Increased Nuclear FOXP2 Is Related to Reduced Neural Stem Cell Number and Increased Neurogenesis in the Dorsal Telencephalon of Embryos of Diabetic Rats through Histamine H-1 Receptors

卷:12

Article

关键词: AUTISM SPECTRUM DISORDERS;    NEURONAL DIFFERENTIATION;    STEREOSELECTIVE PHARMACOKINETICS;    CORTICAL-NEURONS;    OXIDATIVE STRESS;    PROTEIN;    GENE;    CHLORPHENIRAMINE;    PROLIFERATION;    EXPRESSION;   

DOI  :  10.3390/cells12030510

来源: SCIE

【 摘 要 】

Diabetic rat embryos have increased cortical neurogenesis and neuron maturation, and their offspring presented altered neuron polarity, lamination, and diminished neuron excitability. The FOXP2 overexpression results in higher cortical neurogenesis by increasing the transition of radial glia to the intermediate progenitor. Similarly, histamine through H-1-receptor activation increases cortical neuron differentiation. Indeed, blocking the H-1-receptor by the systemic administration of chlorpheniramine to diabetic pregnant rats prevents increased neurogenesis. Here, we explore the relationship between the H-1-receptor and FOXP2 on embryo neurogenesis from diabetic dams. Through qRT-PCR, Western blot, immunohistofluorescence, and flow cytometry, we showed an increased FOXP2 expression and nuclear localization, a reduced Nestin expression and -positive cells number, and a higher PKC alpha expression in the cortical neuroepithelium of fourteen-day-old embryos from diabetic rats. Interestingly, this scenario was prevented by the chlorpheniramine systemic administration to diabetic pregnant rats at embryo day twelve. These data, together with the bioinformatic analysis, suggest that higher H-1-receptor activity in embryos under high glucose increases FOXP2 nuclear translocation, presumably through PKC alpha phosphorylation, impairing the transition of radial glia to intermediate progenitor and increasing neuron differentiation in embryos of diabetic rats.