Polysialylation in a DISC1 Mutant Mouse.
Yuka TakahashiChikara AbeMasaya HaneDi WuKen KitajimaChihiro SatoPublished in: International journal of molecular sciences (2022)
Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic (G) and environmental (E) factors. Polysialylation represents a unique posttranslational modification of a protein, and such changes in neural cell adhesion molecules (NCAMs) have been reported in postmortem brains from patients with psychiatric disorders. To understand the G × E effect on polysialylated NCAM expression, in this study, we performed precise measurements of polySia and NCAM using a disrupted-in-schizophrenia 1 (DISC1)-mutant mouse (G), a mouse model of schizophrenia, under acute stress conditions (E). This is the first study to reveal a lower number and smaller length of polySia in the suprachiasmatic nucleus of DISC1 mutants relative to those in wild-type (WT) mice. In addition, an analysis of polySia and NCAM responses to acute stress in five brain regions (olfactory bulb, prefrontal cortex, suprachiasmatic nucleus, amygdala, and hippocampus) revealed that the pattern of changes in these responses in WT mice and DISC1 mutants differed by region. These differences could indicate the vulnerability of DISC1 mutants to stress.
Keyphrases
- wild type
- prefrontal cortex
- bipolar disorder
- mouse model
- liver failure
- cell adhesion
- mental health
- end stage renal disease
- resting state
- healthcare
- newly diagnosed
- chronic kidney disease
- genome wide
- functional connectivity
- stress induced
- climate change
- poor prognosis
- drug induced
- respiratory failure
- type diabetes
- prognostic factors
- multiple sclerosis
- cognitive impairment
- metabolic syndrome
- heat stress
- aortic dissection
- cerebral ischemia
- white matter