = 1.445), indicating that this SNP in the HRE of the MIF promoter was a genetic risk factor for SCZ. Hypoxia induced MIF mRNA expression and MIF protein production and increased HIF-1 binding to the MIF promoter, while the activity of the MIF promoter was suppressed by mutations in the HRE and by deletion of the HRE in astrocytes. These results suggest that SNP rs17004038 in the HRE of the MIF promoter was significantly associated with SCZ and may be involved in the pathophysiology of SCZ via suppression of hypoxia and HIF pathway-induced MIF expression.